Oral Biology, School of Dental Sciences, Newcastle University, Newcastle upon Tyne, UK.
Lett Appl Microbiol. 2013 Dec;57(6):467-75. doi: 10.1111/lam.12134. Epub 2013 Aug 1.
The death and lysis of microbial cells leads to the release of cytoplasmic contents, many of which are rapidly degraded by enzymes. However, some macromolecules survive intact and find new functions in the extracellular environment. There is now strong evidence that DNA released from cells during lysis, or sometimes by active secretion, becomes a key component of the macromolecular scaffold in many different biofilms. Enzymatic degradation of extracellular DNA can weaken the biofilm structure and release microbial cells from the surface. Many bacteria produce extracellular deoxyribonuclease (DNase) enzymes that are apparently tightly regulated to avoid excessive degradation of the biofilm matrix. Interfering with these control mechanisms, or adding exogenous DNases, could prove a potent strategy for controlling biofilm growth.
微生物细胞的死亡和裂解会导致细胞质内容物的释放,其中许多内容物很快被酶降解。然而,一些大分子完整地存活下来,并在细胞外环境中找到新的功能。现在有强有力的证据表明,细胞裂解时或有时通过主动分泌释放的细胞内 DNA 成为许多不同生物膜中大分子支架的关键组成部分。细胞外 DNA 的酶促降解会削弱生物膜结构,并使微生物细胞从表面释放。许多细菌产生胞外脱氧核糖核酸酶(DNase),这些酶显然受到严格调控,以避免生物膜基质的过度降解。干扰这些控制机制,或添加外源性 DNases,可能是控制生物膜生长的有效策略。