Conserved Composition of Nod Factors and Exopolysaccharides Produced by Different Phylogenetic Lineage Sinorhizobium Strains Nodulating Soybean
文献类型: 外文期刊
作者: Wang, Dan 2 ; Couderc, Francois 2 ; Tian, Chang Fu 3 ; Gu, Wenjie 1 ; Liu, Li Xue 3 ; Poinsot, Verena 2 ;
作者机构: 1.Guangdong Acad Agr Sci, Inst Agr Resources & Environm, Key Lab Plant Nutr & Fertilizer South Reg, Minist Agr,Guangdong Key Lab Nutrient Cycling & F, Guangzhou, Guangdong, Peoples R China
2.UMR5623 Univ Paul Sabatier, CNRS, Lab IMRCR, Toulouse, France
3.China Agr Univ, State Key Lab Agrobiotechnol, Beijing, Peoples R China
4.China Agr Univ, Coll Biol Sci, Beijing, Peoples R China
关键词: exopolysaccharide; mass spectrometry; Nod factors; Sinorhizobium; soybean
期刊名称:FRONTIERS IN MICROBIOLOGY ( 影响因子:5.64; 五年影响因子:6.32 )
ISSN: 1664-302X
年卷期: 2018 年 9 卷
页码:
收录情况: SCI
摘要: The structural variation of symbiotic signals released by rhizobia determines the specificity of their interaction with legume plants. Previous studies showed that Sinorhizobium strains from different phylogenetic lineages had different symbiotic performance on certain cultivated soybeans. Whether they released similar or different symbiotic signals remained unclear. In this study, we compared their nod and exo gene clusters and made a detailed structural analysis of Nod factors and EPS by ESI-MS/MS and two dimensions NMR. Even if there are some differences among nod or exo gene clusters; they produced much conserved Nod factor and EPS compositions. The Nod factors consist of a cocktail of beta-(1, 4)-linked tri-, tetra-, and pentamers of N-acetyl-D-glucosamine (GlGNAc). The C2 position on the non-reducing terminal end is modified by a lipid chain that contains 16 or 18 atoms of carbon-with or without unsaturations-, and the C6 position on the reducing residue is decorated by a fucose or a 2-O-methylfucose. Their EPS are composed of glucose, galactose, glucuronic acid, pyruvic acid in the ratios 5:1:2:1 or 6:1:2:1. These findings indicate that soybean cultivar compatibility of Sinorhizobium strains does not result from Nod factor or EPS structure variations. The structure comparison of the soybean microbionts with other Sinorhizobium strains showed that Nod factor structures of soybean microbionts are much conserved, although there are no specific genes shared by the soybean microsymbionts. EPS produced by Sinorhizobium strains are different from those of Bradyrhizobium. All above is consistent with the previous deduction that Nod factor structures are related to host range, while those of EPS are connected with phylogeny.
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