{"title":"物理机制揭示了细菌在鞭毛数量超过临界值时速度减慢的原因","authors":"Maria Tătulea-Codrean, Eric Lauga","doi":"arxiv-2409.00574","DOIUrl":null,"url":null,"abstract":"Numerous studies have explored the link between bacterial swimming and the\nnumber of flagella, a distinguishing feature of motile multiflagellated\nbacteria. We revisit this open question using augmented slender-body theory\nsimulations, in which we resolve the full hydrodynamic interactions within a\nbundle of helical filaments rotating and translating in synchrony. Unlike\nprevious studies, our model considers the full torque-speed relationship of the\nbacterial flagellar motor, revealing its significant impact on multiflagellated\nswimming. Because the viscous load per motor decreases with flagellar number,\nthe bacterial flagellar motor (BFM) transitions from the high-load to the\nlow-load regime at a critical number of filaments, leading to bacterial\nslowdown as further flagella are added to the bundle. We explain the physical\nmechanism behind the observed slowdown as an interplay between the\nload-dependent generation of torque by the motor, and the load-reducing\ncooperativity between flagella, which consists of both hydrodynamic and\nnon-hydrodynamic components. The theoretically predicted critical number of\nflagella is remarkably close to the values reported for the model organism\n\\textit{Escherichia coli}. Our model further predicts that the critical number\nof flagella increases with viscosity, suggesting that bacteria can enhance\ntheir swimming capacity by growing more flagella in more viscous environments,\nconsistent with empirical observations.","PeriodicalId":501040,"journal":{"name":"arXiv - PHYS - Biological Physics","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2024-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Physical mechanism reveals bacterial slowdown above a critical number of flagella\",\"authors\":\"Maria Tătulea-Codrean, Eric Lauga\",\"doi\":\"arxiv-2409.00574\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Numerous studies have explored the link between bacterial swimming and the\\nnumber of flagella, a distinguishing feature of motile multiflagellated\\nbacteria. We revisit this open question using augmented slender-body theory\\nsimulations, in which we resolve the full hydrodynamic interactions within a\\nbundle of helical filaments rotating and translating in synchrony. Unlike\\nprevious studies, our model considers the full torque-speed relationship of the\\nbacterial flagellar motor, revealing its significant impact on multiflagellated\\nswimming. Because the viscous load per motor decreases with flagellar number,\\nthe bacterial flagellar motor (BFM) transitions from the high-load to the\\nlow-load regime at a critical number of filaments, leading to bacterial\\nslowdown as further flagella are added to the bundle. We explain the physical\\nmechanism behind the observed slowdown as an interplay between the\\nload-dependent generation of torque by the motor, and the load-reducing\\ncooperativity between flagella, which consists of both hydrodynamic and\\nnon-hydrodynamic components. The theoretically predicted critical number of\\nflagella is remarkably close to the values reported for the model organism\\n\\\\textit{Escherichia coli}. Our model further predicts that the critical number\\nof flagella increases with viscosity, suggesting that bacteria can enhance\\ntheir swimming capacity by growing more flagella in more viscous environments,\\nconsistent with empirical observations.\",\"PeriodicalId\":501040,\"journal\":{\"name\":\"arXiv - PHYS - Biological Physics\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-09-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"arXiv - PHYS - Biological Physics\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/arxiv-2409.00574\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"arXiv - PHYS - Biological Physics","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/arxiv-2409.00574","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Physical mechanism reveals bacterial slowdown above a critical number of flagella
Numerous studies have explored the link between bacterial swimming and the
number of flagella, a distinguishing feature of motile multiflagellated
bacteria. We revisit this open question using augmented slender-body theory
simulations, in which we resolve the full hydrodynamic interactions within a
bundle of helical filaments rotating and translating in synchrony. Unlike
previous studies, our model considers the full torque-speed relationship of the
bacterial flagellar motor, revealing its significant impact on multiflagellated
swimming. Because the viscous load per motor decreases with flagellar number,
the bacterial flagellar motor (BFM) transitions from the high-load to the
low-load regime at a critical number of filaments, leading to bacterial
slowdown as further flagella are added to the bundle. We explain the physical
mechanism behind the observed slowdown as an interplay between the
load-dependent generation of torque by the motor, and the load-reducing
cooperativity between flagella, which consists of both hydrodynamic and
non-hydrodynamic components. The theoretically predicted critical number of
flagella is remarkably close to the values reported for the model organism
\textit{Escherichia coli}. Our model further predicts that the critical number
of flagella increases with viscosity, suggesting that bacteria can enhance
their swimming capacity by growing more flagella in more viscous environments,
consistent with empirical observations.