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Isolation and Characterization of Toluene-Sensitive Mutants from the Toluene-Resistant Bacterium Pseudomonas putida GM73

机译:耐假细菌恶臭假单胞菌GM73中甲苯敏感突变体的分离与鉴定

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摘要

To understand the mechanism underlying toluene resistance of a toluene-tolerant bacterium, Pseudomonas putida GM73, we carried out Tn5 mutagenesis and isolated eight toluene-sensitive mutants. None of the mutants grew in the presence of 20% (vol/vol) toluene in growth medium but exhibited differential sensitivity to toluene. When wild-type cells were treated with toluene (1% [vol/vol]) for 5 min, about 2% of the cells could form colonies. In the mutants Ttg1, Ttg2, Ttg3, and Ttg8, the same treatment killed more than 99.9999% of cells (survival rate, <10−6). In Ttg4, Ttg5, Ttg6, and Ttg7, about 0.02% of cells formed colonies. We cloned the Tn5-inserted genes, and the DNA sequence flanking Tn5 was determined. From comparison with a sequence database, putative protein products encoded by ttg genes were identified as follows. Ttg1 and Ttg2 are ATP binding cassette (ABC) transporter homologs; Ttg3 is a periplasmic linker protein of a toluene efflux pump; both Ttg4 and Ttg7 are pyruvate dehydrogenase; Ttg5 is a dihydrolipoamide acetyltransferase; and Ttg7 is the negative regulator of the phosphate regulon. The sequences deduced from ttg8 did not show a significant similarity to any DNA or proteins in sequence databases. Characterization of these mutants and identification of mutant genes suggested that active efflux mechanism and efficient repair of damaged membranes were important in toluene resistance.
机译:为了了解耐甲苯细菌假单胞菌GM73的耐甲苯性的机制,我们进行了Tn5诱变并分离了八个对甲苯敏感的突变体。在生长培养基中存在20%(体积/体积)甲苯的情况下,没有一个突变体生长,但是对甲苯表现出不同的敏感性。当用甲苯(1%(体积/体积))处理野生型细胞5分钟时,约2%的细胞可以形成菌落。在Ttg1,Ttg2,Ttg3和Ttg8突变体中,相同的处理杀死了99.9999%以上的细胞(存活率,<10 -6 )。在Ttg4,Ttg5,Ttg6和Ttg7中,约0.02%的细胞形成菌落。我们克隆了插入Tn5的基因,并确定了Tn5侧翼的DNA序列。通过与序列数据库比较,鉴定出由ttg基因编码的推定蛋白质产物如下。 Ttg1和Ttg2是ATP结合盒(ABC)转运蛋白同源物; Ttg3是甲苯外排泵的周质连接蛋白。 Ttg4和Ttg7均为丙酮酸脱氢酶。 Ttg5是二氢脂酰胺乙酰转移酶; Ttg7是磷酸调节子的负调节剂。从ttg8推导的序列与序列数据库中的任何DNA或蛋白质均未显示出显着相似性。这些突变体的表征和突变基因的鉴定表明,主动外排机制和对受损膜的有效修复在甲苯抗性中很重要。

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