If ATP and macromolecular synthesis are needed for dormant spores of Bacillota species to trigger spore germination, where do the energy and precursors come from?
IF 3.2 3区 生物学Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
{"title":"If ATP and macromolecular synthesis are needed for dormant spores of Bacillota species to trigger spore germination, where do the energy and precursors come from?","authors":"Peter Setlow, Graham Christie","doi":"10.1093/jambio/lxaf177","DOIUrl":null,"url":null,"abstract":"<p><p>ATP is one of the signature molecules of life. As the primary energy currency of cells, the debate concerning its involvement, if any, in driving the earliest biophysical events associated with germination of dormant Bacillota spores has continued without resolution for several decades. With a view to framing the debate, this article presents a synopsis of fundamental aspects of spore physiology coupled with key experimental observations in the context of bioenergetics and macromolecular synthesis. Evidently, neither the spore core nor the inner membrane present sub-cellular environments conducive to significant oxidative- or substrate-level phosphorylation, gene transcription, or protein translation activities. Additionally, neither the precursors of numerous critical macromolecules, nor the cellular apparatus required to synthesize these precursors, are present in dormant spores. Even if these might somehow be generated within localized micro-environments, the phosphorylation potential associated with the negligible quantities of ATP present in spores is severely reduced relative to actively metabolizing cells as a result of spores' sub-optimal adenylate energy charge. Thus, the scope for significant macromolecular synthesis is thermodynamically improbable. Looking ahead, clarity in the field of spore bioenergetics and metabolism will only be achieved by studies that unambiguously encompass the physiological constraints imposed by these most resolute cells.</p>","PeriodicalId":15036,"journal":{"name":"Journal of Applied Microbiology","volume":" ","pages":""},"PeriodicalIF":3.2000,"publicationDate":"2025-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Applied Microbiology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1093/jambio/lxaf177","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"BIOTECHNOLOGY & APPLIED MICROBIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
ATP is one of the signature molecules of life. As the primary energy currency of cells, the debate concerning its involvement, if any, in driving the earliest biophysical events associated with germination of dormant Bacillota spores has continued without resolution for several decades. With a view to framing the debate, this article presents a synopsis of fundamental aspects of spore physiology coupled with key experimental observations in the context of bioenergetics and macromolecular synthesis. Evidently, neither the spore core nor the inner membrane present sub-cellular environments conducive to significant oxidative- or substrate-level phosphorylation, gene transcription, or protein translation activities. Additionally, neither the precursors of numerous critical macromolecules, nor the cellular apparatus required to synthesize these precursors, are present in dormant spores. Even if these might somehow be generated within localized micro-environments, the phosphorylation potential associated with the negligible quantities of ATP present in spores is severely reduced relative to actively metabolizing cells as a result of spores' sub-optimal adenylate energy charge. Thus, the scope for significant macromolecular synthesis is thermodynamically improbable. Looking ahead, clarity in the field of spore bioenergetics and metabolism will only be achieved by studies that unambiguously encompass the physiological constraints imposed by these most resolute cells.
期刊介绍:
Journal of & Letters in Applied Microbiology are two of the flagship research journals of the Society for Applied Microbiology (SfAM). For more than 75 years they have been publishing top quality research and reviews in the broad field of applied microbiology. The journals are provided to all SfAM members as well as having a global online readership totalling more than 500,000 downloads per year in more than 200 countries. Submitting authors can expect fast decision and publication times, averaging 33 days to first decision and 34 days from acceptance to online publication. There are no page charges.