Ponnampalam S N, Elsen S, Bauer C E
Biochemistry Program, Department of Chemistry, Indiana University, Bloomington, Indiana 47405, USA.
J Biol Chem. 1998 Nov 13;273(46):30757-61. doi: 10.1074/jbc.273.46.30757.
Previous studies demonstrated that bacteriochlorophyll, carotenoid, and light harvesting gene expression in Rhodobacter capsulatus is repressed under aerobic growth conditions by the repressor CrtJ. Isolated CrtJ is known to bind to the palindrome TGTN12ACA, which is present in two copies in the bchC promoter, one of which spans the -35 and the other the -10 sigma-70 recognition sequences. In this study, we demonstrate that CrtJ binds to the two palindromic sites in the bchC promoter in a cooperative manner. The level of cooperativity of CrtJ binding to the -35 palindrome was shown to be 26-fold. A distance of 8 base pairs between the two palindromic sites was shown to be critical for cooperative binding, as evidenced by the disruption of binding that resulted when +6 and +11 base pairs were inserted between the palindromes.
先前的研究表明,在需氧生长条件下,荚膜红细菌中的细菌叶绿素、类胡萝卜素和光捕获基因表达受阻遏物CrtJ的抑制。已知分离出的CrtJ可与回文序列TGTN12ACA结合,该序列在bchC启动子中有两个拷贝,其中一个跨越-35区,另一个跨越-10区的σ-70识别序列。在本研究中,我们证明CrtJ以协同方式结合到bchC启动子中的两个回文位点。CrtJ与-35回文序列结合的协同水平显示为26倍。两个回文位点之间8个碱基对的距离对协同结合至关重要,这一点可通过在回文序列之间插入+6和+11个碱基对导致结合被破坏得到证明。