首页> 外文OA文献 >Induction of the gap-pgk operon encoding glyceraldehyde-3-phosphate dehydrogenase and 3-phosphoglycerate kinase of Xanthobacter flavus requires the LysR-type transcriptional activator CbbR.
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Induction of the gap-pgk operon encoding glyceraldehyde-3-phosphate dehydrogenase and 3-phosphoglycerate kinase of Xanthobacter flavus requires the LysR-type transcriptional activator CbbR.

机译:诱导黄嘌呤杆菌编码3-磷酸甘油醛脱氢酶和3-磷酸甘油酸激酶的gap-pgk操纵子需要LysR型转录激活因子CbbR。

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摘要

In a previous study, a gene (pgk) encoding phosphoglycerate kinase was isolated from a genomic library of Xanthobacter flavus. Although this gene is essential for autotrophic growth, it is not located within the cbb operon encoding other Calvin cycle enzymes. An analysis of the nucleotide sequence upstream from pgk showed the presence of a gene encoding glyceraldehyde-3-phosphate dehydrogenase and the 3' end of an open reading frame encoding a protein which is 50% identical to transketolase encoded by cbbT of X. flavus. Gene fusions between pgk and lacZ demonstrated that the gap and pgk genes are organized in an operon. Induction of the Calvin cycle in heterotrophically growing cells resulted in a sixfold increase in phosphoglycerate kinase activity in parallel with the appearance of ribulosebisphosphate carboxylase activity. This superinduction of phosphoglycerate kinase did not occur in an X. flavus strain in which cbbR, encoding the transcriptional activator of the cbb operon, was disrupted. The failure to superinduce the gap-pgk operon is not caused by the absence of a functional Calvin cycle, since the expression of this operon in an X. flavus strain with a defective ribulosebisphosphate carboxylase enzyme was the same as the expression in the wild type. It is therefore concluded that the expression of both the cbb and gap-pgk operons is controlled by CbbR.
机译:在先前的研究中,从黄杆菌的基因组文库中分离出编码磷酸甘油酸激酶的基因(pgk)。尽管该基因对于自养生长至关重要,但它并不位于编码其他卡尔文循环酶的cbb操纵子内。对pgk上游核苷酸序列的分析表明,存在编码甘油醛-3-磷酸脱氢酶的基因,以及一个开放阅读框的3'端,该开放阅读框编码的蛋白质与黄曲霉的cbbT编码的转酮醇酶具有50%的同一性。 pgk和lacZ之间的基因融合表明,gap和pgk基因在操纵子中组织。在异养生长的细胞中卡尔文循环的诱导导致磷酸甘油酸酯激酶活性增加了六倍,同时出现了核糖二磷酸羧化酶活性。磷酸甘油酸激酶的这种超诱导作用在黄曲霉菌株中没有发生,在黄曲霉菌株中,编码cbb操纵子转录激活因子的cbbR被破坏。无法产生gap-pgk操纵子不是由于没有功能性的卡尔文循环引起的,因为该操纵子在具有缺陷的核糖二磷酸羧化酶的黄萎病菌中的表达与野生型中的表达相同。因此得出结论,cbb和gap-pgk操纵子的表达均受CbbR控制。

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