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萘降解丛毛单胞菌JB对二苯并呋喃和二苯并噻吩的共代谢降解

Cometabolic Degradation of Dibenzofuran and Dibenzothiophene by a Naphthalene-Degrading Comamonas sp. JB.

作者信息

Ji Xiangyu, Xu Jing, Ning Shuxiang, Li Nan, Tan Liang, Shi Shengnan

机构信息

School of Life Science, Liaoning Normal University, Dalian, 116081, China.

Liaoning Ocean and Fisheries Science Research Institute, Dalian, 116023, China.

出版信息

Curr Microbiol. 2017 Dec;74(12):1411-1416. doi: 10.1007/s00284-017-1334-7. Epub 2017 Aug 18.

Abstract

Comamonas sp. JB was used to investigate the cometabolic degradation of dibenzofuran (DBF) and dibenzothiophene (DBT) with naphthalene as the primary substrate. Dehydrogenase and ATPase activity of the growing system with the presence of DBF and DBT were decreased when compared to only naphthalene in the growing system, indicating that the presence of DBF and DBT inhibited the metabolic activity of strain JB. The pathways and enzymes involved in the cometabolic degradation were tested. Examination of metabolites elucidated that strain JB cometabolically degraded DBF to 1,2-dihydroxydibenzofuran, subsequently to 2-hydroxy-4-(3'-oxo-3'H-benzofuran-2'-yliden)but-2-enoic acid, and finally to catechol. Meanwhile, strain JB cometabolically degraded DBT to 1,2-dihydroxydibenzothiophene and subsequently to the ring cleavage product. A series of naphthalene-degrading enzymes including naphthalene dioxygenase, 1,2-dihydroxynaphthalene dioxygenase, salicylaldehyde dehydrogenase, salicylate hydroxylase, and catechol 2,3-oxygenase have been detected, confirming that naphthalene was the real inducer of expression the degradation enzymes and metabolic pathways were controlled by naphthalene-degrading enzymes.

摘要

以食酸菌属菌株JB为研究对象,考察了以萘为主要底物时,其对二苯并呋喃(DBF)和二苯并噻吩(DBT)的共代谢降解情况。与仅含萘的生长体系相比,含DBF和DBT的生长体系中脱氢酶和ATP酶的活性降低,这表明DBF和DBT的存在抑制了菌株JB的代谢活性。对共代谢降解涉及的途径和酶进行了测试。通过对代谢产物的检测表明,菌株JB将DBF共代谢降解为1,2 - 二羟基二苯并呋喃,随后降解为2 - 羟基 - 4 -(3'-氧代-3'H - 苯并呋喃-2'-亚基)丁-2-烯酸,最终降解为儿茶酚。同时,菌株JB将DBT共代谢降解为1,2 - 二羟基二苯并噻吩,随后降解为开环产物。检测到一系列萘降解酶,包括萘双加氧酶、1,2 - 二羟基萘双加氧酶、水杨醛脱氢酶、水杨酸羟化酶和儿茶酚2,3 - 加氧酶,证实萘是降解酶表达的真正诱导物,代谢途径由萘降解酶控制。

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