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光合电子传递通过对glnB基因产物的翻译后修饰来控制蓝藻中的氮同化。

Photosynthetic electron transport controls nitrogen assimilation in cyanobacteria by means of posttranslational modification of the glnB gene product.

作者信息

Tsinoremas N F, Castets A M, Harrison M A, Allen J F, Tandeau de Marsac N

机构信息

Département de Biochimie et Génétique Moléculaire, Institut Pasteur, Paris, France.

出版信息

Proc Natl Acad Sci U S A. 1991 Jun 1;88(11):4565-9. doi: 10.1073/pnas.88.11.4565.

Abstract

A glnB gene is identified in the cyanobacterium Synechococcus sp. PCC 7942, and its gene product is found to be covalently modified as a result of imbalance in electron transfer in photosynthesis, where photosystem II is favored over photosystem I. The gene was cloned and sequenced and found to encode a polypeptide of 112 amino acid residues, whose sequence shows a high degree of similarity to the Escherichia coli regulatory protein, PII. In E. coli, PII is involved in signal transduction in transcriptional and post-translational regulation of nitrogen assimilation. Increase in ammonium ion concentration is shown to decrease covalent modification of the Synechococcus PII protein, as in enteric bacteria. We therefore propose that the photosynthetic electron transport chain may regulate the pathway of nitrogen assimilation in cyanobacteria by means of posttranslational, covalent modification of the glnB gene product. The existence of the glnB gene in different strains of cyanobacteria is demonstrated and its implications are discussed.

摘要

在蓝藻聚球藻属(Synechococcus sp.)PCC 7942中鉴定出了glnB基因,并且发现其基因产物由于光合作用中电子传递失衡而发生共价修饰,其中光系统II比光系统I更受青睐。该基因被克隆并测序,发现它编码一个由112个氨基酸残基组成的多肽,其序列与大肠杆菌调节蛋白PII具有高度相似性。在大肠杆菌中,PII参与氮同化转录和翻译后调节中的信号转导。如在肠道细菌中一样,铵离子浓度的增加会降低聚球藻PII蛋白的共价修饰。因此,我们提出光合电子传递链可能通过对glnB基因产物进行翻译后共价修饰来调节蓝藻中的氮同化途径。证明了glnB基因在不同蓝藻菌株中的存在并讨论了其意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2ecc/51705/812f440691a3/pnas01061-0014-a.jpg

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