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绿藻新突变营养缺陷型对 B 元素缺乏的响应。

Responses of a Newly Evolved Auxotroph of Chlamydomonas to B Deprivation.

机构信息

Department of Plant Sciences, University of Cambridge, Downing Street, Cambridge, CB2 3EA, United Kingdom.

Marine Biological Association of the United Kingdom, Citadel Hill, Plymouth EX4 4PY, United Kingdom.

出版信息

Plant Physiol. 2020 May;183(1):167-178. doi: 10.1104/pp.19.01375. Epub 2020 Feb 20.

DOI:10.1104/pp.19.01375
PMID:32079734
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7210614/
Abstract

The corrinoid B is synthesized only by prokaryotes yet is widely required by eukaryotes as an enzyme cofactor. Microalgae have evolved B dependence on multiple occasions, and we previously demonstrated that experimental evolution of the non-B-requiring alga in media supplemented with B generated a B-dependent mutant (hereafter metE7). This clone provides a unique opportunity to study the physiology of a nascent B auxotroph. Our analyses demonstrate that B deprivation of metE7 disrupts C1 metabolism, causes an accumulation of starch and triacylglycerides, and leads to a decrease in photosynthetic pigments, proteins, and free amino acids. B deprivation also caused a substantial increase in reactive oxygen species, which preceded rapid cell death. Survival could be improved without compromising growth by simultaneously depriving the cells of nitrogen, suggesting a type of cross protection. Significantly, we found further improvements in survival under B limitation and an increase in B use efficiency after metE7 underwent a further period of experimental evolution, this time in coculture with a B-producing bacterium. Therefore, although an early B-dependent alga would likely be poorly adapted to coping with B deprivation, association with B-producers can ensure long-term survival whilst also providing a suitable environment for evolving mechanisms to tolerate B limitation better.

摘要

钴胺素 B 仅由原核生物合成,但真核生物广泛将其作为酶辅因子。微藻已经多次进化出对 B 的依赖,我们之前证明,在补充 B 的培养基中对非 B 需求的藻类进行实验进化,会产生一个依赖 B 的突变体(以下简称 metE7)。这个克隆为研究新出现的 B 营养缺陷型的生理学提供了一个独特的机会。我们的分析表明,metE7 的 B 缺乏会破坏 C1 代谢,导致淀粉和三酰基甘油的积累,并导致光合色素、蛋白质和游离氨基酸减少。B 缺乏还导致活性氧的大量增加,这先于快速的细胞死亡。在不影响生长的情况下,同时剥夺细胞氮,可以显著提高存活率,表明存在一种交叉保护。重要的是,我们发现 metE7 在与产生 B 的细菌共培养的情况下,经过进一步的实验进化后,在 B 限制下的存活率进一步提高,B 利用效率也提高了。因此,尽管早期依赖 B 的藻类可能很难适应 B 缺乏,但与 B 生产者的联系可以确保长期生存,同时为进化出更好地耐受 B 限制的机制提供了合适的环境。