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脱卤脱硫杆菌JW/IU-DC1对取代邻氯苯酚的还原脱卤作用的特异性

Specificity of reductive dehalogenation of substituted ortho-chlorophenols by Desulfitobacterium dehalogenans JW/IU-DC1.

作者信息

Utkin I, Dalton D D, Wiegel J

机构信息

Department of Microbiology, University of Georgia, Athens 30602-2605.

出版信息

Appl Environ Microbiol. 1995 Jan;61(1):346-51. doi: 10.1128/aem.61.1.346-351.1995.

DOI:10.1128/aem.61.1.346-351.1995
PMID:7887614
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC167288/
Abstract

Resting cells of Desulfitobacterium dehalogenans JW/IU-DC1 growth with pyruvate and 3-chloro-4-hydroxyphenylacetate (3-Cl-4-OHPA) as the electron acceptor and inducer of dehalogenation reductively ortho-dehalogenate pentachlorophenol (PCP); tetrachlorophenols (TeCPs); the trichlorophenols 2,3,4-TCP, 2,3,6-TCP, and 2,4,6-TCP; the dichlorophenols 2,3-DCP, 2,4-DCP, and 2,6-DCP; 2,6-dichloro-4-R-phenols (2,6-DCl-4-RPs, where R is -H, -F, -Cl, -NO2, -CO2, or -COOCH3; 2-chloro-4-R-phenols (2-Cl-4-RPs, where R is -H, -F, -Cl, -Br, -NO2, -CO2-, -CH2CO2, or -COOCH3); and the bromophenols 2-BrP, 2,6-DBrP, and 2-Br-4ClP [corrected]. Monochlorophenols, the dichlorophenols 2,5-DCP, 3,4-DCP, and 3,5-DCP, the trichlorophenols 2,3,5-TCP, 2,4,5-TCP, and 3,4,5-TCP, and the fluorinated analog of 3-Cl-4-OHPA, 3-F-4-OHPA ("2-F-4-CH2CO2- P"), are not dehalogenated. A chlorine substituent in position 3 (meta), 4 (para), or 6 (second ortho) of the phenolic moiety facilitates ortho dehalogenation in position 2. Chlorine in the 5 (second meta) position has a negative effect on the dehalogenation rate or even prevents dechlorination in the 2 position. In general, 2,6-DCl-4-RPs are dechlorinated faster than the corresponding 2-Cl-4-RPs with the same substituent R in the 4 position. The highest dechlorination rate, however, was found for dechlorination of 2,3-DCP, with a maximal observed first-order rate constant of 19.4 h-1 g (dry weight) of biomass-1.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

脱卤脱硫杆菌JW/IU-DC1的静息细胞以丙酮酸和3-氯-4-羟基苯乙酸(3-Cl-4-OHPA)作为电子受体和脱卤诱导剂,可对五氯苯酚(PCP);四氯苯酚(TeCPs);三氯苯酚2,3,4-TCP、2,3,6-TCP和2,4,6-TCP;二氯苯酚2,3-DCP、2,4-DCP和2,6-DCP;2,6-二氯-4-R-苯酚(2,6-DCl-4-RPs,其中R为-H、-F、-Cl、-NO2、-CO2或-COOCH3);2-氯-4-R-苯酚(2-Cl-4-RPs,其中R为-H、-F、-Cl、-Br、-NO2、-CO2-、-CH2CO2或-COOCH3);以及溴苯酚2-BrP、2,6-DBrP和2-Br-4ClP进行还原性邻位脱卤。单氯苯酚、二氯苯酚2,5-DCP、3,4-DCP和3,5-DCP、三氯苯酚2,3,5-TCP、2,4,5-TCP和3,4,5-TCP以及3-Cl-4-OHPA的氟化类似物3-F-4-OHPA(“2-F-4-CH2CO2-P”)不会发生脱卤反应。酚基部分3位(间位)、4位(对位)或6位(第二个邻位)的氯取代基有助于2位的邻位脱卤。5位(第二个间位)的氯对脱卤速率有负面影响,甚至会阻止2位的脱氯反应。一般来说,2,6-DCl-4-RPs的脱氯速度比4位具有相同取代基R的相应2-Cl-4-RPs快。然而,2,3-DCP脱氯的最高脱氯速率被发现,观察到的最大一级速率常数为19.4 h-1 g(干重)生物量-1。(摘要截短于250字)

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