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由cccA编码的枯草芽孢杆菌13千道尔顿细胞色素c-550由一个膜锚定结构域和一个血红素结构域组成。

Bacillus subtilis 13-kilodalton cytochrome c-550 encoded by cccA consists of a membrane-anchor and a heme domain.

作者信息

von Wachenfeldt C, Hederstedt L

机构信息

Department of Microbiology, Univsrsity of Lund, Sweden.

出版信息

J Biol Chem. 1990 Aug 15;265(23):13939-48.

PMID:2166045
Abstract

Little is known about c-type cytochromes in Gram-positive bacteria in contrast to the wealth of information available on this type of cytochrome in Gram-negative bacteria and in eucaryotes. In the present work, the strictly aerobic bacterium Bacillus subtilis was analyzed for subcellular localization and number of different cytochromes c. In vivo labeling with radioactive 5-aminolevulinic acid, a precursor to heme, showed that the proteins containing covalently bound heme are predominantly found in the membrane fraction. One major membrane-bound cytochrome c of about 15 kDa and with an alpha-band absorption peak in the reduced state at 550 nm was analyzed in more detail. Cytochrome c-550 has the properties of an integral membrane protein. The physiological function of this relatively high redox potential cytochrome is not known. Its structural gene, cccA, was cloned, sequenced, and overexpressed in B. subtilis. The gene maps adjacent to rpoD (sigA) at 223 degrees on the chromosome. The amino acid sequence of cytochrome c-550 as deduced from the DNA sequence consists of 120 residues and contains one heme c binding site (Cys-Ile-Ala-Cys-His) located approximately in the middle of the polypeptide. From the hydropathy distribution and from comparisons to soluble c-type cytochromes of known three-dimensional structure, cytochrome c-550 seemingly consists of two domains; an N-terminal membrane-anchor domain and a C-terminal heme domain. A model for the topography of the cytochrome in the cytoplasmic membrane is suggested in which the N-terminal part spans the membrane in the form of a single segment in an alpha-helical conformation and the C-terminal heme domain is exposed on the extracytoplasmic side of the membrane. Deletion of cccA from the chromosome revealed another membrane-bound cytochrome with absorption maximum at 550 nm in the reduced state. Analysis of cccA deletion mutants demonstrated that the cytochrome c-550 encoded by cccA is not essential for growth of B. subtilis on rich or minimal media.

摘要

与革兰氏阴性菌和真核生物中有关此类细胞色素的丰富信息相比,人们对革兰氏阳性菌中的c型细胞色素了解甚少。在本研究中,对严格需氧菌枯草芽孢杆菌进行了分析,以确定不同细胞色素c的亚细胞定位和数量。用放射性5-氨基乙酰丙酸(一种血红素前体)进行体内标记表明,含有共价结合血红素的蛋白质主要存在于膜组分中。对一种约15 kDa、还原态α带吸收峰在550 nm的主要膜结合细胞色素c进行了更详细的分析。细胞色素c-550具有整合膜蛋白的特性。这种相对高氧化还原电位的细胞色素的生理功能尚不清楚。其结构基因cccA被克隆、测序并在枯草芽孢杆菌中过表达。该基因位于染色体上223°处,与rpoD(sigA)相邻。从DNA序列推导的细胞色素c-550的氨基酸序列由120个残基组成,包含一个血红素c结合位点(Cys-Ile-Ala-Cys-His),大约位于多肽的中间位置。从亲水性分布以及与已知三维结构的可溶性c型细胞色素的比较来看,细胞色素c-550似乎由两个结构域组成;一个N端膜锚定结构域和一个C端血红素结构域。提出了细胞质膜中细胞色素拓扑结构的模型,其中N端部分以α螺旋构象的单个片段形式跨越膜,C端血红素结构域暴露在膜的胞外一侧。从染色体上缺失cccA后,发现了另一种在还原态时吸收最大值在550 nm的膜结合细胞色素。对cccA缺失突变体的分析表明,由cccA编码的细胞色素c-550对于枯草芽孢杆菌在丰富或基本培养基上的生长不是必需的。

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