Sulphur-Acquisition Pathways for Cysteine Synthesis Confer a Fitness Advantage to Bacteria in Plant Extracts

IF 4 2区 生物学 Q2 MICROBIOLOGY
Kazuya Ishikawa, Saki Yamaguchi, Taketo Tsukaoka, Makoto Tsunoda, Kazuyuki Furuta, Chikara Kaito
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Abstract

Bacteria and plants are closely associated with human society, in fields such as agriculture, public health, the food industry, and waste disposal. Bacteria have evolved nutrient-utilisation systems adapted to achieve the most efficient growth in their major habitats. However, empirical evidence to support the significance of bacterial nutrient utilisation in adaptation to plants is limited. Therefore, we investigated the genetic and nutritional factors required for bacterial growth in plant extracts by screening an Escherichia coli gene-knockout library in vegetable-based medium. Mutants lacking genes involved in sulphur assimilation, whereby sulphur is transferred from sulphate to cysteine, exhibited negligible growth in vegetable-based medium or plant extracts, owing to the low cysteine levels. The reverse transsulphuration pathway from methionine, another pathway for donating sulphur to cysteine, occurring in bacteria such as Bacillus subtilis, also played an important role in growth in plant extracts. These two sulphur-assimilation pathways were more frequently observed in plant-associated than in animal-associated bacteria. Sulphur-acquisition pathways for cysteine synthesis thus play a key role in bacterial growth in plant-derived environments such as plant residues and plant exudates.

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半胱氨酸合成的硫获取途径赋予细菌在植物提取物中的适应性优势
细菌和植物在农业、公共卫生、食品工业和废物处理等领域与人类社会密切相关。细菌已经进化出了适应其主要栖息地的营养利用系统,以实现最有效的生长。然而,支持细菌养分利用在适应植物中的重要性的经验证据有限。因此,我们通过筛选以蔬菜为基础的培养基中的大肠杆菌基因敲除文库来研究细菌在植物提取物中生长所需的遗传和营养因子。缺乏硫同化基因的突变体,硫从硫酸盐转移到半胱氨酸,由于半胱氨酸水平低,在蔬菜培养基或植物提取物中表现出微不足道的生长。从蛋氨酸到半胱氨酸的另一种将硫提供给枯草芽孢杆菌等细菌的反向转硫途径,在植物提取物的生长中也发挥了重要作用。这两种硫同化途径在植物相关细菌中比在动物相关细菌中更常见。因此,半胱氨酸合成的硫获取途径在植物源性环境(如植物残留物和植物渗出液)中的细菌生长中起着关键作用。
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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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