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产碱假单胞菌中通过龙胆酸途径降解间甲酚和2,5-二甲酚所使用的同功酶的证据。

Evidence for isofunctional enzymes used in m-cresol and 2,5-xylenol degradation via the gentisate pathway in Pseudomonas alcaligenes.

作者信息

Poh C L, Bayly R C

出版信息

J Bacteriol. 1980 Jul;143(1):59-69. doi: 10.1128/jb.143.1.59-69.1980.

Abstract

Study of the reaction sequence by which Pseudomonas alcaligenes (P25X1) and derived mutants degrade m-cresol, 2,5-xylenol, and their catabolites has provided indirect evidence for the existence of two or more isofunctional enzymes at three different steps. Maleylpyruvate hydrolase activity appears to reside in two different proteins with different specificity ranges, one of which (MPH1) is expressed constitutively; the other (MPH11) is strictly inducible. Two gentisate 1,2-dioxygenase activities were found, one of which is constitutively expressed and possesses a broader specificity range than the other, which is inducible. From oxidation studies with intact cells, there appear to be two activities responsible for the 6-hydroxylation of 3-hydroxybenzoate, and again a broadly specific activity is present regardless of growth conditions; the other is inducible by 3-hydroxybenzoate. Three other enzyme activities are also detected in uninduced cells, viz., xylenol methylhydroxylase, benzylalcohol dehydrogenase, and benzaldehyde dehydrogenase. All apparently possess broad specificity. Fumarylpyruvate hydrolase was also detected but only in cells grown with m-cresol, 3-hydroxybenzoate, or gentisate. Mutants, derived either spontaneously or after treatment with mitomycin C, are described, certain of which have lost the ability to grow with m-cresol and 2,5-xylenol and some of which have also lost the ability to form the constitutive xylenol methylhydroxylase, benzylalcohol dehydrogenase, benzaldehyde dehydrogenase, 3-hydroxybenzoate 6-hydroxylase, and gentisate 1,2-dioxygenase. Such mutants, however, retain ability to synthesize inducibly a second 3-hydroxybenzoate 6-hydroxylase and gentisate 1,2-dioxygenase, as well as maleylpyruvate hydrolase (MPH11) and fumarylpyruvate hydrolase; MPH1 was still synthesized. These findings suggest the presence of a plasmid for 2,5-xylenol degradation which codes for synthesis of early degradative enzymes. Other enzymes, such as the second 3-hydroxybenzoate 6-hydroxylase, gentisate 1,2-dioxygenase, maleylpyruvate hydrolase (MPH1 and MPH11), and fumarylpyruvate hydrolase, appear to be chromosomally encoded and, with the exception of MPH1, strictly inducible.

摘要

对产碱假单胞菌(P25X1)及其衍生突变体降解间甲酚、2,5-二甲酚及其分解代谢物的反应序列进行研究,为三个不同步骤中存在两种或更多种同功酶提供了间接证据。马来酰丙酮酸水解酶活性似乎存在于两种具有不同特异性范围的不同蛋白质中,其中一种(MPH1)组成型表达;另一种(MPH11)严格可诱导。发现了两种龙胆酸1,2-双加氧酶活性,其中一种组成型表达,且比另一种可诱导的具有更广泛的特异性范围。通过完整细胞的氧化研究,似乎有两种活性负责3-羟基苯甲酸的6-羟基化,并且无论生长条件如何,都存在一种广泛特异性的活性;另一种由3-羟基苯甲酸诱导。在未诱导的细胞中还检测到另外三种酶活性,即二甲酚甲基羟化酶、苄醇脱氢酶和苯甲醛脱氢酶。所有这些酶显然都具有广泛的特异性。富马酰丙酮酸水解酶也被检测到,但仅在以间甲酚、3-羟基苯甲酸或龙胆酸生长的细胞中。描述了自发产生或经丝裂霉素C处理后得到的突变体,其中某些突变体失去了以间甲酚和2,5-二甲酚生长的能力,一些突变体还失去了形成组成型二甲酚甲基羟化酶、苄醇脱氢酶、苯甲醛脱氢酶、3-羟基苯甲酸6-羟化酶和龙胆酸1,2-双加氧酶的能力。然而,这些突变体仍保留可诱导合成第二种3-羟基苯甲酸6-羟化酶和龙胆酸1,2-双加氧酶以及马来酰丙酮酸水解酶(MPH11)和富马酰丙酮酸水解酶的能力;MPH1仍可合成。这些发现表明存在一个编码早期降解酶合成的用于2,5-二甲酚降解的质粒。其他酶,如第二种3-羟基苯甲酸6-羟化酶、龙胆酸1,2-双加氧酶、马来酰丙酮酸水解酶(MPH1和MPH11)和富马酰丙酮酸水解酶,似乎是由染色体编码的,并且除MPH1外,严格可诱导。

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