Regulation of Rhizobial Nodulation Genes by Flavonoid-Independent NodD Supports Nitrogen-Fixing Symbioses With Legumes

IF 4.3 2区 生物学 Q2 MICROBIOLOGY
Timothy L. Haskett, Louise Cooke, Patrick Green, Philip S. Poole
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Abstract

Rhizobia and legumes form a symbiotic relationship resulting in the formation of root structures known as nodules, where bacteria fix nitrogen. Legumes release flavonoids that are detected by the rhizobial nodulation (Nod) protein NodD, initiating the transcriptional activation of nod genes and subsequent synthesis of Nod Factors (NFs). NFs then induce various legume responses essential for this symbiosis. Although evidence suggests differential regulation of nodD expression and NF biosynthesis during symbiosis, the necessity of this regulation for the formation of nitrogen-fixing nodules remains uncertain. Here, we demonstrate that deletion of the Rlv3841 NodD regulatory domain results in a constitutively active protein (NodDFI) capable of activating NF biosynthesis gene expression without the presence of flavonoids. Optimised constitutive expression of nodDFI or nodD3 in nodD null mutants led to wild-type levels of nodulation and nitrogen fixation in pea and M. truncatula, respectively, indicating that flavonoid-regulated nodD expression is not essential for supporting symbiosis. These findings illustrate that transcriptional control of flavonoid-independent NodD regulators can be employed to drive NF biosynthesis, which holds potential for engineering symbiosis between rhizobia and cereals equipped with reconstituted NF receptors.

Abstract Image

Abstract Image

黄酮类非依赖性结瘤基因调控根瘤菌结瘤基因支持与豆科植物的固氮共生
根瘤菌和豆科植物形成一种共生关系,导致形成被称为根瘤的根结构,细菌在根瘤中固定氮。豆科植物释放的黄酮类化合物可被根瘤菌结瘤蛋白NodD检测到,从而启动结瘤基因的转录激活和结瘤因子的合成。然后,NFs诱导这种共生关系所必需的各种豆类反应。尽管有证据表明共生过程中nodD表达和NF生物合成的差异调控,但这种调控对固氮结节形成的必要性仍不确定。在这里,我们证明了Rlv3841 NodD调控区域的缺失导致一个组成性活性蛋白(NodDFI)能够激活NF生物合成基因的表达,而不存在黄酮类化合物。nodD无效突变体中nodDFI或nodD3的优化组成表达分别导致豌豆和圆茎草的结瘤和固氮水平达到野生型水平,这表明黄酮类调控的nodD表达对支持共生并不是必需的。这些发现表明,不依赖于类黄酮的NodD调控因子的转录控制可以用来驱动NF的生物合成,这可能是根瘤菌与重组NF受体的谷物之间的工程共生的潜力。
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来源期刊
Environmental microbiology
Environmental microbiology 环境科学-微生物学
CiteScore
9.90
自引率
3.90%
发文量
427
审稿时长
2.3 months
期刊介绍: Environmental Microbiology provides a high profile vehicle for publication of the most innovative, original and rigorous research in the field. The scope of the Journal encompasses the diversity of current research on microbial processes in the environment, microbial communities, interactions and evolution and includes, but is not limited to, the following: the structure, activities and communal behaviour of microbial communities microbial community genetics and evolutionary processes microbial symbioses, microbial interactions and interactions with plants, animals and abiotic factors microbes in the tree of life, microbial diversification and evolution population biology and clonal structure microbial metabolic and structural diversity microbial physiology, growth and survival microbes and surfaces, adhesion and biofouling responses to environmental signals and stress factors modelling and theory development pollution microbiology extremophiles and life in extreme and unusual little-explored habitats element cycles and biogeochemical processes, primary and secondary production microbes in a changing world, microbially-influenced global changes evolution and diversity of archaeal and bacterial viruses new technological developments in microbial ecology and evolution, in particular for the study of activities of microbial communities, non-culturable microorganisms and emerging pathogens
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