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Exopolysaccharide (EPS) Synthesis by Oenococcus oeni: From Genes to Phenotypes

机译:Oenococcus oeni的胞外多糖(EPS)合成:从基因到表型。

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摘要

Oenococcus oeni is the bacterial species which drives malolactic fermentation in wine. The analysis of 50 genomic sequences of O. oeni (14 already available and 36 newly sequenced ones) provided an inventory of the genes potentially involved in exopolysaccharide (EPS) biosynthesis. The loci identified are: two gene clusters named eps1 and eps2, three isolated glycoside-hydrolase genes named dsrO, dsrV and levO, and three isolated glycosyltransferase genes named gtf, it3, it4. The isolated genes were present or absent depending on the strain and the eps gene clusters composition diverged from one strain to another. The soluble and capsular EPS production capacity of several strains was examined after growth in different culture media and the EPS structure was determined. Genotype to phenotype correlations showed that several EPS biosynthetic pathways were active and complementary in O. oeni. Can be distinguished: (i) a Wzy -dependent synthetic pathway, allowing the production of heteropolysaccharides made of glucose, galactose and rhamnose, mainly in a capsular form, (ii) a glucan synthase pathway (Gtf), involved in β-glucan synthesis in a free and a cell-associated form, giving a ropy phenotype to growth media and (iii) homopolysaccharide synthesis from sucrose (α-glucan or β-fructan) by glycoside-hydrolases of the GH70 and GH68 families. The eps gene distribution on the phylogenetic tree was examined. Fifty out of 50 studied genomes possessed several genes dedicated to EPS metabolism. This suggests that these polymers are important for the adaptation of O. oeni to its specific ecological niche, wine and possibly contribute to the technological performance of malolactic starters.
机译:Oenococcus oeni是导致葡萄酒中苹果酸乳酸发酵的细菌。 O. oeni的50个基因组序列的分析(已有14个新序列和36个新测序的序列)提供了可能与胞外多糖(EPS)生物合成相关的基因的清单。确定的基因座是:两个名为eps1和eps2的基因簇,三个分离的名为dsrO,dsrV和levO的糖苷水解酶基因,以及三个分离的名为gtf,it3,it4的糖基转移酶基因。根据菌株的不同,是否存在分离的基因,eps基因簇的组成从一种菌株转移到另一种菌株。在不同培养基中生长后,检查了几种菌株的可溶性和荚膜EPS生产能力,并确定了EPS结构。基因型与表型的相关性表明O. oeni中的几种EPS生物合成途径是活跃的和互补的。可以区分:(i)Wzy依赖性合成途径,允许生产主要以荚膜形式由葡萄糖,半乳糖和鼠李糖制成的杂多糖,(ii)参与β-葡聚糖合成的葡聚糖合酶途径(Gtf)。以游离和与细胞相关的形式存在,使生长培养基呈露比表型,并且(iii)通过GH70和GH68家族的糖苷水解酶从蔗糖(α-葡聚糖或β-果聚糖)合成同多糖。检查了系统发育树上的eps基因分布。在研究的50个基因组中,有50个具有几个专门用于EPS代谢的基因。这表明这些聚合物对于O. oeni适应其特定生态位,葡萄酒非常重要,并且可能对苹果酸发酵剂的技术性能有所贡献。

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