在无机碳限制下,Nostoc sp.和Agrobacterium sp.的相互作用由竞争和相互依赖决定。

IF 7.8 1区 生物学 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Jonna E Teikari, David A Russo, Markus Heuser, Otto Baumann, Julie A Z Zedler, Anton Liaimer, Elke Dittmann
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引用次数: 0

摘要

蓝藻属能够与植物形成共生关系,但也作为异养细菌的枢纽。通过比较无氧菌株Nostoc点状菌PCC 73102和xenic菌株Nostoc sp. KVJ2和KVJ3,我们能够证明在碳限制条件下蓝藻对异养伴侣几乎是专性的依赖。利用鸟枪蛋白质组学和显微镜技术对点状芽孢杆菌和农杆菌之间的亲密关系进行了详细分析,揭示了一种复杂的伙伴关系,其特征是对铁的竞争和对碳的促进。固定碳酶RubisCO普遍存在于糖体外,这表明点状芽孢杆菌中存在一种弱的碳浓缩机制,迫使其依赖于异养细菌。我们的研究表明共生Nostoc菌株具有有限的自主性,这也可以解释它对共生相互作用的偏好。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Competition and interdependence define interactions of Nostoc sp. and Agrobacterium sp. under inorganic carbon limitation.

Cyanobacteria of the Nostoc genus are capable of forming symbiotic relationships with plants but also serve as a hub for heterotrophic bacteria. By comparing the axenic strain Nostoc punctiforme PCC 73102 and the xenic strains Nostoc sp. KVJ2 and KVJ3, we were able to demonstrate an almost obligate dependence of the cyanobacteria on the heterotrophic partners under carbon-limiting conditions. A detailed analysis of the intimate relationship between N. punctiforme and the isolate Agrobacterium tumefaciens Het4 using shotgun proteomics and microscopy uncovered a complex partnership characterized by competition for iron and facilitation for carbon. The prevalent extracarboxysomal localization of the carbon-fixing enzyme RubisCO suggests that a weak carbon-concentrating mechanism in N. punctiforme enforces a dependence on heterotrophic bacteria. Our study indicates a limited autonomy of symbiotic Nostoc strains, which may also explain its preference for symbiotic interactions.

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来源期刊
npj Biofilms and Microbiomes
npj Biofilms and Microbiomes Immunology and Microbiology-Microbiology
CiteScore
12.10
自引率
3.30%
发文量
91
审稿时长
9 weeks
期刊介绍: npj Biofilms and Microbiomes is a comprehensive platform that promotes research on biofilms and microbiomes across various scientific disciplines. The journal facilitates cross-disciplinary discussions to enhance our understanding of the biology, ecology, and communal functions of biofilms, populations, and communities. It also focuses on applications in the medical, environmental, and engineering domains. The scope of the journal encompasses all aspects of the field, ranging from cell-cell communication and single cell interactions to the microbiomes of humans, animals, plants, and natural and built environments. The journal also welcomes research on the virome, phageome, mycome, and fungome. It publishes both applied science and theoretical work. As an open access and interdisciplinary journal, its primary goal is to publish significant scientific advancements in microbial biofilms and microbiomes. The journal enables discussions that span multiple disciplines and contributes to our understanding of the social behavior of microbial biofilm populations and communities, and their impact on life, human health, and the environment.
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