2008 | Veening, Jan-Willem; Smits, Wiep Klaas; Kuipers, Oscar P.
The article discusses bistability, epigenetics, and bet-hedging in bacteria, focusing on how microbial populations exhibit phenotypic variation and how this variation can enhance survival. Bistability refers to the ability of cells to exist in two distinct states, often due to gene regulatory networks with positive feedback loops. Epigenetic inheritance allows cells to pass their state to the next generation, contributing to phenotypic variation. Bet-hedging is a strategy where bacteria diversify their phenotypes to increase survival under variable conditions.
The review highlights the role of bistable networks, epigenetic inheritance, and bet-hedging in bacterial behavior. It discusses examples such as competence development in *Bacillus subtilis*, where the key regulator ComK exhibits bistability. The study of *B. subtilis* sporulation shows that cells can switch between nonsporulating and sporulating states, with the decision influenced by epigenetic factors. The article also explores the use of synthetic biology to create genetic logic-AND gates, which can generate phenotypic heterogeneity.
Phenotypic variation is crucial for bacterial survival, especially under environmental stress. The review discusses how heterogeneity in exoprotease and biofilm matrix production in *B. subtilis* can be explained by complex regulatory networks. In *E. coli*, hypermutable subpopulations (HMS) can arise under stress conditions, contributing to genetic diversity. These subpopulations are regulated by factors such as the SOS response and RpoS, forming a logic-AND gate.
The article emphasizes that phenotypic variation is a bet-hedging strategy, ensuring that at least some cells survive under changing conditions. Bacterial persistence, where a small subpopulation of cells enters a dormant state, is another form of bet-hedging. The review concludes that understanding these mechanisms is essential for biotechnology and medical applications, as they can be harnessed to design synthetic circuits and improve bacterial functions.The article discusses bistability, epigenetics, and bet-hedging in bacteria, focusing on how microbial populations exhibit phenotypic variation and how this variation can enhance survival. Bistability refers to the ability of cells to exist in two distinct states, often due to gene regulatory networks with positive feedback loops. Epigenetic inheritance allows cells to pass their state to the next generation, contributing to phenotypic variation. Bet-hedging is a strategy where bacteria diversify their phenotypes to increase survival under variable conditions.
The review highlights the role of bistable networks, epigenetic inheritance, and bet-hedging in bacterial behavior. It discusses examples such as competence development in *Bacillus subtilis*, where the key regulator ComK exhibits bistability. The study of *B. subtilis* sporulation shows that cells can switch between nonsporulating and sporulating states, with the decision influenced by epigenetic factors. The article also explores the use of synthetic biology to create genetic logic-AND gates, which can generate phenotypic heterogeneity.
Phenotypic variation is crucial for bacterial survival, especially under environmental stress. The review discusses how heterogeneity in exoprotease and biofilm matrix production in *B. subtilis* can be explained by complex regulatory networks. In *E. coli*, hypermutable subpopulations (HMS) can arise under stress conditions, contributing to genetic diversity. These subpopulations are regulated by factors such as the SOS response and RpoS, forming a logic-AND gate.
The article emphasizes that phenotypic variation is a bet-hedging strategy, ensuring that at least some cells survive under changing conditions. Bacterial persistence, where a small subpopulation of cells enters a dormant state, is another form of bet-hedging. The review concludes that understanding these mechanisms is essential for biotechnology and medical applications, as they can be harnessed to design synthetic circuits and improve bacterial functions.