Chen Xueting, Ji Junbin, Zhao Leizhen, Qiu Jiguo, Dai Chen, Wang Weiwu, He Jian, Jiang Jiandong, Hong Qing, Yan Xin
Key Laboratory of Agricultural Environmental Microbiology, Ministry of Agriculture, College of Life Sciences, Nanjing Agricultural University, Nanjing, Jiangsu, People's Republic of China.
Laboratory Center of Life Sciences, College of Life Sciences, Nanjing Agricultural University, Nanjing, Jiangsu, People's Republic of China.
Appl Environ Microbiol. 2017 Aug 31;83(18). doi: 10.1128/AEM.00868-17. Print 2017 Sep 15.
Buprofezin is a widely used insect growth regulator whose residue has been frequently detected in the environment, posing a threat to aquatic organisms and nontarget insects. Microorganisms play an important role in the degradation of buprofezin in the natural environment. However, the relevant catabolic pathway has not been fully characterized, and the molecular mechanism of catabolism is still completely unknown. YL-1 can utilize buprofezin as a sole source of carbon and energy for growth. In this study, the upstream catabolic pathway in strain YL-1 was identified using tandem mass spectrometry. Buprofezin is composed of a benzene ring and a heterocyclic ring. The degradation is initiated by the dihydroxylation of the benzene ring and continues via dehydrogenation, aromatic ring cleavage, breaking of an amide bond, and the release of the heterocyclic ring 2--butylimino-3-isopropyl-1,3,5-thiadiazinan-4-one (2-BI). A buprofezin degradation-deficient mutant strain YL-0 was isolated. A comparative genomic analysis combined with gene deletion and complementation experiments revealed that the gene cluster is responsible for the upstream catabolic pathway of buprofezin. The cluster encodes a novel Rieske nonheme iron oxygenase (RHO) system that is responsible for the dihydroxylation of buprofezin at the benzene ring; is involved in dehydrogenation, and is in charge of benzene ring cleavage. Furthermore, the products of can also catalyze dihydroxylation, dehydrogenation, and aromatic ring cleavage of biphenyl, flavanone, flavone, and bifenthrin. In addition, a transcriptional study revealed that is organized in one transcriptional unit that is constitutively expressed in strain YL-1. There is an increasing concern about the residue and environmental fate of buprofezin. Microbial metabolism is an important mechanism responsible for the buprofezin degradation in the natural environment. However, the molecular mechanism and genetic determinants of microbial degradation of buprofezin have not been well identified. This work revealed that gene cluster is responsible for the upstream catabolic pathway of buprofezin in YL-1. The products of could also degrade bifenthrin, a widely used pyrethroid insecticide. These findings enhance our understanding of the microbial degradation mechanism of buprofezin and benefit the application of strain YL-1 and in the bioremediation of buprofezin contamination.
噻嗪酮是一种广泛使用的昆虫生长调节剂,其残留物在环境中经常被检测到,对水生生物和非靶标昆虫构成威胁。微生物在自然环境中噻嗪酮的降解过程中发挥着重要作用。然而,相关的分解代谢途径尚未完全明确,分解代谢的分子机制仍然完全未知。YL-1能够利用噻嗪酮作为唯一的碳源和能源进行生长。在本研究中,利用串联质谱法确定了菌株YL-1中的上游分解代谢途径。噻嗪酮由一个苯环和一个杂环组成。降解过程始于苯环的双羟基化,随后通过脱氢、芳环裂解、酰胺键断裂以及杂环2-丁基亚氨基-3-异丙基-1,3,5-噻二嗪-4-酮(2-BI)的释放而继续。分离得到了一株噻嗪酮降解缺陷型突变菌株YL-0。通过比较基因组分析结合基因缺失和互补实验表明,基因簇负责噻嗪酮的上游分解代谢途径。该基因簇编码一种新型的 Rieske 非血红素铁加氧酶(RHO)系统,负责噻嗪酮苯环的双羟基化;参与脱氢反应,负责芳环裂解。此外,该基因簇的产物还能催化联苯、黄烷酮、黄酮和联苯菊酯的双羟基化、脱氢和芳环裂解反应。此外,转录研究表明,该基因簇组织在一个转录单元中,在菌株YL-1中组成型表达。人们对噻嗪酮的残留和环境归宿越来越关注。微生物代谢是自然环境中噻嗪酮降解的重要机制。然而,噻嗪酮微生物降解的分子机制和遗传决定因素尚未得到很好的确定。这项工作表明,基因簇负责菌株YL-1中噻嗪酮的上游分解代谢途径。该基因簇的产物还能降解联苯菊酯,一种广泛使用的拟除虫菊酯类杀虫剂。这些发现加深了我们对噻嗪酮微生物降解机制的理解,并有利于菌株YL-1和该基因簇在噻嗪酮污染生物修复中的应用。