Ramos J L, Duque E, Rodríguez-Herva J J, Godoy P, Haïdour A, Reyes F, Fernández-Barrero A
Department of Organic Chemistry, University of Granada, 18012 Granada, Spain.
J Biol Chem. 1997 Feb 14;272(7):3887-90. doi: 10.1074/jbc.272.7.3887.
The development of tolerance in Pseudomonas putida DOT-T1 to toluene and related highly toxic compounds involves short- and long-term responses. The short-term response is based on an increase in the rigidity of the cell membrane by rapid transformation of the fatty acid cis-9,10-methylene hexadecanoic acid (C17:cyclopropane) to unsaturated 9-cis-hexadecenoic acid (C16:1,9 cis) and subsequent transformation to the trans isomer. The long-term response involves in addition to the changes in fatty acids, alterations in the level of the phospholipid polar head groups: cardiolipin increases and phosphatidylethanolamine decreases. The two alterations lead to increased cell membrane rigidity and should be regarded as physical mechanisms that prevent solvent penetrance. Biochemical mechanisms that decrease the concentration of toluene in the cell membrane also take place and involve: (i) a solvent exclusion system and (ii) metabolic removal of toluene via oxidation. Mutants unable to carry out cis --> trans isomerization of unsaturated lipids, that exhibit altered cell envelopes because of the lack of the OprL protein, or that are unable to exclude toluene from cell membranes are hypersensitive to toluene.
恶臭假单胞菌DOT-T1对甲苯及相关剧毒化合物耐受性的发展涉及短期和长期反应。短期反应基于细胞膜刚性的增加,这是通过脂肪酸顺式-9,10-亚甲基十六烷酸(C17:环丙烷)快速转化为不饱和9-顺式十六碳烯酸(C16:1,9顺式),随后再转化为反式异构体实现的。长期反应除了脂肪酸的变化外,还涉及磷脂极性头部基团水平的改变:心磷脂增加而磷脂酰乙醇胺减少。这两种改变导致细胞膜刚性增加,应被视为防止溶剂渗透的物理机制。降低细胞膜中甲苯浓度的生化机制也会发生,包括:(i)溶剂排斥系统和(ii)通过氧化对甲苯进行代谢清除。无法进行不饱和脂质顺式→反式异构化、因缺乏OprL蛋白而表现出细胞包膜改变或无法将甲苯从细胞膜中排除的突变体对甲苯高度敏感。