Barbour M G, Bayly R C
J Bacteriol. 1981 Sep;147(3):844-50. doi: 10.1128/jb.147.3.844-850.1981.
Synthesis of enzymes of the 4-hydroxyphenylacetate meta-cleavage pathway was studied in Pseudomonas putida wild-type strain P23X1 (NCIB 9865) and mutant strains which had either structural or regulatory gene mutations. Induction studies with mutant strains each defective in an enzyme of the pathway showed that 4-hydroxyphenylacetate induced the hydroxylase and that 3,4-dihydroxyphenylacetate induced the 2,3-oxygenase, aldehyde dehydrogenase, isomerase, decarboxylase, and hydratase. This showed that the hydroxylase structural gene does not exist in an operon that contains any other structural gene of this meta pathway. Studies of mutant strains that synthesized constitutively the 2,3-oxygenase and subsequent enzymes suggested that the regulation of synthesis of these enzymes was coincident, and, in such strains, the hydroxylase was inducible only. Observations made with a putative polarity mutant that lacked 2,3-oxygenase activity suggested that the structural genes encoding this enzyme and subsequent enzymes of the pathway exist in the same operon. Studies of a regulatory mutant strain that was defective in the induction of the 2,3-oxygenase and subsequent enzymes suggest that the 2,3-oxygenase operon is under positive control.
在恶臭假单胞菌野生型菌株P23X1(NCIB 9865)以及具有结构或调控基因突变的突变菌株中,研究了4-羟基苯乙酸间位裂解途径中酶的合成。对该途径中每种酶均有缺陷的突变菌株进行诱导研究表明,4-羟基苯乙酸诱导了羟化酶,而3,4-二羟基苯乙酸诱导了2,3-加氧酶、醛脱氢酶、异构酶、脱羧酶和水合酶。这表明羟化酶结构基因不存在于包含该间位途径任何其他结构基因的操纵子中。对组成型合成2,3-加氧酶及后续酶的突变菌株的研究表明,这些酶的合成调控是一致的,并且在这类菌株中,羟化酶只是可诱导的。对缺乏2,3-加氧酶活性的假定极性突变体的观察表明,编码该酶及该途径后续酶的结构基因存在于同一个操纵子中。对在2,3-加氧酶及后续酶诱导方面有缺陷的调控突变菌株的研究表明,2,3-加氧酶操纵子受到正调控。