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Function and molecular ecology significance of two catechol-degrading gene clusters in Pseudomonas putida ND6.
Journal of Microbiology and Biotechnology ( IF 2.8 ) Pub Date : 2020-12-11 , DOI: 10.4014/jmb.2009.09026
Sanyuan Shi 1 , Liu Yang 1 , Chen Yang 1 , Shanshan Li 2 , Hong Zhao 3 , Lu Ren 1 , Xiaokang Wang 1 , Fuping Lu 1 , Ying Li 4 , Huabing Zhao 1
Affiliation  

Many bacteria metabolize aromatic compounds via catechol as a catabolic intermediate, and possess multiple genes or clusters encoding catechol-cleavage enzymes. The presence of multiple isozyme-encoding genes is a widespread phenomenon that seems to give the carrying strains a selective advantage in the natural environment over those with only a single copy. In the naphthalene-degrading strain Pseudomonas putida ND6, catechol can be converted into intermediates of the tricarboxylic acid cycle via either ortho- or meta-cleavage pathway. In this study, we demonstrated that the catechol ortho-cleavage pathway genes (catBICIAI and catBIICIIAII) on the chromosome play an important role. The catI and catII operons are co-transcribed, whereas catAI and catAII are under independent transcriptional regulation. We examined the binding of regulatory proteins to promoters. Inthe presence of cis-cis-muconate, a well-studied inducer of the cat gene cluster, CatRI and CatRII occupy an additional downstream site, designated as the activation binding site. Notably, CatRI binds to both the catI and catII promoters with high affinity, while CatRII binds weakly. This is likely caused by a T to G mutation in the G/T-N11-A motif. Specifically, we found that CatRI and CatRII regulate catBICIAI and catBIICIIAII in a cooperative manner, which provides new insights into naphthalene degradation.

中文翻译:

恶臭假单胞菌 ND6 中两个儿茶酚降解基因簇的功能和分子生态学意义。

许多细菌通过儿茶酚作为分解代谢中间体代谢芳香族化合物,并拥有编码儿茶酚裂解酶的多个基因或簇。多个同工酶编码基因的存在是一种普遍现象,与只有一个拷贝的菌株相比,携带菌株似乎在自然环境中具有选择性优势。在萘降解菌株Pseudomonas putida ND6 中,儿茶酚可以通过邻位或间位裂解途径转化为三羧酸循环的中间体。在这项研究中,我们证明了儿茶酚邻位裂解途径基因 ( catB I C I A IcatB IIC II A II )对染色体起着重要的作用。cat Icat II操纵子是共转录的,而 catAI 和 catAII 处于独立的转录调控之下。我们检查了调节蛋白与启动子的结合。在顺式-顺式-粘康酸盐(一种经过充分研究的 cat 基因簇诱导剂)存在的情况下,CatR I和 CatR II占据了一个额外的下游位点,指定为激活结合位点。值得注意的是,CatR I以高亲和力结合cat Icat II启动子,而 CatR II弱结合。这可能是由 G/TN 11 -A 基序中的 T 到 G 突变引起的。具体来说,我们发现 CatR I和 CatR II以合作的方式调节catB I C I A IcatB II C II A II,这为萘降解提供了新的见解。
更新日期:2020-12-18
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