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Molecular and mutational analysis of a DNA region separating two methylotrophy gene clusters in Methylobacterium extorquens AM1

机译:将两种甲基杆菌基因簇分离甲基杆菌溶剂AM1的分子和突变分析

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A region of 14-2 kb has been analysed that is a part of a locus on the Methylobacterium extorquens AM1 chromosome containing a number of genes involved in one-carbon (C1) metabolism, including serine cycle genes, pqq genes, regulatory methanol oxidation genes and the gene for N5,N10-methylene tetrahydrofolate dehydrogenase (mtdA). Fifteen new ORFs have been identified within the new region, and their sequences suggest that they encode the following polypeptides: the C-terminal part of phosphoenolpyruvate carboxylase, malyl-CoA lyase, polypeptides of 9.4 and 31 kDa of unknown function, three putative subunits of an ABC-type transporter, two polypeptides similar to the products of mxaF and mxaJ from M. extorquens AM1 and other methylotrophs, a cytochrome c, three enzymes of folate metabolism, and polypeptides of 13 and 20.5 kDa with no homologues in the protein database. Ten insertion mutations have been generated in the region to determine if the newly identified genes are associated with C1 metabolism. A mutation in mcIA. encoding malyl-CoA lyase, resulted in a C1-minus phenotype, while mutations in the other genes all showed a C1-plus phenotype. It was not possible to obtain null mutants in a putative folate metabolism gene, foIC, implying the necessity of these folate synthesis genes for metabolism of C1 and multicarbon compounds. Mutations in the putative ABC transporter genes, the genes similar to mxaG and mxaJ, and other unidentified ORFs produced double-crossover recombinants with a C1-positive phenotype. Promoter regions have been investigated upstream of orf3 and orf4 using the promoter probe vector pHX200. Transcription from these promoters was weak in wild-type M. extorquens AM1 but increased in regulatory mox mutants.
机译:已经分析了14-2 kB的区域,即甲基杆菌溶剂上的基因座的一部分含有涉及单碳(C1)代谢的许多基因,包括丝氨酸循环基因,PQQ基因,调节甲醇氧化基因和N5,N10-亚甲基四氢脱液脱氢酶(MTDA)的基因。已经在新地区鉴定了十五个新ORF,它们的序列表明它们编码以下多肽:磷酸丙酮酸羧酸盐羧化酶的C末端部分,丙基-CoA裂解酶,9.4和31kDa的未知功能,三个推定亚基ABC型转运蛋白,两种多肽类似于MXAF和MXAJ的产物,来自M. intercorquens AM1和其他甲基萎缩,一种细胞色素C,叶酸代谢的三种酶,13和20.5kDa的多肽,蛋白质数据库没有同源物。在该区域中产生了十个插入突变,以确定新鉴定的基因是否与C1代谢相关。麦利亚的突变。编码丙基-COA裂解酶,导致C1-minus表型,而其他基因中的突变均显示出C1-Plus表型。在推定的叶酸代谢基因,FOIC中无法获得零突变体,暗示这些叶酸合成基因的必要性,用于C1和多元金属化合物的代谢。推定ABC转运蛋白基因中的突变,类似于MXAG和MXAJ的基因,以及其他未识别的ORF产生双交叉重组剂,具有C1阳性表型。使用启动子探针载体pHX200在ORF3和ORF4的上游研究了启动子区域。来自这些启动子的转录在野生型M.幽默AM1中弱,但在调节MOX突变体中增加。

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