Jang Hye-In, Kim Pyonghwa, Kim Yong-Ick
School of Cosmetic Science and Beauty Biotechnology, Semyung University, Jecheon 27136, Republic of Korea.
Department of Chemistry and Environmental Science, New Jersey Institute of Technology, Newark, New Jersey 07102, United States.
ACS Omega. 2023 Mar 14;8(12):10784-10788. doi: 10.1021/acsomega.2c06457. eCollection 2023 Mar 28.
Most organisms have circadian clocks to ensure the metabolic cycle to resonate with the rhythmic environmental changes without "damping," or losing robustness. Cyanobacteria is the oldest and simplest form of life that is known to harbor this biological intricacy. Its KaiABC-based central oscillator proteins can be reconstituted inside a test tube, and the post-translational modification cycle occurs with 24 h periodicity. KaiC's two major phosphorylation sites, Ser-431 and Thr-432, become phosphorylated and dephosphorylated by interacting with KaiA and KaiB, respectively. Here, we mutate Thr-432 into Ser to find the oscillatory phosphoryl transfer reaction damps. Previously, this mutant KaiC was reported to be arrhythmic in vivo. However, we found that the mutant KaiC gradually loses the ability to run in an autonomous manner and stays constitutively phosphorylated after 3 cycles in vitro.
大多数生物体都有生物钟,以确保代谢周期与有节奏的环境变化“同步”,而不会“衰减”或失去稳健性。蓝藻是已知拥有这种生物复杂性的最古老、最简单的生命形式。其基于KaiABC的中央振荡器蛋白可以在试管内重组,翻译后修饰周期以24小时为周期发生。KaiC的两个主要磷酸化位点Ser-431和Thr-432,分别通过与KaiA和KaiB相互作用而发生磷酸化和去磷酸化。在这里,我们将Thr-432突变为Ser,发现振荡性磷酸转移反应受到抑制。此前,据报道这种突变型KaiC在体内无节律。然而,我们发现突变型KaiC在体外经过3个周期后逐渐失去自主运行的能力,并持续处于磷酸化状态。