[1] Chistoserdova L, Vorholt JA, Thauer RK, et al.C1 transfer enzymes and coenzymes linking methylotrophic bacteria and methanogenic Archaea[J]. Science, 1998, 281:99-102. [2] Lee MC, Chou HH, Marx CJ.Asymmetric, bimodal trade-offs during adaptation of Methylobacterium to distinct growth substrates[J]. Evolution, 2009, 63:2816-2830. [3] Chou HH, Chiu HC, Delaney NF, et al.Diminishing returns epistasis among beneficial mutations decelerates adaptation[J]. Science, 2011, 332:1190-1192. [4] Vu HN, Subuyuj GA, Vijayakumar S, et al.Lanthanide-Dependent Regulation of Methanol Oxidation Systems in Methylobacterium extorquens AM1 and Their Contribution to Methanol Growth[J]. J Bacteriol, 2016, 198:1250-1259. [5] Marx CJ, Lidstrom ME.Development of improved versatile broad-host-range vectors for use in methylotrophs and other Gram-negative bacteria[J]. Microbiology, 2001, 147:2065-2075. [6] Chubiz LM, Purswani J, Carroll SM, et al.A novel pair of inducible expression vectors for use in Methylobacterium extorquens[J]. BMC Res Notes, 2013, 6:183. [7] Matz MV, et al.Fluorescent proteins from nonbiolumi-nescent Anthozoa species[J]. Nat Biotechnol, 1999, 17:969-973. [8] Shaner NC, Campbell RE, et al.Improved monomeric red, orange and yellow fluorescent proteins derived from Discosoma sp. red fluorescent protein[J]. Nat Biotechnol, 2004, 22:1567-1572. [9] Shu X, Royant A, Lin MZ, et al.Mammalian expression of infrared fluorescent proteins engineered from a bacterial phytochrome[J]. Science, 2009, 324:804-807. [10] Day RN, Davidson MW.The fluorescent protein palette:tools for cellular imaging[J]. Chem Soc Rev, 2009, 38:2887-2921. [11] Michener JK, et al.Phylogeny poorly predicts the utility of a challenging horizontally transferred gene in Methylobacterium strains[J]. J Bacteriol, 2014, 196:2101-2107. [12] Figueira MM, Laramee L, et al.Production of green fluorescent protein by the methylotrophic bacterium methylobacterium extorquens[J]. FEMS Microbiol Lett, 2000, 193:195-200. [13] Marx CJ, Lidstrom ME.Development of an insertional expression vector system for Methylobacterium extorquens AM1 and generation of null mutants lacking mtdA and/or fch[J]. Microbiology, 2004, 150:9-19. [14] Sy A, Timmers AC, Knief C, et al.Methylotrophic metabolism is advantageous for Methylobacterium extorquens during colonization of Medicago truncatula under competitive conditions[J]. Appl Environ Microbiol, 2005, 71:7245-7252. [15] Liang WF, Sun MY, Cui LY, et al.Cre/loxP-Mediated Multicopy Integration of the Mevalonate Operon into the Genome of Methylobacterium extorquens AM1[J]. Appl Biochem Biotechnol, 2018, 185:565-577. [16] Choi YJ, Morel L, Bourque D, et al.Bestowing inducibility on the cloned methanol dehydrogenase promoter(PmxaF)of Methylobacterium extorquens by applying regulatory elements of Pseudomonas putida F1[J]. Appl Environ Microbiol, 2006, 72:7723-7729. [17] Guiziou S, Sauveplane V, Chang HJ, et al.A part toolbox to tune genetic expression in Bacillus subtilis[J]. Nucleic Acids Res, 2016, 44:7495-7508. [18] Singh A, Azad M, Shymko MD, et al.The BH3 only Bcl-2 family member BNIP3 regulates cellular proliferation[J]. PLoS One, 2018, 13:e0204792. [19] Yang YM, Chen WJ, Yang J, et al.Production of 3-hydroxypropionic acid in engineered Methylobacterium extorquens AM1 and its reassimilation through a reductive route[J]. Microb Cell Fact, 2017, 16:179. [20] Heim R, Cubitt AB, Tsien RY.Improved green fluorescence[J]. Nat, 1995, 373:663-664. |