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芽殖氨基酸的分解代谢对于防止 在过早的孢子萌发是必需的。

Catabolism of germinant amino acids is required to prevent premature spore germination in .

机构信息

Max Planck Institute for Evolutionary Biology, Plön, Germany.

出版信息

mBio. 2024 May 8;15(5):e0056224. doi: 10.1128/mbio.00562-24. Epub 2024 Apr 2.

DOI:10.1128/mbio.00562-24
PMID:38564667
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11077977/
Abstract

UNLABELLED

Spores of germinate in response to specific germinant molecules that are recognized by receptors in the spore envelope. Germinants signal to the dormant spore that the environment can support vegetative growth, so many germinants, such as alanine and valine, are also essential metabolites. As such, they are also required to build the spore. Here we show that these germinants cause premature germination if they are still present at the latter stages of spore formation and beyond, but that metabolism is configured to prevent this: alanine and valine are catabolized and cleared from wild-type cultures even when alternative carbon and nitrogen sources are present. Alanine and valine accumulate in the spent media of mutants that are unable to catabolize these amino acids, and premature germination is pervasive. Premature germination does not occur if the germinant receptor that responds to alanine and valine is eliminated, or if wild-type strains that are able to catabolize and clear alanine and valine are also present in coculture. Our findings demonstrate that spore-forming bacteria must fine-tune the concentration of any metabolite that can also function as a germinant to a level that is high enough to allow for spore development to proceed, but not so high as to promote premature germination. These results indicate that germinant selection and metabolism are tightly linked, and suggest that germinant receptors evolve in tandem with the catabolic priorities of the spore-forming bacterium.

IMPORTANCE

Many bacterial species produce dormant cells called endospores, which are not killed by antibiotics or common disinfection practices. Endospores pose critical challenges in the food industry, where endospore contaminations cause food spoilage, and in hospitals, where infections by pathogenic endospore formers threaten the life of millions every year. Endospores lose their resistance properties and can be killed easily when they germinate and exit dormancy. We have discovered that the enzymes that break down the amino acids alanine and valine are critical for the production of stable endospores. If these enzymes are absent, endospores germinate as they are formed or shortly thereafter in response to alanine, which can initiate the germination of many different species' endospores, or to valine. By blocking the activity of alanine dehydrogenase, the enzyme that breaks down alanine and is not present in mammals, it may be possible to inactivate endospores by triggering premature and unproductive germination.

摘要

未标记

孢子在休眠状态下对环境没有反应,只有在接收到特定的发芽分子(被孢子囊上的受体识别)后才会发芽。发芽分子向休眠的孢子发出环境可以支持营养生长的信号,因此许多发芽分子(如丙氨酸和缬氨酸)也是必需的代谢物。因此,它们也是构建孢子所必需的。在这里,我们表明,如果这些发芽分子在孢子形成的后期仍然存在,甚至在更晚的阶段存在,它们会导致过早发芽,但新陈代谢会被配置来防止这种情况发生:即使存在替代的碳和氮源,丙氨酸和缬氨酸也会在野生型培养物中被分解代谢并清除。在无法分解这些氨基酸的突变体的耗尽培养基中积累丙氨酸和缬氨酸,并且广泛存在过早发芽。如果消除了响应丙氨酸和缬氨酸的发芽受体,或者如果能够分解代谢和清除丙氨酸和缬氨酸的野生型菌株也存在于共培养物中,则不会发生过早发芽。我们的研究结果表明,产孢子细菌必须将任何可以作为发芽分子的代谢物的浓度精确调整到足以允许孢子发育进行的水平,但又不能高到促进过早发芽的水平。这些结果表明发芽分子的选择和代谢紧密相关,并表明发芽受体与产孢子细菌的分解代谢优先级协同进化。

重要性

许多细菌物种产生休眠细胞,称为芽孢,抗生素或常见的消毒措施都无法杀死芽孢。芽孢在食品工业中构成了严重的挑战,因为芽孢污染会导致食物变质,而在医院中,每年由致病性芽孢形成菌引起的感染会威胁数百万人的生命。当芽孢发芽并脱离休眠状态时,它们会失去其抗性特性,并且很容易被杀死。我们发现,分解丙氨酸和缬氨酸的酶对于稳定芽孢的产生至关重要。如果这些酶不存在,芽孢会在形成时或形成后不久响应丙氨酸而发芽,这可能会引发许多不同物种的芽孢发芽,或者响应缬氨酸而发芽。通过阻断分解丙氨酸的酶丙氨酸脱氢酶的活性,而该酶在哺乳动物中不存在,通过触发过早和无效的发芽,可能可以使芽孢失活。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c8a/11077977/ba9329eae3ca/mbio.00562-24.f007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c8a/11077977/0e528e2c7d44/mbio.00562-24.f001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c8a/11077977/31a4a3ba2911/mbio.00562-24.f002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c8a/11077977/86f7c0014979/mbio.00562-24.f003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c8a/11077977/0551c26fb728/mbio.00562-24.f004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c8a/11077977/f4f3f75f8856/mbio.00562-24.f005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c8a/11077977/3f677441999b/mbio.00562-24.f006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c8a/11077977/ba9329eae3ca/mbio.00562-24.f007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c8a/11077977/0e528e2c7d44/mbio.00562-24.f001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c8a/11077977/31a4a3ba2911/mbio.00562-24.f002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c8a/11077977/86f7c0014979/mbio.00562-24.f003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c8a/11077977/0551c26fb728/mbio.00562-24.f004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c8a/11077977/f4f3f75f8856/mbio.00562-24.f005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c8a/11077977/3f677441999b/mbio.00562-24.f006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c8a/11077977/ba9329eae3ca/mbio.00562-24.f007.jpg

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