Stephen J Knabel, Ramaswamy Anantheswaran, Aubrey Mendonca, Wei Zhang
{"title":"毒素-抗毒素和sigma因子可以通过一个综合的营养反应控制系统优化自由生活细菌在整个生命周期中的适应性。","authors":"Stephen J Knabel, Ramaswamy Anantheswaran, Aubrey Mendonca, Wei Zhang","doi":"10.1098/rsif.2025.0185","DOIUrl":null,"url":null,"abstract":"<p><p>Toxin-antitoxin systems (TASs) are ubiquitous in the chromosomes of free-living bacteria, yet their primary biological function remains poorly understood. Bacteria reproduce exponentially via 2<sup><i>n</i></sup> growth kinetics and thus must respond to changing nutrient availability to reproduce rapidly during short periods of feast and survive during long periods of famine. Type II TASs represent stable enzyme-unstable inhibitor systems that are regulated by reversible competitive inhibition, which allows them to efficiently produce pleiotropic effects on prokaryotic cells in a continuous (analogue) manner due to varying concentrations of free toxin throughout the life cycle. A nutrient-responsive cybernetic system (NRCS) model is proposed where intracellular nutrient concentration feeds back to control the emergent properties of growth, death and growth/death arrest, which results in a novel fitness strategy termed K Sensing and Control. When nutrients become limiting, alternative general stress response sigma factors Ϭ<sup>S</sup> and Ϭ<sup>B</sup> regulate the expression of hundreds of genes that may control the transformation of vegetative bacteria into coccoid, stress-tolerant 'motherspores'. An integrated NRCS model is presented that shows how TASs and sigma factors may work in concert to efficiently regulate population dynamics, cellular physiology and cellular differentiation throughout the life cycle, which optimizes the biological fitness of free-living bacteria.</p>","PeriodicalId":17488,"journal":{"name":"Journal of The Royal Society Interface","volume":"22 230","pages":"20250185"},"PeriodicalIF":3.5000,"publicationDate":"2025-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12440627/pdf/","citationCount":"0","resultStr":"{\"title\":\"Toxin-antitoxins and sigma factors may optimize the fitness of free-living bacteria throughout the life cycle via an integrated nutrient-responsive cybernetic system.\",\"authors\":\"Stephen J Knabel, Ramaswamy Anantheswaran, Aubrey Mendonca, Wei Zhang\",\"doi\":\"10.1098/rsif.2025.0185\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Toxin-antitoxin systems (TASs) are ubiquitous in the chromosomes of free-living bacteria, yet their primary biological function remains poorly understood. Bacteria reproduce exponentially via 2<sup><i>n</i></sup> growth kinetics and thus must respond to changing nutrient availability to reproduce rapidly during short periods of feast and survive during long periods of famine. Type II TASs represent stable enzyme-unstable inhibitor systems that are regulated by reversible competitive inhibition, which allows them to efficiently produce pleiotropic effects on prokaryotic cells in a continuous (analogue) manner due to varying concentrations of free toxin throughout the life cycle. A nutrient-responsive cybernetic system (NRCS) model is proposed where intracellular nutrient concentration feeds back to control the emergent properties of growth, death and growth/death arrest, which results in a novel fitness strategy termed K Sensing and Control. When nutrients become limiting, alternative general stress response sigma factors Ϭ<sup>S</sup> and Ϭ<sup>B</sup> regulate the expression of hundreds of genes that may control the transformation of vegetative bacteria into coccoid, stress-tolerant 'motherspores'. An integrated NRCS model is presented that shows how TASs and sigma factors may work in concert to efficiently regulate population dynamics, cellular physiology and cellular differentiation throughout the life cycle, which optimizes the biological fitness of free-living bacteria.</p>\",\"PeriodicalId\":17488,\"journal\":{\"name\":\"Journal of The Royal Society Interface\",\"volume\":\"22 230\",\"pages\":\"20250185\"},\"PeriodicalIF\":3.5000,\"publicationDate\":\"2025-09-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12440627/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of The Royal Society Interface\",\"FirstCategoryId\":\"103\",\"ListUrlMain\":\"https://doi.org/10.1098/rsif.2025.0185\",\"RegionNum\":2,\"RegionCategory\":\"综合性期刊\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/9/17 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q1\",\"JCRName\":\"MULTIDISCIPLINARY SCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of The Royal Society Interface","FirstCategoryId":"103","ListUrlMain":"https://doi.org/10.1098/rsif.2025.0185","RegionNum":2,"RegionCategory":"综合性期刊","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/9/17 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"MULTIDISCIPLINARY SCIENCES","Score":null,"Total":0}
Toxin-antitoxins and sigma factors may optimize the fitness of free-living bacteria throughout the life cycle via an integrated nutrient-responsive cybernetic system.
Toxin-antitoxin systems (TASs) are ubiquitous in the chromosomes of free-living bacteria, yet their primary biological function remains poorly understood. Bacteria reproduce exponentially via 2n growth kinetics and thus must respond to changing nutrient availability to reproduce rapidly during short periods of feast and survive during long periods of famine. Type II TASs represent stable enzyme-unstable inhibitor systems that are regulated by reversible competitive inhibition, which allows them to efficiently produce pleiotropic effects on prokaryotic cells in a continuous (analogue) manner due to varying concentrations of free toxin throughout the life cycle. A nutrient-responsive cybernetic system (NRCS) model is proposed where intracellular nutrient concentration feeds back to control the emergent properties of growth, death and growth/death arrest, which results in a novel fitness strategy termed K Sensing and Control. When nutrients become limiting, alternative general stress response sigma factors ϬS and ϬB regulate the expression of hundreds of genes that may control the transformation of vegetative bacteria into coccoid, stress-tolerant 'motherspores'. An integrated NRCS model is presented that shows how TASs and sigma factors may work in concert to efficiently regulate population dynamics, cellular physiology and cellular differentiation throughout the life cycle, which optimizes the biological fitness of free-living bacteria.
期刊介绍:
J. R. Soc. Interface welcomes articles of high quality research at the interface of the physical and life sciences. It provides a high-quality forum to publish rapidly and interact across this boundary in two main ways: J. R. Soc. Interface publishes research applying chemistry, engineering, materials science, mathematics and physics to the biological and medical sciences; it also highlights discoveries in the life sciences of relevance to the physical sciences. Both sides of the interface are considered equally and it is one of the only journals to cover this exciting new territory. J. R. Soc. Interface welcomes contributions on a diverse range of topics, including but not limited to; biocomplexity, bioengineering, bioinformatics, biomaterials, biomechanics, bionanoscience, biophysics, chemical biology, computer science (as applied to the life sciences), medical physics, synthetic biology, systems biology, theoretical biology and tissue engineering.