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酒类酒球菌合成胞外多糖:从基因到表型

Exopolysaccharide (EPS) synthesis by Oenococcus oeni: from genes to phenotypes.

作者信息

Dimopoulou Maria, Vuillemin Marlène, Campbell-Sills Hugo, Lucas Patrick M, Ballestra Patricia, Miot-Sertier Cécile, Favier Marion, Coulon Joana, Moine Virginie, Doco Thierry, Roques Maryline, Williams Pascale, Petrel Melina, Gontier Etienne, Moulis Claire, Remaud-Simeon Magali, Dols-Lafargue Marguerite

机构信息

Université de Bordeaux, Institut polytechnique de Bordeaux, ISVV, EA 4577, Unité de recherche Oenologie, INRA USC 1366, Villenave d'Ornon, France.

Université de Toulouse, INSA, UPS, INP, INRA, CNRS, LISBP, Toulouse, France.

出版信息

PLoS One. 2014 Jun 5;9(6):e98898. doi: 10.1371/journal.pone.0098898. eCollection 2014.

DOI:10.1371/journal.pone.0098898
PMID:24901216
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4047060/
Abstract

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.

摘要

酒酒球菌是驱动葡萄酒中苹果酸-乳酸发酵的细菌物种。对50个酒酒球菌基因组序列(14个已有的和36个新测序的)进行分析,列出了可能参与胞外多糖(EPS)生物合成的基因清单。鉴定出的基因座有:两个名为eps1和eps2的基因簇,三个分离的糖苷水解酶基因dsrO、dsrV和levO,以及三个分离的糖基转移酶基因gtf、it3、it4。这些分离的基因根据菌株的不同而存在或缺失,并且eps基因簇的组成因菌株而异。在不同培养基中生长后,检测了几种菌株的可溶性和荚膜EPS生产能力,并确定了EPS的结构。基因型与表型的相关性表明,酒酒球菌中有几种EPS生物合成途径是活跃且互补的。可以区分出:(i)一种依赖Wzy的合成途径,主要以荚膜形式产生由葡萄糖、半乳糖和鼠李糖组成的杂多糖;(ii)一种葡聚糖合酶途径(Gtf),以游离和细胞相关形式参与β-葡聚糖的合成,使生长培养基呈现粘稠表型;(iii)由GH70和GH68家族的糖苷水解酶从蔗糖合成同多糖(α-葡聚糖或β-果聚糖)。研究了eps基因在系统发育树上的分布。50个研究基因组中有50个拥有几个专门用于EPS代谢的基因。这表明这些聚合物对于酒酒球菌适应其特定的生态位——葡萄酒很重要,并且可能有助于苹果酸-乳酸发酵起始剂的技术性能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8743/4047060/4b8a4d7f50d1/pone.0098898.g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8743/4047060/0445ce25b175/pone.0098898.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8743/4047060/5f5301375ae8/pone.0098898.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8743/4047060/073ea801fec3/pone.0098898.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8743/4047060/ba7abef7e742/pone.0098898.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8743/4047060/72e634b7dd68/pone.0098898.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8743/4047060/e22db21b6651/pone.0098898.g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8743/4047060/4b8a4d7f50d1/pone.0098898.g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8743/4047060/0445ce25b175/pone.0098898.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8743/4047060/5f5301375ae8/pone.0098898.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8743/4047060/073ea801fec3/pone.0098898.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8743/4047060/ba7abef7e742/pone.0098898.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8743/4047060/72e634b7dd68/pone.0098898.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8743/4047060/e22db21b6651/pone.0098898.g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8743/4047060/4b8a4d7f50d1/pone.0098898.g007.jpg

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