Loading...

Table of Content

    26 January 2026, Volume 42 Issue 1
    Research Progress in Flavin Monooxygenases in Plants
    GAN Chen-lu, YOU Yu-ting, XIE Han-dan, ZENG Zi-xian, ZHU Bo
    2026, 42(1):  1-12.  doi:10.13560/j.cnki.biotech.bull.1985.2025-0953
    Asbtract ( 188 )   HTML ( 4)   PDF (1478KB) ( 64 )  
    Figures and Tables | References | Related Articles | Metrics

    Flavin monooxygenases (FMOs) are a class of flavin adenine dinucleotide (FAD)-dependent oxidoreductases that catalyze the oxidation of diverse substrates and play vital roles in plant metabolic regulation and environmental adaptation. The plant FMOs superfamily comprises multiple functional subfamilies, among which FMO1, YUCCAs, and FMOGS-OXs are most representative, functioning in immune defense, auxin biosynthesis, secondary metabolism, and stress responses. This review summarizes the structural features, evolutionary diversification, and functional mechanisms of these three subfamilies, and highlights recent advances in their roles in plant growth, development, and stress adaptation. FMOs generally contain conserved FAD/NADPH-binding domains and have undergone gene expansion during evolution, conferring functional diversification as well as pronounced redundancy and pleiotropy. Nevertheless, the natural substrate spectrum of most FMOs remains unresolved, and the molecular mechanisms driving their gene expansion and evolutionary diversification are yet to be elucidated. Moreover, their spatiotemporal specificity together with functional redundancy severely constrains in-depth mechanistic and applied research. Considering future, the integration of metabolomics, spatial omics, and artificial intelligence is expected to open new avenues for functional characterization and translational applications of FMOs, providing promising targets for molecular design breeding aimed at enhancing crop stress tolerance and yield improvement.

    Biological Functions and Regulatory Network of SLR1, a Negative Regulator of Gibberellin Signaling in Rice
    FEI Si-tian, HOU Ying-xiang, LI Lan, ZHANG Chao
    2026, 42(1):  13-30.  doi:10.13560/j.cnki.biotech.bull.1985.2025-0643
    Asbtract ( 578 )   HTML ( 4)   PDF (1280KB) ( 52 )  
    Figures and Tables | References | Related Articles | Metrics

    Gibberellins (GAs) are a class of important regulatory hormones in plants, widely involved in various life processes such as plant growth and development, and responses to stress. The regulation of GA biosynthesis and signaling pathways contributed to the first green revolution in crop breeding. SLR1 is the only DELLA protein in rice, serving as a key negative regulator in the GA signal transduction pathway that represses downstream GA signal transduction. SLR1 also participates in hormone pathways such as abscisic acid (ABA), jasmonic acid (JA), brassinosteroid (BR), and strigolactone (SL), acting as a "molecular bridge" for plant hormone crosstalk. However, the SLR1 protein lacks a typical DNA-binding domain, and there is currently no evidence indicating its ability to directly bind to DNA sequences. It mainly exerts its modulatory functions by interacting with other transcription factors to inhibit or activate the expressions of downstream genes. In addition, the expression and function of SLR1 itself are also subject to multiple regulations. At the transcriptional level, the SLR1 gene is negatively regulated by transcription factors such as OsYABBY4 and OsWRKY36; at the protein level, SLR1 undergoes modifications including ubiquitination, glycosylation, SUMOylation, and phosphorylation, as well as regulation of its own stability and activity through interactions with other proteins. SLR1 not only extensively regulates various growth and development processes but also participates responses to multiple biotic and abiotic stresses in rice, playing an important role throughout the entire growth cycle of rice. Recent research has revealed the great potential of SLR1 in breeding: regulating the protein abundance of SLR1 in rice and maintaining it at a moderate level is of great significance for improving rice tolerance to alkali and heat stress. This article mainly reviews the molecular structure and mechanism of action of SLR1, its crosstalk role in various plant hormone pathways, the protein modifications and regulations of SLR1 itself, as well as its specific biological functions. It aims to further explore SLR1-associated components and regulatory networks, providing references for rice molecular design breeding.

    Research Advances in Plant Extracts with Antiviral Activity against Bovine Viral Diarrhea Virus
    GAO Zheng, YIN Liu-yi, MENG Ling-pin, WANG Xiao-hui, SUN Jia-xin, SONG Yang, WEN Shu-bo
    2026, 42(1):  31-41.  doi:10.13560/j.cnki.biotech.bull.1985.2025-0523
    Asbtract ( 112 )   HTML ( 0)   PDF (991KB) ( 24 )  
    Figures and Tables | References | Related Articles | Metrics

    Bovine Viral Diarrhea Virus (BVDV) is the primary etiological agent of Bovine Viral Diarrhea-Mucosal Disease (BVD-MD), causing clinical manifestations such as fever, erosive and necrotic lesions of the oral and gastrointestinal mucosa, diarrhea, abortion in pregnant cows, fetal malformations, thrombocytopenia, leukopenia, and immunosuppression in calves. These symptoms impair herd health and cause significant economic losses, hindering the healthy and sustainable development of the cattle industry. Currently, vaccination and herd purification are the primary control measures; however, the limited protective efficacy of vaccines and the complexity and high cost of herd eradication programs pose significant challenges for implementation. Consequently, the development of safe and effective antiviral drugs as a complementary strategy is essential. However, no specific anti-BVDV therapeutics are available, significantly impeding disease control in production settings. In recent years, with advances in antiviral drug research, natural plant extracts have emerged as a promising resource for antiviral drug development due to their widespread availability, safety, efficacy, and multifaceted mechanisms. This review systematically summarizes recent progress in anti-BVDV plant extracts, focusing on their molecular targets and mechanisms, particularly their ability to exert antiviral effects through viral neutralization, suppression of viral replication, modulation of host immune responses, and alleviation of oxidative stress. These findings provide a robust scientific foundation for developing natural plant extracts as anti-BVDV therapeutics, highlighting their unique advantages in antiviral applications, and offer prospects and recommendations for future research.

    The Role of RNA-specific Adenosine Deaminase 1 in Innate Immunity and Inflammation
    LI Hui-hui, WANG Shu-jie, KANG Xiao-long
    2026, 42(1):  42-50.  doi:10.13560/j.cnki.biotech.bull.1985.2025-0608
    Asbtract ( 126 )   HTML ( 0)   PDF (1595KB) ( 14 )  
    Figures and Tables | References | Related Articles | Metrics

    RNA-specific adenosine deaminase 1 (ADAR1) is one of the key enzymes in RNA editing, capable of catalyzing the conversion of adenosine (A) in double-stranded RNA (dsRNA) molecules to inosine (I), and plays a significant role in physiological processes such as immune regulation and inflammatory responses. The immune regulatory effect of ADAR1 is reflected in a dual mechanism. Firstly, it modifies the structure of dsRNA through RNA editing to prevent it from activating pattern recognition receptors and downstream effector proteins, thereby maintaining autoimmune tolerance. Secondly, by interacting with pattern recognition receptors such as RIG-I and MDA5 in a non-editing-dependent manner, it indirectly regulates the activation of signaling molecules such as NF-κB and IRF, thereby affecting the release of pro-inflammatory cytokines. In the inflammatory response, ADAR1 exerts anti-inflammatory effects through multiple pathways. On the one hand, it can edit viral or endogenous dsRNA, reducing the activation ability of dsRNA for RIG-I and MDA5, thereby inhibiting the excessive activation of antiviral inflammation. On the other hand, ADAR1 interacts directly with PKR to inhibit the phosphorylation of eIF2α, thereby balancing cell survival and inflammatory death. Meanwhile, ADAR1 can also edit endogenous dsRNA to block abnormal RNA degradation in the OAS-RNase L pathway and avoid autoinflammation triggered thereby. Furthermore, ADAR1 competes with ZBP1 for binding to Z-RNA, inhibiting RIPK3-MLKL-mediated programmed necrosis, thereby alleviating the inflammatory response caused by necrosis. These mechanisms provide a theoretical basis for the development of therapeutic strategies for inflammatory diseases. However, most of the above-mentioned studies have focused on human and mouse models, and their regulatory roles in inflammatory diseases in domestic animals remain unclear. Given the significant impact of inflammatory diseases on the livestock economy, this paper reviews the research on ADAR1 in terms of inflammation and immunity, and summarizes its important regulatory mechanisms, with the aim of laying the foundation for revealing the pathogenesis of inflammatory diseases in domestic animals such as mastitis in dairy cows and developing effective prevention and treatment strategies.

    Advances in Artificial Intelligence for DNA Design
    LIU Huan, GUO Fa-xu, ZHAO Xiao-yan, HUANG Long-yu, WANG Jian, ZHOU Guo-min, ZHANG Jian-hua
    2026, 42(1):  51-66.  doi:10.13560/j.cnki.biotech.bull.1985.2025-0863
    Asbtract ( 131 )   HTML ( 0)   PDF (3117KB) ( 21 )  
    Figures and Tables | References | Related Articles | Metrics

    DNA design, namely the targeted construction and optimization of genomic functional elements to meet specific performance requirements, has become a core enabling technology at the forefront of synthetic biology and precision breeding. Traditional design approaches are constrained by limited understanding of complex regulatory networks and the vastness of the sequence search space, making efficient and precise sequence innovation difficult. In recent years, artificial intelligence (AI), especially the integrated use of deep generative and predictive models, has been reshaping the theoretical foundations and technical paradigms of DNA design. By learning the "regulatory grammar" embedded in massive omics datasets, these methods enable high-resolution functional prediction, multimodal data integration, and condition-controlled sequence generation within ultra-long genomic contexts. This article systematically reviews cutting-edge advances in AI for DNA design, with an emphasis on key technical pathways and applications of deep generative and predictive models in the design of multi-level regulatory elements such as promoters and enhancers, sequence optimization, and crop breeding. By establishing an intelligent closed loop of “design–prediction–optimization–validation”, AI not only markedly improves the efficiency and accuracy of designing complex functional elements, but also gives rise to synthetic sequences that outperform their natural counterparts. Looking ahead, as AI further converges with synthetic biology and experimental automation, DNA design is poised to achieve a full pipeline from intelligent design to high-throughput experimental validation, thereby accelerating breakthroughs in basic life science research and modern agricultural breeding.

    Preparation and Identification of Monoclonal Antibodies against the Bovine Coronavirus
    LIU Yu, LIU Xiao-xiao, ZHENG Jian-hao, LI Bin, HE Hong-hong, MAO Li
    2026, 42(1):  67-75.  doi:10.13560/j.cnki.biotech.bull.1985.2025-0838
    Asbtract ( 99 )   HTML ( 0)   PDF (7284KB) ( 29 )  
    Figures and Tables | References | Related Articles | Metrics

    Objective Bovine coronavirus (BCoV) is a major pathogen causing diarrhea in calves and winter dysentery in adult cattle, and respiratory diseases in cattle of all ages. The diseases caused by BCoV are widespread and lead to serious harm in the livestock industry. There are limitations in traditional diagnostic and control methods. The development of BCoV-specific monoclonal antibodies aims to facilitate precise diagnostic detection and provide critical experimental materials for coronavirus research. Method BALB/c mice were immunized with purified virus, and hybridoma cells were prepared using cell fusion technology. Monoclonal cell lines stably secreting specific antibodies were screened. The monoclonal antibodies were identified and subclassified by indirect immunofluorescence assay (IFA) and indirect enzyme-linked immunosorbent assay (ELISA). Concurrently the eukaryotic expression plasmids for the full-length S protein and S1, S2 subunits of cpCoV were constructed and then transfected into 293T cells. The viral proteins recognized by monoclonal antibodies were identified by IFA and Western-blot techniques. Result Monoclonal antibody 1E1 was successfully obtained through monoclonal screening. The ascites titer of antibody was >1∶81 000, and the subtype was identified as IgG1. The antibody specifically reacted with both BCoV and cpCoV. Through gene cloning and eukaryotic expression, it was verified that the antigenic epitopes recognized by 1E1 antibody were located in the S1 domain of the S protein. Conclusion By preparing BCoV monoclonal antibodies, the obtained monoclonal antibody 1E1 can be used for identification of both BCoV and cpCoV. The antigenic epitopes recognized by the antibody are verified, and analysis reveals that the homology of S1 protein sequence is 95.4%-99.6%, and has significant differences between BCoV and cpCoV. The result provides a new method for the detection of the two coronaviruses and a new tool for the basic research of BCoV and cpCoV.

    Multi-strategy Synergy Enhances the Diffraction Resolution of Protein Crystals
    REN Hong-yu, PANG Cui-ping, GU Yang, ZHOU Jia-hai
    2026, 42(1):  76-85.  doi:10.13560/j.cnki.biotech.bull.1985.2025-0975
    Asbtract ( 101 )   HTML ( 1)   PDF (2724KB) ( 22 )  
    Figures and Tables | References | Related Articles | Metrics

    Objective Protein crystallographic diffraction is an essential technique in structural biology research. The diffraction resolution of crystals directly determines the accuracy of atomic models and their practical applicability. Therefore, a combination of multiple strategies is required to optimize protein crystallization quality and enhance diffraction resolution. Method The P450 enzyme, which catalyzes aryl coupling reactions, was chosen as the research focus. A prokaryotic expression system was first constructed via molecular biology techniques. The protein was purified using nickel-affinity chromatography and size-exclusion chromatography. During the crystallization stage, 1,632 initial conditions were systematically screened through the vapor diffusion method. Based on preliminary results, key variables including buffer pH, precipitant type and concentration were finely optimized, and various additives were introduced to improve the crystallization environment. Furthermore, rational truncation of flexible regions was designed according to structural predictions, and SUMO tag fusion was attempted to enhance protein stability. Result The P450 protein was successfully expressed solubly at high levels in E. coli and purified to high purity via a two-step purification process, making it suitable for crystallization screening. Through large-scale crystallization condition screening and multiple rounds of optimization, combined with synergistic strategies including sequence truncation and SUMO fusion, crystal morphology was significantly improved—transitioning from initial microcrystals or amorphous precipitates to well-defined single crystals with regular shapes and sharp edges. The diffraction resolution of the crystals was markedly enhanced from an initial 10 Å to 2.86 Å, yielding high-quality crystals suitable for high-resolution structural analysis. Conclusion By employing a multi-strategy synergy, the protein crystal morphology and diffraction resolution of protein crystals is significantly enhanced.

    Expression and Functional Analysis of OsMATE34 in Rice under Mercury Stress
    YANG Yue-qin, XING Ying, ZHONG Zi-he, TIAN Wei-jun, YANG Xue-qing, WANG Jian-xu
    2026, 42(1):  86-94.  doi:10.13560/j.cnki.biotech.bull.1985.2025-0542
    Asbtract ( 700 )   HTML ( 2)   PDF (2395KB) ( 24 )  
    Figures and Tables | References | Related Articles | Metrics

    Objective The multidrug and toxic compound extrusion transporter (MATE) plays a significant regulatory role in plant nutrient absorption, secondary metabolite transport, and detoxification of heavy metals and exogenous substances. Studying biological function of OsMATE34 in rice (Oryza sativa) may lay a foundation for a deeper understanding of the molecular mechanisms underlying MeHg accumulation in rice, and provide scientific reference for the breeding of low-MeHg rice varieties. Method Bioinformatics tools were used to analyze the physicochemical properties and phylogenetic tree of OsMATE34. Real-time quantitative PCR (RT-qPCR) was used to detect the relative expressions of OsMATE34 in different rice tissues under MeHg stress. The MeHg contents in different tissues of rice after MeHg exposure were measured, and the correlation between gene expressions and MeHg content was analyzed. A CRISPR/Cas9-mediated OsMATE34 knockout line was generated, and MeHg treatment was performed on seedlings. The MeHg contents in wild-type (WT) and osmate34 rice lines were measured to explore the effects of OsMATE34 on MeHg absorption and transport. Result The OsMATE34 gene was located on chromosome 8, encoding a protein of 489 amino acids with a relative molecular weight of 51.60 kD and a theoretical isoelectric point (pI) of 5.6. The protein was hydrophobic. RT-qPCR showed that MeHg stress inhibited the expression of OsMATE34 in roots, The expressions of OsMATE34 in the leaf sheath and leaves were significantly up-regulated with the increase of MeHg concentration, and the gene expression in stems was 20-fold higher than that of the control when treated with 80 nmol/L MeHg. The MeHg contents in rice tissues increased under MeHg stress, with the root accumulating significantly higher MeHg than the leaf sheath and leaf. There was a significant positive correlation between OsMATE34 gene expression and MeHg content in rice leaf sheath and leaves with the increase of MeHg concentration. Compared to the wild-type, the OsMATE34 knockout lines showed a significant reduction in MeHg content in the leaf sheath, leaf, and xylem, while there was no significant difference in the root. Conclusion The OsMATE34 gene is involved in the transport of MeHg from the root to the aboveground tissues. This study provides a foundation for further research on the molecular mechanisms of MeHg absorption and transport in rice.

    Cloning and Functional Analysis of the Soybean Enoyl-CoA Reductase ECR14 Gene
    ZHANG Yue, DAI Yue-hua, ZHANG Ying-ying, LI Ao-hui, LI Chu-hui, XUE Jin-ai, QIN Hui-bin, CHEN Yan, NIE Meng-en, ZHANG Hai-ping
    2026, 42(1):  95-104.  doi:10.13560/j.cnki.biotech.bull.1985.2025-0493
    Asbtract ( 105 )   HTML ( 0)   PDF (2571KB) ( 13 )  
    Figures and Tables | References | Related Articles | Metrics

    Objective The ECR gene is a key one in the cuticular wax biosynthesis pathway of soybean plants. This study aims to investigate the biological function of the soybean GmECR14 gene, provide a theoretical basis for further exploring its molecular mechanism, and offer references for breeding new soybean varieties with high quality and stress tolerance. Method PCR technology was used to clone the GmECR14 gene the soybean cultivar ‘Jack’ . Bioinformatics analysis was conducted to characterize its physicochemical properties, protein structure, and phylogenetic relationship. RT-qPCR was used to analyze the expression pattern of GmECR14 under drought and salt stress. Subcellular localization was performed to determine the expression site of its encoded protein. Plant overexpression and knockout vectors were constructed, and the GmECR14 gene was introduced into soybean hairy roots and Arabidopsis thaliana via Agrobacterium-mediated genetic transformation to verify its function. Result The coding region of GmECR14 is 930 bp in length, encoding 309 amino acids, and the encoded protein was a typical transmembrane protein. Promoter analysis revealed that the presence of multiple cis-acting elements was related to abiotic stress in the gene promoter. Subcellular localization showed that the protein was localized in the endoplasmic reticulum. Phylogenetic analysis indicated that the soybean GmECR14 gene had a close genetic relationship with the AhECR protein sequence of peanut (Arachis hypogaea). Real-time fluorescent quantitative PCR analysis showed that the expression of GmECR14 was induced under both drought and salt stress. Phenotypic analysis, cuticular wax content determination, and stress tests (20% PEG 6000 and 200 mmol/L NaCl) of transgenic soybean hairy roots showed that: compared with the control, the overexpressing lines had significantly more lateral roots, the cuticular wax content was 0.24 times that of the control, and the tolerances to drought and salt were significantly improved. In contrast, the knockout lines had significantly fewer lateral roots, no difference in cuticular wax content compared with the control, and positive plants died after drought and salt stress. Heterologous expression of GmECR14 in A. thaliana showed that the cuticular wax content of overexpressing plants increased by 16.4% compared with the control, and the chlorophyll leaching rate and water loss rate of rosette leaves significantly decreased. Conclusion The GmECR14 gene positively regulates cuticular wax biosynthesis in soybeans and enhances the drought and salt tolerance of plants.

    Comparative Analysis of Floral Scent Formation between ‘Jinhui’ and Onc. ‘Sharry Baby’ of Oncidium hybridum
    FAN Rong-hui, LUO Yuan-hua, CHEN Yi-quan, FANG Neng-yan, CHEN Yan, ZHONG Huai-qin, YE Xiu-xian
    2026, 42(1):  105-113.  doi:10.13560/j.cnki.biotech.bull.1985.2025-0833
    Asbtract ( 118 )   HTML ( 1)   PDF (2635KB) ( 43 )  
    Figures and Tables | References | Related Articles | Metrics

    Objective A new strain ‘Jinhui’ was bred from tissue culture seedlings of Oncidium Gower Ramsey, which was tall and upright, but had no aroma. The aim of this study is to explore the non-aroma limiting factors of ‘Jinhui’ by analyzing molecular mechanism of floral scent formation involved in unscented ‘Jinhui’ and strong scented Onc. ‘Sharry Baby’, aiming to release aroma of ‘Jinhui’ by molecular technology. Method HS-SPME/GC-MS was used to determine components and contents of floral volatiles from two varieties of Oncidium hybridum. Key genes of floral scent formation were screened by transcriptome sequencing and qRT-PCR using different flower developmental stages of ‘Jinhui’ and Onc. ‘Sharry Baby’ as materials. Result GC-MS results showed that total floral volatile contents of blooming period in Onc. ‘Sharry Baby’ were 6.1 times higher than that of ‘Jinhui’. The main floral volatiles in Onc. ‘Sharry Baby’ was monoterpenes, while it was sesquiterpenes in ‘Jinhui’. The results of transcriptome sequencing showed that 55 277 unigenes were obtained, and about 81.64% unigenes were annotated by public database. In MEP pathway, the upstream pathway of monoterpenes, most of the genes, such as CMK, HDR, HDS and GPPS, were expressed higher in Onc. ‘Sharry Baby’ than that in ‘Jinhui’, thus that GPP, precursor of monoterpenes, was accumulated in the Onc. ‘Sharry Baby’. In MVA pathway, the upstream pathway of sesquiterpene, about half of genes were highly expressed in Onc. ‘Sharry Baby’, and half of them were highly expressed in ‘Jinhui’. Three terpene synthase genes (TPS) with significant differential expression were screened from transcriptome data. Among them, OhTPS1 and OhTPS2 belonged to the TPS-b family and were mainly composed of mono-TPSs genes. The expressions of OhTPS1 and OhTPS2 in Onc. ‘Sharry Baby’ were significantly higher than that in ‘Jinhui’ and increased gradually with flower development in Onc. ‘Sharry Baby’, indicating that these two genes played a key role in monoterpene biosynthesis of Onc. ‘Sharry Baby’. OhTPS3 belonged to TPS-a family and were mainly composed of sesqui-TPSs genes. The expression of OhTPS3 in ‘Jinhui’ was significantly higher than that in Onc. ‘Sharry Baby’ and increased gradually with flower development in ‘Jinhui’, indicating that this gene played a key role in sesquiterpenoid biosynthesis of ‘Jinhui’. Conclusion The main reason for low total amount of volatile compounds in ‘Jinhui’ flowers is that most of key genes in MEP pathway are low expression, which limits the accumulation of GPP, and low expression of monoterpene synthase genes also hinder the formation of monoterpene volatiles.

    Investigation into the Family Characteristics of the Lavender Copper Amine Oxidase Gene and the Role of LaCuAO1 in Bioamine Degradation
    HE Qi-chen, YANG Yang, ALIYA Waili, TANG Xin-yue, LI Zhong-xi, CHEN Yong-kun, CHEN Ling-na
    2026, 42(1):  114-124.  doi:10.13560/j.cnki.biotech.bull.1985.2025-0525
    Asbtract ( 893 )   HTML ( 1)   PDF (11182KB) ( 27 )  
    Figures and Tables | References | Related Articles | Metrics

    Objective This study aims to investigate the molecular characteristics of the CuAO gene family in lavender (Lavandula angustifolia) and the degradation function of LaCuAO1 in degrading bioamines, providing a reference for understanding the role of copper amine oxidase (CuAO) in plant metabolic regulation and biogenic amine degradation. Method Bioinformatics methods were used to identify the LaCuAO gene and screen from the genome data of lavender. The gene was cloned and then the recombinant Escherichia coli strains were constructed after optimizing the codons. High-performance liquid chromatography (HPLC) was to evaluate the degradation efficiency of ethanolamine and histamine. Result The 19 members of the LaCuAO family were identified from the lavender genome. The molecular weights of their encoded protein were of 39.8-87.4 kD, with 4-12 exons, and can be divided into 3 independent evolutionary branches. The analysis of gene expressions showed that the members of this family had significant tissue-specific expression characteristics. Among them, La15G00866 and La10G00763 showed constitutive high expression in multiple tissues such as roots, stems, and leaves, while La05G00442 was specifically and highly expressed only in flower buds and calyxes. The analysis of the promoter cis-acting elements showed that the promoter region was rich in light response elements and abscisic acid, low temperature, and other stress response elements. The engineered E. coli strain optLaCuAO1 (La05G00442) constructed through codon optimization has improved the degradation efficiency of ethanolamine and histamine from the wild type’s 50.0% and 92.1% to 62.5% and 93.2%, confirming its high efficiency in bioamine degradation. Conclusion The structural and expression characteristics of the LaCuAO gene family members in lavender are revealed, and the efficient degradation ability of the recombinant LaCuAO1 strain for ethanolamine and histamine is clarified. This provides a basis and reference for understanding the development mechanism of lavender and developing new methods for bioamine degradation.

    Identification of Sunflower GH3 Gene Family and Analysis of Their Function in Flower Development
    LONG Lin-xi, ZENG Yin-ping, WANG Qian, DENG Yu-ping, GE Min-qian, CHEN Yan-zhuo, LI Xin-juan, YANG Jun, ZOU Jian
    2026, 42(1):  125-138.  doi:10.13560/j.cnki.biotech.bull.1985.2025-0560
    Asbtract ( 118 )   HTML ( 2)   PDF (12544KB) ( 32 )  
    Figures and Tables | References | Related Articles | Metrics

    Objective Physicochemical property and expression feature of HaGH3 genes were analyzed to explore their functions in the floral development in sunflower (Helianthus annuus L.), and discover some molecular clues for sunflower breeding. Method Bioinformatics methods were adapted to identify the HaGH3 candidates based on the genome and transcriptome data of sunflower, and to analyze their physicochemical properties, chromosome localization, phylogenetic relationship, conserved motif, cis-acting elements, and tissue-expressing pattern. Subsequently, RT-qPCR was used to analyze the expression differences of HaGH3 genes between WT sunflower and cb1 (crazy broccoli 1) mutant in the phases of reproductive development (from St2 to St8), and to measure the expressions of HaGH3 genes in different flower organs of WT sunflower at St5 and St6 phases. Result The 19 members of HaGH3 gene family were in the sunflower genome, and named as HaGH3.1 to HaGH3.19, located on 12 chromosomes and categorized into two distinct subfamilies, and all members of the HaGH3 genes belonging to one subfamily possessed the same conserved domains. Transcription analysis indicated that 11 members presented the high expressions at the specific phase of flower development respectively, including HaGH3.1, HaGH3.2, HaGH3.3, HaGH3.4, HaGH3.5, HaGH3.8, HaGH3.11, HaGH3.12, HaGH3.13, HaGH3.14, and HaGH3.18. RT-qPCR analysis showed that the expressions of HaGH3.3, HaGH3.4, HaGH3.8, HaGH3.13, and HaGH3.14 reached their peak values in the St2 of WT, with significant differences between WT and cb1. HaGH3.1, HaGH3.2, HaGH3.5, HaGH3.12, and HaGH3.18 were highly expressed during St5 and St6 in WT, demonstrating obviously floral organs specificity. Cis-acting element analysis showed that a multitude of hormone response elements and MIKC_MADS recognition elements existed in the promoter regions of these 11 HaGH3 genes associated with floral development. Further analysis showed that HaGH3.8, HaGH3.14 and HaGH3.18 were regulated by ARF-mediated auxin signaling, HaGH3.1 and HaGH3.8 were regulated by gibberellin signal-related transcription factors such as MYB and bZIP, and HaGH3.2, HaGH3.8, HaGH3.13, HaGH3.14 and HaGH3.18 were regulated by the transcription factor MIKC_MADS. Conclusion Eleven members including HaGH3.1 and HaGH3.3 play important roles in regulating the growth and development of sunflower inflorescences. Among them, HaGH3.1, HaGH3.2, HaGH3.8, HaGH 3.13,HaGH 3.14 and HaGH 3.18 were regulated by auxin or gibberellin signal-related transcription factors and MADS-box members during flower development.

    Cloning and Functional Analysis of So4CL Gene in Syringa oblata
    NI Ying, LI Lei, WANG Jin-xuan, MA Bo, MENG Xin, LENG Ping-sheng, WU Jing, HU Zeng-hui
    2026, 42(1):  139-149.  doi:10.13560/j.cnki.biotech.bull.1985.2025-0557
    Asbtract ( 108 )   HTML ( 0)   PDF (4548KB) ( 19 )  
    Figures and Tables | References | Related Articles | Metrics

    Objective 4-coumarate∶CoA ligase (4CL) is a core enzyme of the phenylpropane metabolic pathway, and the function and expression characteristics of 4CL gene in Syringa oblata were investigated. Method Based on the genomic and transcriptomic data of S. oblata, the So4CL gene was screened and cloned. Bioinformatics analysis and subcellular localization were performed on its encoded protein. The relative expressions of So4CL in different flowering stages and tissues were investigated using RT-qPCR. The overexpressing and silencing vectors of So4CL were constructed and transformed into S. oblata and Nicotiana benthamian via Agrobacterium-mediated infection, followed by observation of phenotypic changes and measurement of anthocyanin content; and the expressions of the structural genes upstream and downstream of the anthocyanin biosynthesis pathway were determined by RT-qPCR. Result The CDS region of the So4CL gene was 1 659 bp in full length, encoding 552 amino acids with conserved structural domains BOXI and BOXII. Systematic evolutionary analysis revealed that So4CL had the highest 97% similarity to the 4CL protein of Fraxinus mandshurica. RT-qPCR analysis showed that the expression of the So4CL tended to decrease and then increase as the petals of lilac fading with flower development. So4CL was expressed in the roots, stems, leaves, and flowers in flowering stage. Subcellular localization analysis showed that So4CL was mainly present in the cytoplasm. The petals color of S. oblata got obviously darker after overexpressing So4CL, and the anthocyanin contents were significantly elevated. The N. benthamian leaves also showed brick-red changes. While petals were significantly discolored and anthocyanin contents significantly reduced after silencing So4CL. RT-qPCR analysis showed that transient transformation of So4CL affected the expressions of SoPAL, SoCHS, SoDFR, and SoUFGT in the anthocyanin biosynthesis pathway. Conclusion So4CL plays an important role in anthocyanin synthesis in S. oblata petals and is a key gene in this process.

    Cloning and Functional Analysis of AP2/ERF Transcription Factors RcERF4 and RcRAP2-12 in Rose
    YANG Juan, FENG Hui, JI Nai-zhe, SUN Li-ping, WANG Yun, ZHANG Jia-nan, ZHAO Shi-wei
    2026, 42(1):  150-160.  doi:10.13560/j.cnki.biotech.bull.1985.2025-0598
    Asbtract ( 130 )   HTML ( 1)   PDF (6530KB) ( 45 )  
    Figures and Tables | References | Related Articles | Metrics

    Objective The AP2/ERF transcription factor family plays crucial roles in regulating plant growth and development, flavonoid biosynthesis, and stress responses. Cloning the RcERF4 and RcRAP2-12 genes and analyzing their expression will lay the foundation for revealing the role of AP2/ERF transcription factors in regulating flower coloration in roses. Method First, RcERF4 and RcRAP2-12 were cloned from rose ‘Lady of Shalott’ via RT-PCR, followed by bioinformatic analysis, expression pattern profiling, and subcellular localization assays. Subsequently, positive transgenic tobacco plants overexpressing RcERF4 and RcRAP2-12 were generated via Agrobacterium-mediated leaf disk transformation, with transgenic phenotypes being systematically observed. Finally, the protein-protein interaction between RcERF4 and RcRAP2-12 was investigated through yeast two-hybrid (Y2H) and bimolecular fluorescence complementation (BiFC) assays. Result The open reading frame (ORF) of RcERF4 was 795 bp, encoding a protein of 264 amino acids, while the ORF of RcRAP2-12 was 1 179 bp, encoding a protein of 392 amino acids. Both RcERF4 and RcRAP2-12 proteins contained a single AP2 domain and belonged to the ERF subfamily. Phylogenetic analysis revealed a closer evolutionary relationship and higher protein homology with species such as Rosa rugosa and Fragaria vesca subsp. vesca. RcERF4 and RcRAP2-12 were primarily expressed in rose petals, stamens, and ovaries. RcERF4 had higher expressions during the early stages of flower development, while RcRAP2-12 showed an up-regulated expression trend throughout the entire petal coloring period. Subcellular localization demonstrated that both RcERF4 and RcRAP2-12 proteins localized to the nucleus. The overexpression of RcRAP2-12 in tobacco enhanced anthocyanin content in the corolla and upregulates the expression of NtANS, NtUFGT, and NtAN2. Furthermore, yeast two-hybrid (Y2H) and bimolecular fluorescence complementation (BiFC) assays confirmed that RcERF4 and RcRAP2-12 owned an interaction relationship. Conclusion RcERF4 and RcRAP2-12 are nuclear-localized ERF transcription factors, with RcRAP2-12 potentially playing a functional role in the formation and regulation of rose flower coloration.

    Cloning and Functional Analysis of ZhGSTF Related to Anthocyanin Transport Zantedeschia hybrida
    LYU Cheng-cong, HENG Meng, CHEN Si-qi, JIN Xue-hua
    2026, 42(1):  161-169.  doi:10.13560/j.cnki.biotech.bull.1985.2025-0747
    Asbtract ( 76 )   HTML ( 0)   PDF (2334KB) ( 23 )  
    Figures and Tables | References | Related Articles | Metrics

    Objective GSTF transporter is involved in the transport process of anthocyanins in plants. Studying its role and molecular mechanism in the coloration of spathe coloration and anthocyanin accumulation of Zantedeschia hybrida may provide theoretical basis for the analysis of anthocyanin transport mechanism of Z. hybrida and provide effective gene resources for breeding new varieties. Method Based on the analysis of transcriptome data of Z. hybrida, the gene ZhGSTF related to anthocyanin transport in the spatula of Z. hybrida was screened and cloned, its evolutionary relationship and sequence characteristics were analyzed, and the gene expressions and anthocyanin contents in different varieties of spatula were determined. Concurrently, virus induced gene silencing technology was used to construct ZhGSTF silencing system, and the variations of phenotype, gene expression and gene expression of three flavonoid synthesis pathways downstream after silencing were compared. Result The CDS of ZhGSTF gene was 666 bp long, encoding 221 amino acids. Phylogenetic tree analysis showed that ZhGSTF was clustered with GST related to anthocyanin transport in other species. The amino acid sequence comparison showed that ZhGSTF had the highest similarity with Perilla frutescens PFGST1. The expressions of ZhGSTF in rose ‘Lover’ and orange ‘Odean’ was significantly higher than that in yellow ‘Jincheng’, and it was significantly lower in white ‘Ventura’. The expressions of ZhGSTF in the four varieties were consistent with the accumulation trend of anthocyanins. After VIGS silencing, the expressions of ZhGSTF significantly decreased, and the phenotype of spathe faded obviously, but ZhGSTF silencing had no significant effect on the expression of ZhANS, ZhANR and ZhDFR. Conclusion The Z. hybridaZhGSTF promotes the accumulation of anthocyanins and affects its coloration in the process of spathe coloration.

    Starch Characterization and Related Gene Expression Analysis of Potato Germplasm Resources
    CHEN Jing-huan, FANG Guo-nan, ZHU Wen-hao, YE Guang-ji, SU Wang, HE Miao-miao, YANG Sheng-long, ZHOU Yun
    2026, 42(1):  170-183.  doi:10.13560/j.cnki.biotech.bull.1985.2025-1026
    Asbtract ( 64 )   HTML ( 0)   PDF (6610KB) ( 6 )  
    Figures and Tables | References | Related Articles | Metrics

    Objective To clarify the starch characteristics and differential gene expressions of potato ( Solanum tuberosum L.) germplasm resources provides superior genetic resources for variety improvement and breeding, laying a research foundation for elucidating the regulatory mechanisms of starch synthesis. Method Using 100 potato germplasm resources as materials, a comprehensive evaluation of starch content, amylose content, amylopectin content, amylopectin/amylose ratio, reducing sugars content and yield per plant was conducted through correlation analysis, principal component analysis, and cluster analysis. Result Correlation analysis indicated that amylose content was extremely negatively correlated with the amylopectin/amylose ratio and amylopectin content, while reducing sugars, starch content and yield per plant were significantly positively correlated. Principal component analysis identified three principal components: amylopectin content (ratio of amylopectin/amylose), reducing sugar content and starch content, with a cumulative contribution rate of 87.84%. Cluster analysis divided potato germplasm resources into three categories: Cluster I consisted of 32 samples, mainly characterized by late maturity and high starch content. Cluster II consisted of 40 samples, mainly characterized by early maturity and medium starch content. Cluster III consisted of 28 samples, mainly characterized by early maturity and low starch content. To elucidate the molecular mechanisms underlying starch content differences among potato varieties, the expressions of eight structural genes involved in the starch synthesis pathway (Susy4, AGPase, PTST1, etc.) were analyzed in high-starch varieties (Qingshu 2, Atlantic, 393034.7 and Shenyanwo) and low-starch varieties (FBA-1, Beishu 1, 2017ch-1 and 720018). The results showed that Susy4 and PTST1 expressions play a key role in determining starch content. Conclusion This study characterized the starch traits of 100 potato germplasm accessions and classified them into three groups, four high-starch potato varieties were selected (Qingshu 2, Atlantic, 393034.7 and Shenyanwo), confirming that the Susy4 and PTST1 genes are key regulators of starch content. These findings provide theoretical and material support for potato variety breeding and elucidating starch synthesis mechanisms.

    Genome-wide Identification of the BvATGs Genes Family in Sugar Beet (Beta vulgaris L.) and Analysis of Their Expression Pattern under Salt Stress
    REN Yun-er, WU Guo-qiang, CHENG Bin, WEI Ming
    2026, 42(1):  184-197.  doi:10.13560/j.cnki.biotech.bull.1985.2025-0504
    Asbtract ( 763 )   HTML ( 13)   PDF (14604KB) ( 39 )  
    Figures and Tables | References | Related Articles | Metrics

    Objective Autophagy is a crucial degradation pathway for maintaining cellular homeostasis and plays an essential role in plant responses to abiotic stress. In this study, autophagy-related genes (ATGs) were identified and characterized in sugar beet (Beta vulgaris L.), and their expression patterns under salt stress were analyzed to provide a theoretical basis for understanding their potential functions in stress responses. Method Members of the BvATGs gene family were identified from the sugar beet genome using bioinformatics methods, and the physicochemical properties, chromosomal distribution, phylogenetic relationships, gene structures, conserved motifs, cis-acting regulatory elements, and collinearity were analyzed. RT-qPCR was used to analyze the expression patterns of these genes under salt stress. The subcellular localization of BvATG4 and BvATG6a-1 was determined through transient transformation of Arabidopsisthaliana protoplasts mediated by PEG. Furthermore, the overexpression vectors for BvATG4 and BvATG6a-1 were constructed and genetically transformed into A.thaliana. Result A total of 51 BvATGs genes were identified and classified into 20 subfamilies in sugar beet. Among them, 48 BvATGs were unevenly distributed across nine chromosomes, while the other three genes (BvATG1a, BvATG1d and BvATG1k) were not mapped onto chromosomes. The BvATGs genes in the same subfamily had similar gene structures and conserved domains. The number of amino acids encoding BvATGs genes was 84-2 467 aa, and the molecular weight was 10.21-277.30 kD, most of which were hydrophilic proteins. Approximately 88.2% of the BvATGs members were localized to the cytoplasm, nucleus and chloroplast. Intraspecific collinearity analysis showed that there were 3 pairs of homologous genes of BvATGs, and interspecific collinearity showed that there were 9 pairs and 30 pairs of homologous genes of BvATGs in rice (Oryza sativa) and A. thaliana, respectively. A large number of light-responsive, hormone-responsive and stress-responsive elements were found in the promoter regions of the BvATGs genes. The RT-qPCR analysis showed that the expressions of 12 BvATG genes in the shoots and roots were up-regulated to varying degrees under salt stress. BvATG4 was primarily localized in the nucleus and cytoplasm, while BvATG6a-1 was mainly localized in the cytoplasm and endoplasmic reticulum. Compared to wild-type A. thaliana, the relative expressions of BvATG4 and BvATG6a-1 genes in the transgenic lines significantly increased. Conclusion A total of 51 BvATGs family members are identified at the whole genome of sugar beet in this study. Among those, 12 genes are differentially induced and up-regulated under salt stress. BvATG4 is localized in the nucleus and cytoplasm, while BvATG6a-1 is localized in the cytoplasm and endoplasmic reticulum. Further, BvATG4 and BvATG6a-1 are introduced into A. thaliana, and transgenic lines with high expression (OE4 and OE2) are obtained, respectively. This study establishs a theoretical basis for identification and utilization of salt-tolerant genetic resources in sugar beet.

    Bioinformatics Analysis of Peanut Transcription Factor AhHDZ70 and Its Tolerances to Salt and Drought
    WU Cui-cui, CHEN Deng-ke, LAN Gang, XIA Zhi, LI Peng-bo
    2026, 42(1):  198-207.  doi:10.13560/j.cnki.biotech.bull.1985.2025-0901
    Asbtract ( 641 )   HTML ( 15)   PDF (108005KB) ( 56 )  
    Figures and Tables | References | Related Articles | Metrics

    Objective Drought and salinity stress are critical environmental factors that severely affect the yield and quality of peanuts (Arachis hypogaea L.) in China. Investigating the structure and function of AhHDZ70 (Ah12g074600.1) gene will reveal its function in tolerance of peanut to drought and salt, and provide essential gene resources for peanut salt resistance and drought resistance breeding. Method Bioinformatics method were applied to analyze the physical and chemical properties, gene structure, phylogeny, cis-element of promoter, protein interaction of AhHDZ70. Fluorescence quantitative PCR technology was used to identify the expressions of AhHDZ70 gene in different tissues and organs, and under salt, drought, high temperature and low temperature stresses. Subcellular localization analysis was performed using tobacco transient transformation technology. Genetic transformation was carried out in Arabidopsis and biological function of AhHDZ70 was further verified by salt and drought stress treatment. Result AhHDZ70 encoded 326 amino acids, which was an unstable hydrophilic protein with no signal peptide, its secondary and tertiary structures were mainly characterized by irregular curling. Domain analysis showed that AhHDZ70 contained 4 exons and 3 introns. The AhHDZ70 promoter region contained two drought-induced functional elements (MBS motif), one adversity stress response element (TC-richrepeats motif), and one cryogenic response element (LTR motif). The main form of its secondary structure and tertiary structure was irregular curl. Transcriptome combined with RT-qPCR analysis showed that AhHDZ70 had the highest expression in seeds and responded positively to salt, drought, high temperature and low temperature stress. The results of subcellular localization showed that AhHDZ70 was located in the nucleus. AhHDZ70 heterologously overexpressed Arabidopsis to obtain homozygous transgenic plants. Under salt and drought stress, the germination rate of AhHDZ70-overexpressed transgenic lines was significantly higher than that of WT, and the root length was significantly longer than WT. Conclusion AhHDZ70 belongs to the HD-ZIP II transcription factor and is located in the nucleus. AhHDZ70 might play a regulatory role in the growth and development of various tissues in peanuts. Additionally, AhHDZ70 is likely involved in positively regulating peanut's response to salt and drought stress.

    Functional Analysis of the Transcription Factor MpR2R3-MYB17 in Regulating Gemma Development in Marchantia polymorpha L.
    ZENG Ting, ZHANG Lan, LUO Rui
    2026, 42(1):  208-217.  doi:10.13560/j.cnki.biotech.bull.1985.2025-0511
    Asbtract ( 76 )   HTML ( 3)   PDF (46994KB) ( 18 )  
    Figures and Tables | References | Related Articles | Metrics

    Objective To investigate the functional role and molecular mechanisms of the MpR2R3-MYB17 gene in regulating gemma development in Marchantia polymorpha L., providing novel insights into the regulatory network of gemma formation. Method Based on the reference genome information of M. polymorpha L., the full-length CDS sequence of MpR2R3-MYB17 was cloned. Bioinformatics analysis of its encoded protein was performed, and transient transformation in tobacco was conducted to detect the subcellular localization of MpR2R3-MYB17. The overexpression vector and CRISPR/Cas9 editing vector were constructed, and the transformed strains were obtained by Agrobacterium-mediated non-tissue culture-dependent transformation method to assess phenotypic changes. Result Bioinformatics analysis showed that the open reading frame of the MpR2R3-MYB17 was 1 277 bp, encoding 421 amino acids, had two conserved SANT domains, and was an R2R3-type MYB transcription factor. Phylogenetic analysis revealed that MpR2R3-MYB17 and the ninth subfamily of Arabidopsis R2R3-MYB converged into one branch, and the relationship with AtMYB17 was the closest. Subcellular localization analysis confirmed that the MpR2R3-MYB17 transcription factor was localized in the nucleus, suggesting its potential direct involvement in transcriptional regulation. The overexpression of MpR2R3-MYB17 caused a significant increase in gemma cup density and gemma number compared with wild or development of undifferentiated cell clumps (highly expressed) on the thallus of M. polymorpha L. The density of the gemma cup on the thallus and the number of the gemma in each gemma cup in the edited individual significantly reduced compared to the wild. Conclusion MpR2R3-MYB17, as a nuclear localization protein, is involved in regulating both gemma cup and gemma development.

    Genome-wide Identification of Panax notoginseng Lipoxygenases Coupled in Response to Methyl-jasmonate and Wounding
    LI Jian-bin, HOU Jia-e, LI Lei-lin, AI Ming-tao, LIU Tian-tai, CUI Xiu-ming, YANG Qian
    2026, 42(1):  218-229.  doi:10.13560/j.cnki.biotech.bull.1985.2025-0726
    Asbtract ( 107 )   HTML ( 2)   PDF (6022KB) ( 18 )  
    Figures and Tables | References | Related Articles | Metrics

    Objective To identify the Panax notoginsengLOX gene family and analyze its expression characteristics, thereby providing a basis for further investigation into the biological functions of the PnLOX genes. Method Bioinformatics methods were used to identify P. notoginseng LOX gene family and analyze its the phylogenetic relationship, gene structure characteristics, cis-elements and expression patterns of different plant tissues, MeJA treatment and wounding stress. Result Ten putative PnLOX genes were identified and formed three subgroups (9S-LOX, SG I 13S-LOX and SG II 13S-LOX ) according to phylogenetic tree and LOX substrate specificity. It was observed that LOX genes with similar evolutionary relationships had similar gene structures and conserved motifs. The PnLOX genes was located on six chromosomes and expanded mainly via segmental duplication (SD) and tandem duplication (TD). Subcellular localization prediction revealed that, except for PnLOX1/2/9 from SG I 13S-LOX subgroup, which localized to the chloroplast, all other PnLOX localized to the cytoplasm. Tissue expression analysis indicated that the PnLOX genes were differentially expressed in different tissues. The PnLOX1 and PnLOX2 genes were rapidly activated after MeJA treatment and wounding. Conclusion Ten putative PnLOX genes are identified from the P. notoginseng genome, among which the PnLOX1 and PnLOX2 genes may play an essential role in JA biosynthesis and JA-mediated damage repair in P. notoginseng.

    Study on the Function of Ata4CL Gene in Flavonoid Synthesis and Drought Resistance in Aster tataricus
    WANG Ting, MENG Yi-jiang, WANG Han, JIA Kai-xuan, QIAO Xiao-yu, HAN Bing-bing, LIU Xiao-qing, GE Shu-jun
    2026, 42(1):  230-240.  doi:10.13560/j.cnki.biotech.bull.1985.2025-0546
    Asbtract ( 99 )   HTML ( 1)   PDF (19360KB) ( 19 )  
    Figures and Tables | References | Related Articles | Metrics

    Objective As a cough-suppressing and lung-moistening medicinal herb, Aster tataricus L. contains flavonoid compounds as its main active components. 4-coumarate: CoA ligase (4CL) is the key rate-limiting enzyme for flavonoid synthesis. This study is aimed to explore the molecular characteristics of Ata4CL and its dual role in flavonoid synthesis and drought resistance, offering a theoretical basis for enhancing medicinal components of A. tataricus and breeding drought-resistant varieties. Method Total flavonoid content in different A. tataricus tissues and growth stages was measured by the aluminum nitrate colorimetric method. The full-length Ata4CL gene was cloned and its structural features analyzed using bioinformatics tools. Agrobacterium-mediated transformation was used for subcellular localization. A 35S::Ata4CL-6HA overexpression vector was constructed and transformed into Arabidopsis thaliana. Drought-stress experiments were carried out to verify its function. Result The total flavonoids in the roots of A. tataricus show a bimodal accumulation pattern, with the root being the main site for flavonoid accumulation. The highest flavonoid contents in the leaves and rhizomes are observed in plants entering the flowering stage. The full-length cDNA of the Ata4CL gene was cloned, which is 1 623 bp in length and encodes a protein of 540 amino acids with a molecular weight of 59.04 kD. The encoded protein is mainly composed of random coils, contains a conserved AAE domain, and is localized in chloroplasts. Its amino acid sequence is highly conserved among A. tataricus plants, with a homology of up to 96.48% with Conyza canadensis. The expressions of this gene in the roots and leaves both show an "increase-decrease-increase" trend, with the strongest expression in the roots of flowering plants and the highest expression in the flowers at the full flowering stage. The total flavonoid content in A. tataricus overexpressing Ata4CL is 1.47-1.76 times higher than that in wild-type plants, and the gene expression is up-regulated by 5.41-12.23 times. Meanwhile, the expressions of both upstream and downstream synthesis genes in the flavonoid pathway are up-regulated. Under drought stress, the survival rate of transgenic Arabidopsis is 76.67%-86.67% higher than that of wild-type plants, with significantly increased plant height, root length, and rosette diameter, enhanced SOD and POD activities, and decreased MDA content. Conclusion The Ata4CL gene enhances resistance in plants to drought by coordinately regulating flavonoid biosynthesis, thereby providing a key molecular target for the optimization of medicinal components in A. tataricus and the breeding of stress-resistant varieties.

    Cloning and Functional Analysis of a bZIP Transcription Factor MtbZIP29 from Medicago truncatula
    ZHANG Chi-hao, LIU Jin-nan, CHAO Yue-hui
    2026, 42(1):  241-250.  doi:10.13560/j.cnki.biotech.bull.1985.2025-0482
    Asbtract ( 165 )   HTML ( 9)   PDF (7911KB) ( 68 )  
    Figures and Tables | References | Related Articles | Metrics

    Objective Clone the MtbZIP29 gene from Medicago truncatula to study the self-activation, subcellular localization, and expression characteristics of the bZIP29 transcription factor, providing a theoretical research foundation for elucidating the involvement of the MtbZIP29 gene in the growth and development of M. truncatula and endogenous hormone signaling transduction. Method The MtbZIP29 gene was cloned from the wild-type M. truncatula 'R108', and expression vectors were constructed for experimental purposes. Subcellular localization was observed using a transient fusion protein assay, and using yeast to analyze its self-activation activity. Bioinformatics analyses were conducted on the MtbZIP29 gene, including protein physicochemical property analysis, prediction of promoter cis-acting elements, and prediction of secondary and tertiary protein structures. Additionally, RT-qPCR was employed to analyze the expression patterns of MtbZIP29 across different tissues and under treatments with various hormones (ABA, SA, 6-BA, IAA, and MeJA). Transgenic tobacco plants were obtained using Agrobacterium-mediated method, and the function of MtbZIP29 was analyzed. Result The MtbZIP29 gene was successfully cloned, with a coding sequence (CDS) length of 1,518 bp encoding 506 amino acids. The encoded protein had molecular weight of 55.830 kD, a theoretical isoelectric point (pI) of 6.82, an instability index of 63.60, and is classified as an unstable hydrophilic protein. Secondary structure prediction revealed that α-helixes accounted for 25.89%, extended strands for 0.59%, and the remaining 73.52% as random coils. Subcellular localization indicated the protein was localized to the nucleus. Yeast assays demonstrated the encoded protein has transcriptional self-activation activity. Expression profiling showed that MtbZIP29 transcripts were the most abundant in the leaves, significantly lower in the stems and pods compared to other tissues and markedly influenced by different hormone treatments. Analysis of MtbZIP29-overexpressing plants showed that the rhizomes of transgenic tobacco were significantly enlarged compared with wild-type tobacco. Conclusion The MtbZIP29 gene is involved in root growth and development, responding to different hormones, and may participate in the regulatory processes of root morphology construction and stress adaptability by integrating hormone signals.

    Identification and Expression Analysis of C2H2 Gene Family in Cenchrus purpureus
    YANG Dan, JIN Ya-rong, MAO Chun-li, WANG Bi-xian, ZHANG Ya-ning, YANG Zhi-yi, ZHOU Zhi-yao, YANG Rui-ming, FAN Heng-rui, HUANG Lin-kai, YAN Hai-dong
    2026, 42(1):  251-261.  doi:10.13560/j.cnki.biotech.bull.1985.2025-0902
    Asbtract ( 103 )   HTML ( 7)   PDF (3748KB) ( 28 )  
    Figures and Tables | References | Related Articles | Metrics

    Objective To identify C2H2-type zinc finger protein gene family members in Cenchrus purpureus (elephant grass) and explore their regulatory roles in cold stress responses, thereby laying a foundation for elucidating the functional mechanisms of C2H2 transcription factors. Method Based on the whole-genome data of elephant grass(Cenchrus purpureus), bioinformatics methods were used to systematically identify members of the C2H2 gene family. Transcriptome data and RT-qPCR were employed to analyze the expression patterns of these C2H2 genes under cold stress, and heterologous expression in Saccharomyces cerevisiae was performed to verify the functions of key genes. Result A total of 144 CpC2H2 genes were identified in C. purpureus. Phylogenetic analysis clustered these genes into 10 subgroups. Gene structure and conserved motif analyses revealed that members within the same subgroup exhibited highly conserved gene structures and conserved motifs. Cis-acting element analysis showed that 65 CpC2H2 genes contained cold-responsive cis-regulatory elements in their promoter regions. Expression pattern analysis indicated that the CpC2H2 gene family displayed distinct tissue-specific expression, among which CpC2H2-33, CpC2H2-107, CpC2H2-108, and CpC2H2-131 were significantly upregulated under cold stress. RT-qPCR results were consistent with transcriptome data. Heterologous expression experiments in S. cerevisiae confirmed that the encoded products of these four genes significantly enhanced the cold tolerance of recombinant strains. Conclusion A total of 144 C2H2 genes are identified in C. purpureus. The members of this family show distinct tissue specificity and differential expression under cold stress. Among them, CpC2H2-33, CpC2H2-107, CpC2H2-108, and CpC2H2-131 can enhance the cold tolerance of heterologous organisms, suggesting that they may play key roles in cold stress responses in C. purpureus. This study provides valuable insights for further investigating the functions of the C2H2 gene family and candidate genes for improving cold resistance in elephant grass through molecular breeding.

    Functional Analysis of Pg03852 Gene in Pyrenophora graminea
    MA Ru-qing, FENG Xue-qi, YANG Qing-lan, WANG Jun-cheng, MENG Ya-xiong, MA Xiao-le, LI Bao-chun, YAO Li-rong, WANG Hua-jun, SI Er-jing
    2026, 42(1):  262-270.  doi:10.13560/j.cnki.biotech.bull.1985.2025-0741
    Asbtract ( 94 )   HTML ( 4)   PDF (69923KB) ( 32 )  
    Figures and Tables | References | Related Articles | Metrics

    Objective To explore the function of gene Pg03852 in Pyrenophora graminea, thereby establishing a crucial theoretical foundation for studying the molecular interactions between this pathogen and its host plant. Method Based on transcriptomic data, the highly expressed gene Pg03852 during the host infection process of P. graminea was identified. Preliminary functional characterization of this gene was conducted by utilizing a combination of bioinformatic analyses, signal peptide activity assays, induction/suppression of immune responses, and the generation of RNA interference (RNAi) mutants followed by pathogenicity assessment. Result Bioinformatics analysis indicated that the Pg03852 gene encoded 276 amino acids, with a secondary structure predominantly composed of disordered coils accounting for 73.19%.Pg03852 was an unstable hydrophilic protein lacking transmembrane regions and conserved domains, but possessing a signal peptide and localized to the extracellular space. Signal peptide activity assays demonstrated that the Pg03852 signal peptide transformant grew normally on CMD-W and YPRAA media. TTC staining further confirmed the secretory function of this protein’s signal peptide. Results from immune response induction and inhibition experiments showed that Pg03852 did not induce cell necrosis but suppressed BAX-induced necrosis in plant tissues. Two RNAi mutants, Pg03852-RNAi-1 and Pg03852-RNAi-2, were obtained via PEG-mediated protoplast transformation. RT-qPCR results showed that Pg03852-RNAi-1 and Pg03852-RNAi-2 had expression reductions of 58.76% and 48.24% compared to the wild-type strain QWC, respectively, with disease incidence rates of 34.67% and 38.00% lower than the wild-type strain QWC. Both mutants also demonstrated significantly slower colony growth rates than the wild-type strain QWC (P<0.05). Histological observations revealed that hyphae in the RNAi mutants were denser, more convoluted, and had a slender morphology. Trypan blue staining and DAB staining results indicated that both the extent of cell death induced by infection with the interference mutants and the levels of reactive oxygen species accumulation were weaker than those observed in wild-type strain QWC. Conclusion Pg03852 is involved in the growth and development of the P. graminea and plays a critical role in regulating its pathogenicity.

    Construction of a Mild Vaccine of Zucchini Yellow Mosaic Virus and Its Cross-protective Efficacy
    ZHANG Yue, REN Qian, LUAN Ya-meng, LI Yi-chen, SUN Wu-xia, REN Shu-ying, XU Xiao-jie, SUN Xiao-hui
    2026, 42(1):  271-278.  doi:10.13560/j.cnki.biotech.bull.1985.2025-0944
    Asbtract ( 93 )   HTML ( 0)   PDF (2426KB) ( 38 )  
    Figures and Tables | References | Related Articles | Metrics

    Objective By investigating the effects of the mutation at the 364th conserved lysine (K364) in helper component-proteinase (HC-Pro) on the virulence of zucchini yellow mosaic virus (ZYMV), an attenuated ZYMV mutant were developed, and its genetic stability and cross-protection efficacy were assessed. Our study provided the theoretical basis for developing sustainable control strategies against ZYMV using attenuated strains. Method Using site-directed mutagenesis, the K364 residue in HC-Pro was substituted with aspartic acid (D) to investigate the effect of the K364D mutation on the virulence of ZYMV and the RNA silencing suppression activity of HC-Pro, thereby constructing the attenuated ZYMV-HC-ProK364D mutant. Furthermore, the genetic stability of ZYMV-HC-ProK364D mutant was assessed through serial passage of progeny viruses. The cross-protection efficacy of ZYMV-HC-ProK364D mutant was evaluated through cross-protection assays. Result The K364D mutation in HC-Pro attenuated ZYMV virulence, alleviated typical yellowing symptoms and reduced ZYMV accumulation in Cucumis melo plants. Simultaneously, K364D mutation suppressed the RNA silencing suppression activity of ZYMV HC-Pro. The attenuated mutant ZYMV-HC-ProK364D-GFP maintained genetic stability without reversion mutation after three successive passages in C. melo plants. In cross-protection assays, ZYMV-HC-ProK364D mutant induced significant resistance in C. melo plants against the wild-type ZYMV infection when the protection interval was 11 d. Conclusion The conserved K364 residue in HC-Pro was crucial in determining the RNA silencing suppression activity and the virulence of ZYMV. The ZYMV-HC-ProK436D mutant present excellent cross-protection efficacy and is a potential mild vaccine against the wild-type ZYMV infection in C. melo plants.

    Screening, Identification and Efficacy Determination of Biocontrol Bacteria against Pear Fire Blight
    ZHANG Man, DANG Jing-bo, JIANG Yuan, WEI Jie, XING Jie, WANG Zhe, SUN Li
    2026, 42(1):  279-293.  doi:10.13560/j.cnki.biotech.bull.1985.2025-0862
    Asbtract ( 111 )   HTML ( 7)   PDF (4040KB) ( 33 )  
    Figures and Tables | References | Related Articles | Metrics

    Objective Pear fire blight, caused by Erwinia amylovora, is a destructive bacterial disease causing a significant threat to pear and apple industries. This study aimed to screen strains with strong antagonistic activity against E. amylovora from the branches of Crataegus cuneata and Malus sieversii, providing microbial resources for the biological control of E. amylovora. Method The plate confrontation method was applied to screen the antagonistic strains against E. amylovora. The physiological and biochemical tests, 16S rDNA and rpoB gene sequencing were to determine the taxonomic status of these antagonistic strains. The methanol extractionwas to obtain in vitro antibacterial substances inhibiting E. amylovora. Thin-layer chromatography (TLC) was used to separate active components, and liquid chromatography-mass spectrometry (LC-MS) was used to identify the lipopeptide types in the fermentation broth. Bioinformatics analysis was conducted on the whole-genome data of KXI strain to explore its secondary metabolite gene clusters. The greenhouse control efficacy was tested on detached leaves, twigs, and young fruits of Korla fragrant pear (Pyrus sinkiangensis Yü). Result Seven strains with strong antagonistic activity against E. amylovora were isolated, among which KX1 showed the strongest antagonistic effect. Based on physiological and biochemical characteristics, 16S rDNA and rpoB gene sequence analysis, strain KX1 was identified as Bacillus velezensis. Preliminary detection revealed that the methanol extract of the B. velezensis KX1 contained lipopeptides, and TLC and LC-MS analysis revealed that surfactins were the major component of the lipopeptides. The crude lipopeptide extract retained antibacterial activity after treatments with different temperatures, pH values, storage times. The genome of strain KX1 was 4.1 Mb in size with a GC content of 46.33%. antiSMASH predicted that one secondary metabolite gene cluster shared 80% homology with the gene cluster related to fengycin. Greenhouse control efficacy tests showed that the disease index of immature Korla fragrant pear young fruits, leaves, and twigs in the protective experiment significantly reduced after inoculation with strain KX1. The disease prevention effects was 100%, 55.33%, and 70.65%, respectively, with protective efficacy being superior to therapeutic efficacy. Conclusion Bacillus velezensis KX1 effectively inhibit the activity of E. amylovora and has potential for biological control applications.

    Biological Characteristics and Genomic Analysis of a Novel Pathogen Strain Raoultella ornithinolytica Causing Soft Rot Disease in Konjac
    LIU Chang-ming, ZHANG Xin-yue, YANG Xin-meng, LIU Yang, LI Yue-han, WANG Ke-qing
    2026, 42(1):  294-304.  doi:10.13560/j.cnki.biotech.bull.1985.2024-1253
    Asbtract ( 97 )   HTML ( 2)   PDF (9409KB) ( 31 )  
    Figures and Tables | References | Related Articles | Metrics

    Objective The soft rot pathogen strain (Raoultella ornithinolytica Q-8, accession number: CP173279) was first isolated from the konjac (Amorphophallus spp.) corm. Sequence analysis and gene functional annotation were conducted at the whole-genome level, which will provide a theoretical basis for in-depth research on the pathogenic mechanisms of this strain and its effective control. Method Using third-generation whole-genome sequencing technology, genomic data were assembled and genes were predicted through software tools such as Canu, Prodigal, and RepeatMasker. Functional annotation and comparative analysis were performed using 12 databases, including KEGG and PHI-base. A phylogenetic tree was constructed based on the genomic ORF sequences using FastTree2. Result The genome size of Raoultella ornithinolytica Q-8 was 5.16 Mb with a GC content of 55.9%, including 4 962 coding DNA sequences (CDSs), 6 pseudogenes, 11 genomic islands, 25 rRNA genes, 129 other ncRNAs, and 16 different types of CRISPR systems. Among these, 4 833 genes were annotated into 22 gene clusters, and 3 126 genes were enriched in 114 metabolic pathways. Additionally, there were 1 714 transporter-related genes, 18 antibiotic resistance-related genes, 1 854 pathogen-host interaction-related genes, and 1 067 virulence factor-related genes. Phylogenetic tree analysis revealed that R. ornithinolytica Q-8 and other 8 strains of R. ornithinolytica wore clustered in the same large branch while distantly related to two previously reported pathogens of konjac soft rot, P. carotovorum and D. chrysanthemi. Conclusion R. ornithinolytica Q-8 is a novel pathogenic agent causing konjac soft rot. Its genome harbors multiple antibiotic resistance genes and pathogen-host interaction genes, which are likely to play crucial roles in its virulence mechanisms.

    Isolation and Identification of a Heterotrophic Nitrifying Bacterium from the Compost of Chinese Medicinal Herbal Residues and Study of Its Nitrification and Denitrification Capabilities
    ZHENG Wan-ting, ZENG Qian-nuo, FU Jia-yi, RAO Min-xin, HE Guo-zhen, ZHANG Ying
    2026, 42(1):  305-314.  doi:10.13560/j.cnki.biotech.bull.1985.2024-1049
    Asbtract ( 79 )   HTML ( 0)   PDF (1888KB) ( 26 )  
    Figures and Tables | References | Related Articles | Metrics

    Objective To achieve efficient nitrogen retention during the aerobic composting of Chinese medicinal herbal residues (CMHRs), this study is aimed to isolate and identify microorganisms with high nitrification capacity and to elucidate their nitrification-denitrification characteristics, thereby providing potential microbial resources and a theoretical basis for developing nitrogen-conserving microbial agents. Method Pure strains were obtained from CMHRs compost using the enrichment culture, spread plate, and streak plate methods. Screening based on heterotrophic nitrification capability led to the selection of the high-efficiency strain. Identification of the strain was performed based on morphological characteristics and 16S rDNA gene sequencing. The effects of environmental factors on strain growth and nitrification capacity were investigated by adjusting six cultivation conditions: carbon source, carbon to nitrogen ratio (C/N), initial ammonium nitrogen concentration, pH, temperature, and rotational speed. The denitrification capability of strain YF-5 was examined by culturing it in media with nitrite nitrogen or nitrate nitrogen as the sole nitrogen source. Result A highly efficient nitrifying bacterium was isolated from the compost and named YF-5, which was identified as Alcaligenes aquatilis by morphological observation and molecular biology. Optimization experiments determined that the optimal nitrification conditions for this strain included a carbon source of sodium succinate, a C/N of 20, an initial ammonium nitrogen concentration of 100 mg/L, a pH of 7.0, a temperature of 35 ℃, and a rotation speed of 160 r/min. Analysis of nitrified products indicated that strain YF-5 performed heterotrophic nitrification with the accumulation of nitrite nitrogen. Denitrification experiments confirmed that strain YF-5 was incapable of employing nitrite or nitrate nitrogen as substrates for denitrification. Conclusion Strain YF-5 converts ammonium nitrogen into stable nitrite nitrogen under optimized conditions and lacks denitrification capability. This characteristic enables it to reduce both ammonia volatilization and denitrification through targeted nitrogen conversion during CMHRs composting, thereby minimizing nitrogen loss and demonstrating promising application potential.

    Screening, Identification and Biological Activity of Three Sulfur-oxidizing Bacteria
    CHEN Yan, LIU Xin, SHI Zhu-feng, PU Te, LIU En-de, ZHANG Yi-jie, CAO Yan-ru, YANG Pei-wen
    2026, 42(1):  315-328.  doi:10.13560/j.cnki.biotech.bull.1985.2025-0731
    Asbtract ( 69 )   HTML ( 2)   PDF (27920KB) ( 15 )  
    Figures and Tables | References | Related Articles | Metrics

    Objective To address the issues of low sulfur availability in agricultural soils and sulfur deficiency in crops, this study is aimed to screen sulfur-oxidizing bacteria (SOB) with both high sulfur oxidation efficiency and multiple bioactivities from the rhizosphere soil of oilseed rape in Yunnan, China, and to evaluate their potential for agricultural application. Method SOB were isolated using targeted enrichment and isolation techniques. Sulfur oxidation activity was evaluated based on pH reduction and sulfate production. Isolates were screened for multifunctional PGP traits, including nitrogen fixation, zinc solubilization, and phosphate solubilization. Promising strains were further assessed for biological activities such as siderophore production, heteroauxin (IAA) secretion, and antagonism against plant pathogens. Their efficacy in promoting seed germination and Solanum lycopersicum plant growth was validated. Result A total of 313 SOB strains were isolated. Among them, 16 Strains presented strong sulfur-oxidizing capacity (sulfate production: 38.53-66.54 mg/L). Based on morphological, physiological, biochemical characteristics, and 16S rDNA sequence analysis, three high-activity strains, YNK-FB0053, YNK-FB0056, and YNK-FB0057, were identified as Burkholderia gladioli, Pantoea endophytica, and Priestia aryabhattai, respectively. All three strains possessed the activities of nitrogen fixation, zinc solubilization, phosphate solubilization, and siderophore secretion. They also harbored genes associated with antibiotic synthesis (srfAB, yndJ, ituC, sboA, bioA, NRPS, and PKSI). Seed germination tests demonstrated that these strains increased germination rates of Brassica napus L, Solanum lycopersicum, and Secale cereale by 16.67%–44.33% and total seedling length by 17.95%–33.70%. In pot experiments with Solanum lycopersicum, all three strains significantly (P<0.05) promoted plant growth, with chlorophyll content, plant height, and stem diameter increased by approximately 15%–30%, root length extended by more than 55%, and belowground biomass showing the most pronounced improvement. In terms of nutrient accumulation, total nitrogen, phosphorus, potassium, and sulfur contents were all enhanced, while iron content had the greatest increase, reaching 112.50%. Conclusion The rhizosphere soil of Yunnan oilseed rape harbors SOB strains with both high-efficiency sulfur oxidation and multiple plant growth-promoting functions. Strain YNK-FB0053 (B. gladioli), YNK-FB0056 (P. endophytica), and YNK-FB0057 (P. aryabhattai) significantly enhance seed germination, Solanum lycopersicum plant growth, and mineral element accumulation, demonstrating substantial potential for agricultural application as novel multifunctional bioinoculants.

    Overexpression of the xylR Gene Driven by Different Promoters Enhances Glucose-xylose Co-utilization Capability in Escherichia coli
    LI Zheng, QIU Wei-yue, SUN Rui-xue, ZHAO Xiao
    2026, 42(1):  329-337.  doi:10.13560/j.cnki.biotech.bull.1985.2025-0794
    Asbtract ( 371 )   HTML ( 1)   PDF (3700KB) ( 31 )  
    Figures and Tables | References | Related Articles | Metrics

    Objective To mitigate the Carbon Catabolite Repression (CCR) effect and enhance the co-utilization capacity of glucose and xylose by Escherichia coli (E. coli). Method Using the D-lactic acid-producing engineered E. coli strain JH15 as the starting strain, the xylR gene encoding the xylose regulatory factor was overexpressed via the pBR322 plasmid carrying four different promoters (PcysG, PrrsA, PJ23119, and PpflBp6). Four recombinant strains, namely CX-A15, RX-A15, JX-A15, and PX-A15, were constructed. Quantitative real-time polymerase chain reaction (qPCR) analysis and fermentation experiments were further performed to compare the transcription levels of xylose transport and metabolism genes, as well as changes in fermentation performance, among all strains under the carbon source condition of 30 g/L glucose + 20 g/L xylose. Result After xylR overexpresed, the transcription levels of key xylose metabolism genes (xylA and xylB) and xylose transport-related genes (xylF, xylG, and xylH) increased in all recombinant strains. Compared with the parent strain JH15: 1) The xylose consumption rates of CX-A15, RX-A15, JX-A15, and PX-A15 increased by 22%, 84%, 206%, and 209%, respectively; 2) the D-lactic acid production rates increased by 8%, 27%, 97%, and 98%, respectively. Among the recombinant strains, JX-A15 and PX-A15 completely consumed the carbon source within 48 h and achieved the maximum D-lactic acid yield. Their fermentation cycle was shortened by 43% compared with the 84-h cycle of JH15. Conclusion The overexpression of the xylR gene driven by promoters PJ23119 and PpflBp6 can effectively reduce the CCR effect. While ensuring D-lactic acid yield, this strategy significantly improves the co-utilization of glucose and xylose by the D-lactic acid-producing engineered bacteria, enhances production intensity, and shortens the fermentation cycle. It provides technical support for promoting industrial fermentation using low-cost raw materials such as lignocellulose.

    Inotodiol Prevention of Aflatoxin B1-induced Liver Injury by Activating Nrf2/PGC-/Mitophagy
    KANG Kai, YANG Wei, LI Ying-chun, XIE Wei-tian, WU Hai-yan, YOU Yu-pin, CHEN Zhi-bao
    2026, 42(1):  338-351.  doi:10.13560/j.cnki.biotech.bull.1985.2025-0600
    Asbtract ( 60 )   HTML ( 2)   PDF (56116KB) ( 10 )  
    Figures and Tables | References | Related Articles | Metrics

    Objective Inotodiol (INO), a triterpenoid compound extracted from the fungus Phaeoporus obliquus, a dual-purpose fungus for both medicine and food. It possesses biological activities such as antioxidant and anti-inflammatory properties. The protective effect of INO on the hepatotoxicity of aflatoxin B1 (AFB1) was studied through in vivo and in vitro experiments. Method The mouse liver and Alpha mouse liver 12 cell (AML12) injury model were established using AFB1. Liver tissue sections were prepared to analyze the pathological changes. The antioxidant levels in liver tissues, serum and AML12 cells were analyzed through ELISA and antioxidant-related detection kits. Reactive oxygen species (ROS) and mitochondrial membrane potential (MMP) were detected by fluorescence microscopy. The expressions of Nrf2, PGC-1α, and mitophagy signaling pathway proteins in liver and AML12 cells were detected by Western blot and qPCR. Result AFB1 significantly increased the activities of CYP450, AST, and ALT in the liver and AML12 cells (P<0.01). Pretreatment with INO significantly reduced these proteins’ expressions (P<0.01). INO significantly reversed (P<0.01) the decline in antioxidant capacity and mitochondrial dysfunction induced by AFB1. Analysis of Nrf2, PGC-1α and mitophagy signaling pathways revealed that INO significantly alleviated AFB1-induced suppression of these pathways, and ultimately attenuated oxidative damage and restoring mitochondrial dysfunction caused by AFB1. Conclusion INO inhibits AFB1-induced hepatotoxicity both in vitro and in vivo. The protective effect of INO on the liver is closely related to the activation of the Nrf2/PGC-1α signaling pathway and the promotion of mitophagy.

    Content
    2026, 42(1):  352. 
    Asbtract ( 14 )   PDF (1261KB) ( 15 )  
    Related Articles | Metrics
    copyright
    2026, 42(1):  353. 
    Asbtract ( 16 )   PDF (155KB) ( 4 )  
    Related Articles | Metrics
    Cover
    2026, 42(1):  354. 
    Asbtract ( 10 )   PDF (97626KB) ( 5 )  
    Related Articles | Metrics