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黄色粘球菌的rfbABC操纵子编码一种O抗原生物合成和多细胞发育所需的ATP结合盒转运蛋白同源物。

The Myxococcus xanthus rfbABC operon encodes an ATP-binding cassette transporter homolog required for O-antigen biosynthesis and multicellular development.

作者信息

Guo D, Bowden M G, Pershad R, Kaplan H B

机构信息

Department of Microbiology and Molecular Genetics, University of Texas Medical School, Houston 77030, USA.

出版信息

J Bacteriol. 1996 Mar;178(6):1631-9. doi: 10.1128/jb.178.6.1631-1639.1996.

Abstract

A wild-type sasA locus is critical for Myxococcus xanthus multicellular development. Mutations in the sasA locus cause defective fruiting body formation, reduce sporulation, and restore developmental expression of the early A-signal-dependent gene 4521 in the absence of A signal. The wild-type sasA locus has been located on a 14-kb cloned fragment of the M. xanthus chromosome. The nucleotide sequence of a 7-kb region containing the complete sasA locus was determined. Three open reading frames encoded by the genes, designated rfbA, B and C were identified. The deduced amino acid sequences of rfbA and rfbB show identity to the integral membrane domains and ATPase domains, respectively, of the ATP-binding cassette (ABC) transporter family. The highest identities are to a set of predicted ABC transporters required for the biosynthesis of lipopolysaccharide O-antigen in certain gram-negative bacteria. The rfbC gene encodes a predicted protein of 1,276 amino acids. This predicted protein contains a region of 358 amino acids that is 33.8% identical to the Yersinia enterocolitica O3 rfbH gene product, which is also required for O-antigen biosynthesis. Immunoblot analysis revealed that the sasA1 mutant, which was found to encode a nonsense codon in the beginning of rfbA, produced less O-antigen than sasA+ strains. These data indicate that the sasA locus is required for the biosynthesis of O-antigen and, when mutated, results in A-signal-independent expression of 4521.

摘要

野生型sasA基因座对黄色黏球菌的多细胞发育至关重要。sasA基因座的突变会导致子实体形成缺陷、孢子形成减少,并在没有A信号的情况下恢复早期A信号依赖性基因4521的发育表达。野生型sasA基因座已定位在黄色黏球菌染色体的一个14 kb克隆片段上。测定了包含完整sasA基因座的一个7 kb区域的核苷酸序列。鉴定出由这些基因编码的三个开放阅读框,分别命名为rfbA、B和C。rfbA和rfbB推导的氨基酸序列分别与ATP结合盒(ABC)转运蛋白家族的整合膜结构域和ATP酶结构域具有同一性。最高的同一性是与某些革兰氏阴性菌中脂多糖O抗原生物合成所需的一组预测ABC转运蛋白。rfbC基因编码一个预测的1276个氨基酸的蛋白质。这个预测的蛋白质包含一个358个氨基酸的区域,与小肠结肠炎耶尔森氏菌O3 rfbH基因产物有33.8%的同一性,该基因产物也是O抗原生物合成所必需的。免疫印迹分析显示,在rfbA起始处编码无义密码子的sasA1突变体产生的O抗原比sasA+菌株少。这些数据表明,sasA基因座是O抗原生物合成所必需 的,并且在发生突变时会导致4521的A信号非依赖性表达。

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