Ansaldi M, Jourlin-Castelli C, Lepelletier M, Théraulaz L, Méjean V
Laboratoire de Chimie Bactérienne, Institut de Biologie Structurale et Microbiologie, Centre National de la Recherche Scientifique, 13402 Marseille Cedex 20, France.
J Bacteriol. 2001 Apr;183(8):2691-5. doi: 10.1128/JB.183.8.2691-2695.2001.
Induction of the torCAD operon, encoding the trimethylamine N-oxide (TMAO) respiratory system, is tightly controlled by the TorS-TorR phosphorelay system in response to TMAO availability. TorS is an unorthodox sensor that contains three phosphorylation sites and transphosphorylates TorR via a four-step phosphorelay, His443-->Asp723-->His850-->Asp(TorR). In this study, we provide genetic evidence that TorS can dephosphorylate phospho-TorR when TMAO is removed. Dephosphorylation probably occurs by a reverse phosphorelay, Asp(TorR)-->His850-->Asp723, since His850 and Asp723 are both essential in this process. By using reverse transcriptase PCR, we also show that TMAO removal results in shutoff of tor operon transcription in less than 2 min. Based on our results and on analogy to other phosphorelay signal transduction systems, we propose that reverse phosphotransfer could be a rapid and efficient mechanism to inactivate response regulators.
编码三甲胺 N-氧化物(TMAO)呼吸系统的 torCAD 操纵子的诱导,受 TorS-TorR 磷酸化传递系统严格控制,以响应 TMAO 的可用性。TorS 是一种非传统传感器,含有三个磷酸化位点,并通过四步磷酸化传递(His443→Asp723→His850→Asp(TorR))将磷酸基团转移给 TorR。在本研究中,我们提供了遗传学证据,表明当去除 TMAO 时,TorS 可以使磷酸化的 TorR 去磷酸化。去磷酸化可能通过反向磷酸化传递(Asp(TorR)→His850→Asp723)发生,因为 His850 和 Asp723 在这个过程中都是必不可少的。通过使用逆转录酶 PCR,我们还表明,去除 TMAO 会导致 tor 操纵子转录在不到 2 分钟内关闭。基于我们的结果,并与其他磷酸化传递信号转导系统进行类比,我们提出反向磷酸转移可能是一种快速有效的机制,用于使响应调节因子失活。