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首页> 外文期刊>Journal of bacteriology >The Myxococcus xanthus rfbABC operon encodes an ATP-binding cassette transporter homolog required for O-antigen biosynthesis and multicellular development.
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The Myxococcus xanthus rfbABC operon encodes an ATP-binding cassette transporter homolog required for O-antigen biosynthesis and multicellular development.

机译:黄腐粘球菌rfbABC操纵子编码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。

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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.
机译:野生型sasA基因座对于黄色粘球菌多细胞发育至关重要。 sasA基因座中的突变会导致子实体形成缺陷,减少孢子形成,并在缺乏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基因座已位于X.xanthus染色体的14 kb克隆片段上。确定了包含完整sasA基因座的7-kb区域的核苷酸序列。鉴定了由基因编码的三个开放阅读框,命名为rfbA,B和C。推导的rfbA和rfbB的氨基酸序列分别显示出与ATP结合盒(ABC)转运蛋白家族的完整膜结构域和ATPase结构域的同一性。最高的身份是在某些革兰氏阴性细菌中生物合成脂多糖O抗原所需的一组预测的ABC转运蛋白。 rfbC基因编码1276个氨基酸的预测蛋白。该预测的蛋白质包含358个氨基酸的区域,与小肠结肠炎耶尔森菌O3 rfbH基因产物具有33.8%的同一性,这也是O抗原生物合成所必需的。免疫印迹分析表明,发现sasA1突变体在rfbA开头编码无义密码子,其产生的O抗原少于sasA +菌株。这些数据表明,sasA基因座是O抗原生物合成所必需的,并且在突变时会导致不依赖A信号的4521表达。

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