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Identification and Molecular Characterization of the Chromosomal Exopolysaccharide Biosynthesis Gene Cluster from Lactococcus lactis subsp. cremoris SMQ-461

机译:乳酸乳球菌亚种的染色体胞外多糖生物合成基因簇的鉴定和分子表征。 creemoris SMQ-461

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摘要

The exopolysaccharide (EPS) capsule-forming strain SMQ-461 of Lactococcus lactis subsp. cremoris, isolated from raw milk, produces EPS with an apparent molecular mass of >1.6 × 106 Da. The EPS biosynthetic genes are located on the chromosome in a 13.2-kb region consisting of 15 open reading frames. This region is flanked by three IS1077-related tnp genes (L. lactis) at the 5′ end and orfY, along with an IS981-related tnp gene, at the 3′ end. The eps genes are organized in specific regions involved in regulation, chain length determination, biosynthesis of the repeat unit, polymerization, and export. Three (epsGIK) of the six predicted glycosyltransferase gene products showed low amino acid similarity with known glycosyltransferases. The structure of the repeat unit could thus be different from those known to date for Lactococcus. Reverse transcription-PCR analysis revealed that the eps locus is transcribed as a single mRNA. The function of the eps gene cluster was confirmed by disrupting the priming glycosyltransferase gene (epsD) in Lactococcus cremoris SMQ-461, generating non-EPS-producing reversible mutants. This is the first report of a chromosomal location for EPS genetic elements in Lactococcus cremoris, with novel glycosyltransferases not encountered before in lactic acid bacteria.
机译:乳酸乳球菌亚种的胞外多糖(EPS)胶囊形成菌株SMQ-461。从生乳中分离出的鸡腿草产生的EPS的表观分子量> 1.6×106 Da。 EPS生物合成基因位于染色体上的13.2kb区域中,该区域由15个开放阅读框组成。该区域的两侧为5'端和orfY的三个IS1077相关tnp基因(乳酸乳球菌),以及3'端为IS981相关的tnp基因。 eps基因组织在特定区域,涉及调节,链长确定,重复单元的生物合成,聚合和输出。六个预测的糖基转移酶基因产物中的三个(epsGIK)与已知糖基转移酶的氨基酸相似性较低。因此,重复单元的结构可以与迄今为止已知的乳球菌不同。逆转录-PCR分析显示,eps基因座被转录为单个mRNA。通过破坏cremoriscus cremoris SMQ-461中的启动糖基转移酶基因(epsD),产生了不产生EPS的可逆突变体,证实了eps基因簇的功能。这是关于Cremoococcus cremoris中EPS遗传元件的染色体位置的首次报道,在乳酸菌中以前没有遇到过新的糖基转移酶。

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    Dabour, N.; LaPointe, G.;

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  • 年度 2005
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