Ahmad D, Fraser J, Sylvestre M, Larose A, Khan A, Bergeron J, Juteau J M, Sondossi M
Institut National de la Recherche Scientifique, INRS-Santé, Université du Québec, Pointe-Claire, Québec, Canada.
Gene. 1995 Apr 14;156(1):69-74. doi: 10.1016/0378-1119(95)00073-f.
The nucleotide sequence of bphD, encoding 2-hydroxy-6-oxo-(phenyl/chlorophenyl)hexa-2,4-dienoic acid hydrolase involved in the biphenyl/polychlorinated biphenyl degradation pathway of Comamonas testosteroni strain B-356, was determined. Comparison of the deduced amino-acid sequence with published sequences led to the identification of a 'lipase box', containing a consensus pentapeptide sequence GlyXaaSerXaaGly. This suggested that the mechanism of action of this enzyme may involve an Asp-Ser-His catalytic triad similar to that of classical lipases and serine hydrolases. Further biochemical and genetic evidence for the active-site involvement of Ser112 was obtained by showing that a semipurified enzyme was inhibited by PMSF, a classic inhibitor of serine hydrolases, and by site-directed Ser112-->Ala mutagenesis.
测定了睾丸酮丛毛单胞菌菌株B - 356参与联苯/多氯联苯降解途径的2 - 羟基 - 6 - 氧代 -(苯基/氯苯基)己 - 2,4 - 二烯酸水解酶编码基因bphD的核苷酸序列。将推导的氨基酸序列与已发表序列进行比较,鉴定出一个“脂肪酶框”,其中包含一个共有五肽序列GlyXaaSerXaaGly。这表明该酶的作用机制可能涉及与经典脂肪酶和丝氨酸水解酶类似的天冬氨酸 - 丝氨酸 - 组氨酸催化三联体。通过显示半纯化酶被丝氨酸水解酶的经典抑制剂苯甲基磺酰氟(PMSF)抑制以及通过定点丝氨酸112→丙氨酸诱变,获得了丝氨酸112参与活性位点的进一步生化和遗传证据。