Weightman A J, Weightman A L, Slater J H
Appl Environ Microbiol. 1985 Jun;49(6):1494-501. doi: 10.1128/aem.49.6.1494-1501.1985.
Mutant strains of Pseudomonas putida PP3 capable of utilizing monochloroacetate (MCA) and dichloroacetate (DCA) as the sole sources of carbon and energy were isolated from chemostat cultures. The mutants differed from the parent strain in that they could grow on products of MCA and DCA dehalogenation (catalyzed by inducible dehalogenases I and II) and were resistant to growth inhibition by the two substrates. The growth inhibition of strain PP3 by MCA, DCA, and other halogenated alkanoic acids was studied. Sensitivity to dehalogenase substrates was related to the expression of the dehalogenase genes. For example, mutants producing elevated levels of one or both of the dehalogenases were sensitive to 2-monochloropropionate and 2-monochlorobutanoate at concentrations which did not affect the growth of strain PP3. P. putida PP1, the parent of strain PP3, was resistant to the inhibitory effects of MCA and DCA. Spontaneous mutants of strain PP3, also resistant to MCA and DCA, were selected at high frequency, and four different classes of these strains were distinguished on the basis of dehalogenase phenotype. All dehalogenase-producing mutants were inducible; no constitutive mutant has yet been isolated. Most of the resistant mutants examined did not produce one or both of the dehalogenase, and over half of those tested failed to revert back to the parental (strain PP3) phenotype, indicating that the observed mutations involved high-frequency deletion of DNA base sequences affecting expression of genes encoding dehalogenases and associated permease(s).
从恒化器培养物中分离出了恶臭假单胞菌PP3的突变菌株,这些菌株能够利用一氯乙酸(MCA)和二氯乙酸(DCA)作为唯一的碳源和能源。这些突变体与亲本菌株的不同之处在于,它们能够利用MCA和DCA脱卤产物(由诱导型脱卤酶I和II催化)生长,并且对这两种底物的生长抑制具有抗性。研究了MCA、DCA和其他卤代链烷酸对菌株PP3的生长抑制作用。对脱卤酶底物的敏感性与脱卤酶基因的表达有关。例如,产生一种或两种脱卤酶水平升高的突变体对2-一氯丙酸和2-一氯丁酸敏感,而这些浓度对菌株PP3的生长没有影响。PP3菌株的亲本恶臭假单胞菌PP1对MCA和DCA的抑制作用具有抗性。以高频率筛选出了PP3菌株的自发突变体,它们也对MCA和DCA具有抗性,并根据脱卤酶表型区分出了四类不同的菌株。所有产生脱卤酶的突变体都是可诱导的;尚未分离出组成型突变体。所检测的大多数抗性突变体不产生一种或两种脱卤酶,并且超过一半的测试突变体未能回复到亲本(PP3菌株)表型,这表明观察到的突变涉及影响编码脱卤酶和相关通透酶基因表达的DNA碱基序列的高频缺失。