Ogawa N, McFall S M, Klem T J, Miyashita K, Chakrabarty A M
National Institute of Agro-Environmental Sciences, Tsukuba, Ibaraki 305-8604, Japan.
J Bacteriol. 1999 Nov;181(21):6697-705. doi: 10.1128/JB.181.21.6697-6705.1999.
Ralstonia eutropha (formerly Alcaligenes eutrophus) NH9 degrades 3-chlorobenzoate via the modified ortho-cleavage pathway. A ca. 5.7-kb six-gene cluster is responsible for chlorocatechol degradation: the cbnABCD operon encoding the degradative enzymes (including orfX of unknown function) and the divergently transcribed cbnR gene encoding the LysR-type transcriptional regulator of the cbn operon. The cbnRAB orfXCD gene cluster is nearly identical to the chlorocatechol genes (tcbRCD orfXEF) of the 1,2, 4-trichlorobenzene-degrading bacterium Pseudomonas sp. strain P51. Transcriptional fusion studies demonstrated that cbnR regulates the expression of cbnABCD positively in the presence of either 3-chlorobenzoate or benzoate, which are catabolized via 3-chlorocatechol and catechol, respectively. In vitro transcription assays confirmed that 2-chloro-cis,cis-muconate (2-CM) and cis, cis-muconate (CCM), intermediate products from 3-chlorocatechol and catechol, respectively, were inducers of this operon. This inducer-recognizing specificity is different from those of the homologous catechol (catBCA) and chlorocatechol (clcABD) operons of Pseudomonas putida, in which only the intermediates of the regulated pathway, CCM for catBCA and 2-CM for clcABD, act as significant inducers. Specific binding of CbnR protein to the cbnA promoter region was demonstrated by gel shift and DNase I footprinting analysis. In the absence of inducer, a region of ca. 60 bp from position -20 to position -80 upstream of the cbnA transcriptional start point was protected from DNase I cleavage by CbnR, with a region of hypersensitivity to DNase I cleavage clustered at position -50. Circular permutation gel shift assays demonstrated that CbnR bent the cbnA promoter region to an angle of 78 degrees and that this angle was relaxed to 54 degrees upon the addition of inducer. While a similar relaxation of bending angles upon the addition of inducer molecules observed with the catBCA and clcABD promoters may indicate a conserved transcriptional activation mechanism of ortho-cleavage pathway genes, CbnR is unique in having a different specificity of inducer recognition and the extended footprint as opposed to the restricted footprint of CatR without CCM.
真养产碱菌(以前称为嗜碱产碱菌)NH9通过改良的邻位裂解途径降解3-氯苯甲酸。一个约5.7 kb的六基因簇负责氯儿茶酚的降解:cbnABCD操纵子编码降解酶(包括功能未知的orfX),以及反向转录的cbnR基因,该基因编码cbn操纵子的LysR型转录调节因子。cbnRAB orfXCD基因簇与降解1,2,4-三氯苯的假单胞菌属菌株P51的氯儿茶酚基因(tcbRCD orfXEF)几乎相同。转录融合研究表明,在3-氯苯甲酸或苯甲酸存在的情况下,cbnR分别通过3-氯儿茶酚和儿茶酚对cbnABCD的表达进行正向调节。体外转录分析证实,2-氯-顺,顺-粘康酸(2-CM)和顺,顺-粘康酸(CCM)分别是3-氯儿茶酚和儿茶酚的中间产物,是该操纵子的诱导物。这种诱导物识别特异性不同于恶臭假单胞菌的同源儿茶酚(catBCA)和氯儿茶酚(clcABD)操纵子,在后者中,只有受调节途径的中间产物,catBCA的CCM和clcABD的2-CM,作为重要的诱导物。凝胶迁移和DNase I足迹分析证明了CbnR蛋白与cbnA启动子区域的特异性结合。在没有诱导物的情况下,CbnR保护了cbnA转录起始点上游约60 bp的区域(从-20到-80位)不被DNase I切割,在-50位聚集了一个对DNase I切割高度敏感的区域。环状置换凝胶迁移分析表明,CbnR将cbnA启动子区域弯曲至78度角,加入诱导物后该角度松弛至54度。虽然在catBCA和clcABD启动子上观察到加入诱导物分子后弯曲角度有类似的松弛,这可能表明邻位裂解途径基因存在保守的转录激活机制,但CbnR的独特之处在于具有不同的诱导物识别特异性和扩展的足迹,而不是没有CCM时CatR的受限足迹。