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通过属间杂交构建一株利用3-氯联苯的重组体。

Construction of a 3-chlorobiphenyl-utilizing recombinant from an intergeneric mating.

作者信息

Adams R H, Huang C M, Higson F K, Brenner V, Focht D D

机构信息

Department of Soil and Environmental Sciences, University of California, Riverside 92521.

出版信息

Appl Environ Microbiol. 1992 Feb;58(2):647-54. doi: 10.1128/aem.58.2.647-654.1992.

Abstract

Recombinant Pseudomonas sp. strain CB15, which grows on 3-chlorobiphenyl (3CB), was constructed from Pseudomonas sp. strain HF1, which grows on 3-chlorobenzoate, and from Acinetobacter sp. strain P6, which grows on biphenyl, by using a continuous amalgamated culture apparatus. DNA from strains CB15 and HF1 hybridized very strongly to each other, while hybridization between both parental strains, HF1 and P6, was negligible. However, DNA from the recombinant CB15 hybridized moderately to strongly with three specific fragments of parental strain P6. Strains HF1 and P6 did not grow on 3CB, but recombinant strain CB15 mineralized this compound and released inorganic chloride. When growing on 3CB, strain CB15 accumulated brown products, one of which was identified as 3-chloro-5-(2'-hydroxy-3'-chlorophenyl)-1,2-benzoquinone by mass spectrometry. Emulsification and mechanical fragmentation greatly increased the rate of 3CB mineralization by strain CB15. At least three methods of inhibition from catecholic intermediates may account for slow growth on 3CB. The meta fission of 2,3-dihydroxybiphenyl (the nonchlorinated analog of the metabolic intermediate 3-chloro-2',3'-dihydroxybiphenyl) was affected by substrate inhibition (Vmax = 359 nmol.min-1.mg-1, Km = 114 microM, Kss [the inhibition constant] = 951 microM) and was also inhibited by 3-chlorocatechol. The ortho fission of 3-chlorocatechol, a degradation product, followed Michaelis-Menten kinetics (Vmax = 365 nmol.min-1.mg-1, Km = 1 microM), but the addition of 2,3-dihydroxybiphenyl inhibited the reaction (Ki = 0.87 microM).(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

利用连续合并培养装置,从能在3 - 氯苯甲酸上生长的假单胞菌属菌株HF1和能在联苯上生长的不动杆菌属菌株P6构建了能在3 - 氯联苯(3CB)上生长的重组假单胞菌属菌株CB15。菌株CB15和HF1的DNA彼此强烈杂交,而亲本菌株HF1和P6之间的杂交可忽略不计。然而,重组CB15的DNA与亲本菌株P6的三个特定片段中度至强烈杂交。菌株HF1和P6不能在3CB上生长,但重组菌株CB15使该化合物矿化并释放出无机氯。当在3CB上生长时,菌株CB15积累棕色产物,其中之一通过质谱鉴定为3 - 氯 - 5 -(2'-羟基 - 3'-氯苯基)-1,2 - 苯醌。乳化和机械破碎极大地提高了菌株CB15对3CB的矿化速率。来自儿茶酚中间体的至少三种抑制方法可能导致在3CB上生长缓慢。2,3 - 二羟基联苯(代谢中间体3 - 氯 - 2',3'-二羟基联苯的非氯化类似物)的间位裂解受底物抑制(Vmax = 359 nmol·min-1·mg-1,Km = 114 μM,Kss[抑制常数] = 951 μM),并且也受到3 - 氯儿茶酚的抑制。降解产物3 -氯儿茶酚的邻位裂解遵循米氏动力学(Vmax = 365 nmol·min-1·mg-1,Km = 1 μM),但添加2,3 - 二羟基联苯会抑制该反应(Ki = 0.87 μM)。(摘要截短于250字)

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/58ac/195297/5d73afa65e6d/aem00043-0226-a.jpg

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