Junker F, Ramos J L
Department of Plant Biochemistry and Molecular and Cellular Biology, Estacion Experimental del Zaidin, Consejo Superior de Investigaciones Cientificas, E-18008 Granada, Spain.
J Bacteriol. 1999 Sep;181(18):5693-700. doi: 10.1128/JB.181.18.5693-5700.1999.
Pseudomonas putida DOT-T1E is a solvent-resistant strain that is able to grow in the presence of high concentrations of toluene. We have cloned and sequenced the cti gene of this strain, which encodes the cis/trans isomerase, termed Cti, that catalyzes the cis-trans isomerization of esterified fatty acids in phospholipids, mainly cis-oleic acid (C(16:1,9)) and cis-vaccenic acid (C(18:1,11)), in response to solvents. To determine the importance of this cis/trans isomerase for solvent resistance a Cti-null mutant was generated and characterized. This mutant showed a longer lag phase when grown with toluene in the vapor phase; however, after the lag phase the growth rate of the mutant strain was similar to that of the wild type. The mutant also showed a significantly lower survival rate when shocked with 0.08% (vol/vol) toluene. In contrast to the wild-type strain, which grew in liquid culture medium at temperatures up to 38.5 degrees C, the Cti-null mutant strain grew significantly slower at temperatures above 37 degrees C. An in-frame fusion of the Cti protein with the periplasmic alkaline phosphatase suggests that this constitutively expressed enzyme is located in the periplasm. Primer extension studies confirmed the constitutive expression of Cti. Southern blot analysis of total DNA from various pseudomonads showed that the cti gene is present in all the tested P. putida strains, including non-solvent-resistant ones, and in some other Pseudomonas species.
恶臭假单胞菌DOT-T1E是一种耐溶剂菌株,能够在高浓度甲苯存在的情况下生长。我们已经克隆并测序了该菌株的cti基因,该基因编码顺/反异构酶,称为Cti,它催化磷脂中酯化脂肪酸的顺反异构化,主要是顺式油酸(C(16:1,9))和顺式vaccenic酸(C(18:1,11)),以响应溶剂。为了确定这种顺/反异构酶对耐溶剂性的重要性,构建并表征了一个Cti缺失突变体。该突变体在气相中用甲苯培养时显示出更长的延迟期;然而,在延迟期之后,突变菌株的生长速率与野生型相似。当用0.08%(体积/体积)甲苯冲击时,该突变体的存活率也显著降低。与在高达38.5摄氏度的液体培养基中生长的野生型菌株不同,Cti缺失突变体菌株在高于37摄氏度的温度下生长明显较慢。Cti蛋白与周质碱性磷酸酶的框内融合表明,这种组成型表达的酶位于周质中。引物延伸研究证实了Cti的组成型表达。对来自各种假单胞菌的总DNA进行的Southern印迹分析表明,cti基因存在于所有测试的恶臭假单胞菌菌株中,包括非耐溶剂菌株,以及一些其他假单胞菌属物种中。