Department of Chemical Engineering, Texas A & M University, College Station, TX 77843-3122, USA.
Microb Biotechnol. 2010 Nov;3(6):717-28. doi: 10.1111/j.1751-7915.2010.00220.x.
The global transcriptional regulator Hha of Escherichia coli controls biofilm formation and virulence. Previously, we showed that Hha decreases initial biofilm formation; here, we engineered Hha for two goals: to increase biofilm dispersal and to reduce biofilm formation. Using random mutagenesis, Hha variant Hha13D6 (D22V, L40R, V42I and D48A) was obtained that causes nearly complete biofilm dispersal (96%) by increasing apoptosis without affecting initial biofilm formation. Hha13D6 caused cell death probably by the activation of proteases since Hha-mediated dispersal was dependent on protease HslV. Hha variant Hha24E9 (K62X) was also obtained that decreased biofilm formation by inducing gadW, glpT and phnF but that did not alter biofilm dispersal. Hence, Hha may be engineered to influence both biofilm dispersal and formation.
大肠杆菌的全局转录调节剂 Hha 控制生物膜的形成和毒力。先前,我们表明 Hha 减少初始生物膜的形成;在这里,我们设计了 Hha 的两个目标:增加生物膜的分散和减少生物膜的形成。使用随机诱变,获得了 Hha 变体 Hha13D6(D22V、L40R、V42I 和 D48A),通过增加细胞凋亡而不影响初始生物膜的形成,导致几乎完全的生物膜分散(96%)。Hha13D6 引起细胞死亡可能是通过激活蛋白酶引起的,因为 Hha 介导的分散依赖于蛋白酶 HslV。还获得了 Hha 变体 Hha24E9(K62X),它通过诱导 gadW、glpT 和 phnF 减少生物膜的形成,但不改变生物膜的分散。因此,Hha 可以被设计来影响生物膜的分散和形成。