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茎瘤固氮根瘤菌胞外多糖的结构表征及其对喙毛萼田菁根瘤起始的重要性。

Structural characterization of extracellular polysaccharides of Azorhizobium caulinodans and importance for nodule initiation on Sesbania rostrata.

作者信息

D'Haeze Wim, Glushka John, De Rycke Riet, Holsters Marcelle, Carlson Russell W

机构信息

Complex Carbohydrate Research Center, The University of Georgia, 315 Riverbend Road, Athens, GA 30602-4712, USA.

出版信息

Mol Microbiol. 2004 Apr;52(2):485-500. doi: 10.1111/j.1365-2958.2004.03989.x.

Abstract

During lateral root base nodulation, the microsymbiont Azorhizobium caulinodans enters its host plant, Sesbania rostrata, via the formation of outer cortical infection pockets, a process that is characterized by a massive production of H(2)O(2). Infection threads guide bacteria from infection pockets towards nodule primordia. Previously, two mutants were constructed that produce lipopolysaccharides (LPSs) similar to one another but different from the wild-type LPS, and that are affected in extracellular polysaccharide (EPS) production. Mutant ORS571-X15 was blocked at the infection pocket stage and unable to produce EPS. The other mutant, ORS571-oac2, was impaired in the release from infection threads and was surrounded by a thin layer of EPS in comparison to the wild-type strain that produced massive amounts of EPS. Structural characterization revealed that EPS purified from cultured and nodule bacteria was a linear homopolysaccharide of alpha-1,3-linked 4,6-O-(1-carboxyethylidene)-D-galactosyl residues. In situ H(2)O(2) localization demonstrated that increased EPS production during early stages of invasion prevented the incorporation of H(2)O(2) inside the bacteria, suggesting a role for EPS in protecting the microsymbiont against H(2)O(2). In addition, ex planta assays confirmed a positive correlation between increased EPS production and enhanced protection against H(2)O(2).

摘要

在侧根基部结瘤过程中,微共生体茎瘤固氮根瘤菌通过形成外皮层感染袋进入其宿主植物喙荚田菁,这一过程的特征是大量产生H₂O₂。感染丝将细菌从感染袋导向根瘤原基。此前构建了两个突变体,它们产生的脂多糖(LPS)彼此相似,但与野生型LPS不同,且在胞外多糖(EPS)产生方面受到影响。突变体ORS571-X15在感染袋阶段受阻,无法产生EPS。另一个突变体ORS571-oac2在从感染丝中释放方面受损,与产生大量EPS的野生型菌株相比,其被一层薄薄的EPS包围。结构表征显示,从培养细菌和根瘤细菌中纯化的EPS是由α-1,3-连接的4,6-O-(1-羧基亚乙基)-D-半乳糖基残基组成的线性同多糖。原位H₂O₂定位表明,入侵早期EPS产量增加可阻止H₂O₂进入细菌内部,这表明EPS在保护微共生体免受H₂O₂侵害方面发挥作用。此外,离体实验证实EPS产量增加与对H₂O₂的保护增强之间存在正相关。

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