首页> 外文期刊>Molecular Plant-Microbe Interactions >Host-dependent expression of Rhizobium leguminosarum bv. viciae hydrogenase is controlled at transcriptional and post-transcriptional levels in legume nodules.
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Host-dependent expression of Rhizobium leguminosarum bv. viciae hydrogenase is controlled at transcriptional and post-transcriptional levels in legume nodules.

机译:豆根瘤菌bv的宿主依赖性表达。蚕豆中的蚕豆氢化酶控制在转录水平和转录后水平。

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摘要

The legume host affects the expression of Rhizobium leguminosarum hydrogenase activity in root nodules. High levels of symbiotic hydrogenase activity were detected in R. leguminosarum bacteroids from different hosts, with the exception of lentil (Lens culinaris). Transcription analysis showed that the NifA-regulated R. leguminosarum hydrogenase structural gene promoter (P(1)) is poorly induced in lentil root nodules. Replacement of the P(1) promoter by the FnrN-dependent promoter of the fixN gene restored transcription of hup genes in lentil bacteroids, but not hydrogenase activity. In the P(fixN)-hupSL strain, additional copies of the hup gene cluster and nickel supplementation to lentil plants increased bacteroid hydrogenase activity. However, the level of activity in lentil still was significantly lower than in pea bacteroids, indicating that an additional factor is impairing hydrogenase expression inside lentil nodules. Immunological analysis revealed that lentil bacteroids contain reduced levels of both hydrogenase structural subunit HupL and nickel-binding protein HypB. Altogether, results indicate that hydrogenase expression is affected by the legume host at the level of both transcription of hydrogenase structural genes and biosynthesis or stability of nickel-related proteins HypB and HupL, and suggest the existence of a plant-dependent mechanism that affects hydrogenase activity during the symbiosis by limiting nickel availability to the bacteroid.
机译:豆类宿主影响根瘤中豆根瘤菌氢化酶活性的表达。除小扁豆外,在不同宿主的豆科豆球菌细菌中检测到高水平的共生氢化酶活性。转录分析表明,在扁豆根瘤中,NifA调控的豆科念珠菌氢化酶结构基因启动子(P(1))的诱导较弱。 FixN基因的FnrN依赖性启动子替换P(1)启动子恢复了扁豆类细菌中hup基因的转录,但没有氢化酶活性。在P(fixN)-hupSL菌株中,hup基因簇的其他拷贝和对扁豆植物的镍补充增加了类细菌氢化酶的活性。然而,小扁豆中的活性水平仍然显着低于豌豆类细菌,这表明另一个因素正在损害小扁豆结节内的氢化酶表达。免疫学分析表明,扁豆类细菌的氢化酶结构亚基HupL和镍结合蛋白HypB含量均降低。总之,结果表明,豆科植物宿主在氢化酶结构基因的转录以及镍相关蛋白HypB和HupL的生物合成或稳定性方面都影响了氢化酶的表达,并表明存在影响氢化酶活性的植物依赖性机制。在共生过程中,通过限制镍对类细菌的利用率。

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