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集胞藻6803(Synechocystis sp. strain PCC6803)中羧酶体形成所需的一个基因(ccmA)。

A gene (ccmA) required for carboxysome formation in the cyanobacterium Synechocystis sp. strain PCC6803.

作者信息

Ogawa T, Marco E, Orus M I

机构信息

Solar Energy Research Group, Institute of Physical and Chemical Research (Riken), Saitama, Japan.

出版信息

J Bacteriol. 1994 Apr;176(8):2374-8. doi: 10.1128/jb.176.8.2374-2378.1994.

Abstract

A high-CO2-requiring mutant, G7, of Synechocystis sp. strain PCC6803 capable of inorganic carbon transport but unable to utilize the intracellular inorganic carbon pool for photosynthesis was isolated. Transmission electron micrographs of the mutant indicated that the mutant does not have any carboxysomes. A clone (pHPG7) with a 7.5-kbp DNA insert that transforms the G7 mutant to the wild-type phenotype was isolated from a genomic library of wild-type Synechocystis sp. strain PCC6803. Complementation tests with subclones identified the mutation site in G7 within 208 bp. Sequencing of nucleotides in this region elucidated an open reading frame, designated ccmA, encoding a protein of 302 amino acids. Cloning and sequence analysis of the respective G7 gene revealed an A-to-G substitution that results in an Asp-to-Gly substitution in the deduced amino acid. The result indicated that the ccmA gene encodes a protein essential for the formation of carboxysomes. An open reading frame encoding a proline-rich protein of 271 amino acids was found downstream of the ccmA gene, but no ccm-like genes or rbc operon was found in this region.

摘要

分离出了集胞藻PCC6803菌株的一个高二氧化碳需求突变体G7,它能够进行无机碳转运,但无法利用细胞内无机碳库进行光合作用。该突变体的透射电子显微镜图像显示,该突变体没有任何羧酶体。从野生型集胞藻PCC6803菌株的基因组文库中分离出一个带有7.5千碱基对DNA插入片段的克隆(pHPG7),该克隆可将G7突变体转化为野生型表型。用亚克隆进行的互补试验确定了G7中208碱基对范围内的突变位点。对该区域核苷酸的测序揭示了一个开放阅读框,命名为ccmA,编码一个302个氨基酸的蛋白质。对相应G7基因的克隆和序列分析揭示了一个A到G的替换,导致推导氨基酸中一个天冬氨酸到甘氨酸的替换。结果表明,ccmA基因编码一种对羧酶体形成至关重要的蛋白质。在ccmA基因下游发现了一个编码271个氨基酸的富含脯氨酸蛋白质的开放阅读框,但在该区域未发现ccm样基因或rbc操纵子。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5063/205361/3f882160d4cd/jbacter00026-0252-a.jpg

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