Calcium and the ecology of photosynthesis in purple sulfur bacteria

IF 4.3 2区 生物学 Q2 MICROBIOLOGY
Michael T. Madigan, W. Matthew Sattley, Yukihiro Kimura, Zheng-Yu Wang-Otomo
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Abstract

The ecological success of purple sulfur bacteria (PSB) is linked to their ability to collect near-infrared solar energy by membrane-integrated, pigment–protein photocomplexes. These include a Core complex containing both light-harvesting 1 (LH1) and reaction centre (RC) components (called the LH1–RC photocomplex) present in all PSB and a peripheral light-harvesting complex present in most but not all PSB. In research to explain the unusual absorption properties of the thermophilic purple sulfur bacterium Thermochromatium tepidum, Ca2+ was discovered bound to LH1 polypeptides in its LH1–RC; further work showed that calcium controls both the thermostability and unusual spectrum of the Core complex. Since then, Ca2+ has been found in the LH1–RC photocomplexes of several other PSB, including mesophilic species, but not in the LH1–RC of purple non-sulfur bacteria. Here we focus on four species of PSB—two thermophilic and two mesophilic—and describe how Ca2+ is integrated into and affects their photosynthetic machinery and why this previously overlooked divalent metal is a key nutrient for their ecological success.

Abstract Image

Abstract Image

钙与紫硫细菌光合作用生态学
紫硫细菌(PSB)在生态学上的成功与它们通过膜整合色素-蛋白质光复合体收集近红外太阳能的能力有关。这些光复合体包括存在于所有 PSB 中的包含光收集 1(LH1)和反应中心(RC)成分的核心复合体(称为 LH1-RC 光复合体),以及存在于大多数但并非所有 PSB 中的外围光收集复合体。在解释嗜热紫硫细菌 Thermochromatium tepidum 的不寻常吸收特性的研究中,发现 Ca2+ 与 LH1-RC 中的 LH1 多肽结合;进一步的研究表明,钙控制着核心复合体的恒温性和不寻常光谱。此后,在其他几种 PSB(包括嗜中性物种)的 LH1-RC 光复合体中也发现了 Ca2+,但在紫色非硫细菌的 LH1-RC 中却没有发现。在此,我们重点研究了四种 PSB--两种嗜热菌和两种嗜中菌--并描述了 Ca2+ 如何整合到它们的光合作用机制中并对其产生影响,以及为什么这种以前被忽视的二价金属是它们生态成功的关键营养物质。
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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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