Reshetnikov Alexander S, Khmelenina Valentina N, Trotsenko Yuri A
G.K. Skryabin Institute of Biochemistry and Physiology of Microorganisms, Russian Academy of Sciences, Pushchino, 142290 Moscow region, Russia.
Arch Microbiol. 2006 Jan;184(5):286-97. doi: 10.1007/s00203-005-0042-z. Epub 2005 Nov 10.
The genes involved in biosynthesis of the major compatible solute ectoine (1,4,5,6-tetrahydro-2-methylpyrimidine carboxylic acid) in halotolerant obligate methanotroph "Methylomicrobium alcaliphilum 20Z" were studied. The complete nucleotide sequences of the structural genes encoding L: -aspartokinase (Ask), L-2,4-diaminobutyric acid transaminase (EctB), L-2,4-diaminobutyric acid acetyltransferase (EctA), and L-ectoine synthase (EctC) were defined and shown to be transcribed as a single operon ectABCask. Phylogenetic analysis revealed high sequence identities (34-63%) of the Ect proteins to those from halophilic heterotrophs with the highest amino acid identities being to Vibrio cholerae enzymes. The chromosomal DNA fragment from "M. alcaliphilum 20Z" containing ectABC genes and putative promoter region was expressed in Escherichia coli. Recombinant cells could grow in the presence of 4% NaCl and synthesize ectoine. The data obtained suggested that despite the ectoine biosynthesis pathway being evolutionary well conserved with respect to the genes and enzymes involved, some differences in their organization and regulation could occur in various halophilic bacteria.
对嗜盐专性甲烷氧化菌“嗜碱甲基微菌20Z”中参与主要相容性溶质四氢嘧啶(1,4,5,6 - 四氢 - 2 - 甲基嘧啶羧酸)生物合成的基因进行了研究。确定了编码L - 天冬氨酸激酶(Ask)、L - 2,4 - 二氨基丁酸转氨酶(EctB)、L - 2,4 - 二氨基丁酸乙酰转移酶(EctA)和L - 四氢嘧啶合酶(EctC)的结构基因的完整核苷酸序列,并表明它们作为一个单一的操纵子ectABCask进行转录。系统发育分析显示,Ect蛋白与嗜盐异养菌的Ect蛋白具有较高的序列同一性(34 - 63%),其中与霍乱弧菌酶的氨基酸同一性最高。含有ectABC基因和假定启动子区域的“嗜碱甲基微菌20Z”染色体DNA片段在大肠杆菌中表达。重组细胞能够在4% NaCl存在的情况下生长并合成四氢嘧啶。获得的数据表明,尽管四氢嘧啶生物合成途径在涉及的基因和酶方面在进化上高度保守,但在各种嗜盐细菌中它们的组织和调控可能存在一些差异。