Peng_2023_J.Hazard.Mater_442_130071

Reference

Title : Citrobacter sp. Y3 harbouring novel gene HBCD-hd-1 mineralizes hexabromocyclododecane via new metabolic pathways according to multi-omics characterization - Peng_2023_J.Hazard.Mater_442_130071
Author(s) : Peng X , Li T , Zheng Q , Lu Y , He Y , Tang Y , Qiu R
Ref : J Hazard Mater , 442 :130071 , 2023
Abstract :

Hexabromocyclododecane (HBCD) is a typical persistent organic pollutant that is widely detected in the environment. Despite the significant efforts put into its mineralisation, there is still a lack of microorganism resources that can completely mineralise HBCD. Stable isotope analysis revealed that the Citrobacter sp. Y3 can use [(13)C]HBCD as its sole carbon source and degrade or even mineralise it into (13)CO(2), with a maximum conversion rate of 100% in approximately 14 days. Strain Y3 could completely mineralise HBCD, which it used as its only carbon source, and six debromination enzymes related to HBCD degradation were found in Y3, including haloalkane dehalogenase (DhaA), haloacid dehalogenase (HAD), etc. A functional gene named HBCD-hd-1, encoding a HAD, was found to be upregulated during HBCD degradation and heterologously expressed in Escherichia coli. Recombinant E. coli with the HBCD-hd-1 gene transformed the typical intermediate 4-bromobutyric acid to 4-hydroxybutanoic acid and showed excellent degradation performance on HBCD, accompanied by nearly 100% bromine (Br) ion generation. The expression of HBCD-hd-1 in Y3 rapidly accelerated the biodegradation of HBCD. With HBCD as its sole carbon source, strain Y3 could potentially degrade HBCD, especially in a low-nutrient environment.

PubMedSearch : Peng_2023_J.Hazard.Mater_442_130071
PubMedID: 36183513

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Citations formats

Peng X, Li T, Zheng Q, Lu Y, He Y, Tang Y, Qiu R (2023)
Citrobacter sp. Y3 harbouring novel gene HBCD-hd-1 mineralizes hexabromocyclododecane via new metabolic pathways according to multi-omics characterization
J Hazard Mater 442 :130071

Peng X, Li T, Zheng Q, Lu Y, He Y, Tang Y, Qiu R (2023)
J Hazard Mater 442 :130071