Bae Da-Woon, Lee Seong Hyuk, Park Ji Hye, Son Se-Young, Lin Yuxi, Lee Jung Hyen, Jang Bo-Ram, Lee Kyu-Ho, Lee Young-Ho, Lee Hyun Sook, Kang Sung Gyun, Kim Byoung Sik, Cha Sun-Shin
Department of Chemistry & Nanoscience, Ewha Womans University, Seoul 03760, Republic of Korea.
Marine Biotechnology Research Center, Korea Institute of Ocean Science and Technology, Busan, South Korea.
Nucleic Acids Res. 2023 Oct 13;51(18):10026-10040. doi: 10.1093/nar/gkad699.
Thermococcus onnurineus NA1, a hyperthermophilic carboxydotrophic archaeon, produces H2 through CO oxidation catalyzed by proteins encoded in a carbon monoxide dehydrogenase (CODH) gene cluster. TON_1525 with a DNA-binding helix-turn-helix (HTH) motif is a putative repressor regulating the transcriptional expression of the codh gene cluster. The T55I mutation in TON_1525 led to enhanced H2 production accompanied by the increased expression of genes in the codh cluster. Here, TON_1525 was demonstrated to be a dimer. Monomeric TON_1525 adopts a novel 'eighth note' symbol-like fold (referred to as 'eighth note' fold regulator, EnfR), and the dimerization mode of EnfR is unique in that it has no resemblance to structures in the Protein Data Bank. According to footprinting and gel shift assays, dimeric EnfR binds to a 36-bp pseudo-palindromic inverted repeat in the promoter region of the codh gene cluster, which is supported by an in silico EnfR/DNA complex model and mutational studies revealing the implication of N-terminal loops as well as HTH motifs in DNA recognition. The DNA-binding affinity of the T55I mutant was lowered by ∼15-fold, for which the conformational change of N-terminal loops is responsible. In addition, transcriptome analysis suggested that EnfR could regulate diverse metabolic processes besides H2 production.
嗜热栖热放线菌NA1是一种嗜热羧营养古菌,通过一氧化碳脱氢酶(CODH)基因簇编码的蛋白质催化的CO氧化产生H2。具有DNA结合螺旋-转角-螺旋(HTH)基序的TON_1525是一种推定的阻遏物,调节codh基因簇的转录表达。TON_1525中的T55I突变导致H2产量增加,同时codh簇中的基因表达增加。在这里,TON_1525被证明是一种二聚体。单体TON_1525采用一种新颖的“八分音符”符号样折叠(称为“八分音符”折叠调节因子,EnfR),EnfR的二聚化模式独特,因为它与蛋白质数据库中的结构没有相似之处。根据足迹和凝胶迁移试验,二聚体EnfR与codh基因簇启动子区域中的一个36 bp假回文反向重复序列结合,这得到了一个计算机模拟的EnfR/DNA复合物模型和突变研究的支持,该研究揭示了N端环以及HTH基序在DNA识别中的作用。T55I突变体的DNA结合亲和力降低了约15倍,这是由N端环的构象变化引起的。此外,转录组分析表明,EnfR除了调节H2产生外,还可以调节多种代谢过程。