Publications by authors named "Jiguo Qiu"

3,5-Dichloroaniline (3,5-DCA) is extensively used in synthesizing dicarboximide fungicides, medical compounds and dyes. Due to its widespread use in agriculture and industry, 3,5-DCA is often detected in groundwater, wastewater, sediments and soil, posing great risk to animals and humans. However, the genes and enzymes involved in 3,5-DCA degradation remain unidentified.

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  • Microbial ammonia oxidation is crucial for nitrogen cycling in various environments, but the specific mechanisms involved remain largely unclear.
  • Dirammox is a new process where ammonia is directly converted to nitrogen gas through hydroxylamine, bypassing nitrite and nitrate, and involves specific genes in Alcaligenes species.
  • The review covers the discovery of dirammox, its genetic and biochemical aspects, ecological implications, and suggests future research directions in this area.
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3,6-Dichlorosalicylic acid (3,6-DCSA) is the demethylation metabolite of herbicide 3,6-dichloro-2-methoxy benzoic acid (dicamba). Previous studies have shown that anaerobic sludge further transformed 3,6-DCSA through decarboxylation and dechlorination. However, the anaerobe, enzyme, and gene involved in the anaerobic degradation of 3,6-DCSA are still unknown.

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Dipicolinic acid is an essential component of bacterial spores for stress resistance, which is released into the environment after spore germination. In a previous study, a dip gene cluster was found to be responsible for the catabolism of dipicolinic acid in Alcaligenes faecalis JQ135. However, the transcriptional regulatory mechanism remains unclear.

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  • Isoprocarb (IPC) is a type of insecticide that can harm the environment and non-target organisms, but its breakdown process hasn't been studied until now.
  • Researchers isolated a new strain called D-6 from the Rhodococcus genus, which can degrade IPC, and identified a unique enzyme, IpcH, responsible for breaking down IPC into a less harmful compound, 2-isopropylphenol (IPP).
  • The study highlights IpcH's effectiveness against various carbamate insecticides and suggests that strain D-6 could be useful for cleaning up IPC-contaminated environments by reducing its toxicity.
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Cotinine, the primary metabolite of nicotine in the human body, is an emerging pollutant in aquatic environments. It causes environmental problems and is harmful to the health of humans and other mammals; however, the mechanisms of its biodegradation have been elucidated incompletely. In this study, a novel Gram-negative strain that could degrade and utilize cotinine as a sole carbon source was isolated from municipal wastewater samples, and its cotinine degradation characteristics and kinetics were determined.

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A Gram-staining-positive actinomycete named YZH12 was isolated from the sediment of the Yangtze River in Nanjing, Jiangsu province, China. Cells were aerobic, non-spore forming, non-motile, short rod (0.4-0.

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A Gram-stain-negative bacterium, designated LG-4, was isolated from sediment of Qiantang River in Zhejiang Province, PR China. Cells were strictly aerobic, non-spore-forming, non-motile and short-rod-shaped (1.0-1.

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  • - This study builds on previous research showing that a specific gene cluster in *X9* strain helps degrade salicylate via a CoA-mediated pathway and introduces a new transcriptional regulator, CehR4, which works differently than other known regulators.
  • - CehR4 forms an operon with the gentisyl-CoA thioesterase gene, while two other important genes for salicylate metabolism form another operon, and their overlapping promoters regulate their transcription.
  • - The binding sites for CehR4 were identified, revealing how it controls the gene cluster involved in salicylate degradation, shedding light on its regulatory role and emphasizing the relevance of microbial degradation in reducing harmful aromatic compounds in
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Phenacetin, an antipyretic and analgesic drug, poses a serious health risk to both humans and aquatic organisms, which is of concern since this micropollutant is frequently detected in various aquatic environments. However, rare pure bacterial cultures have been reported to degrade phenacetin. Therefore, in this study, the novel phenacetin-degrading strain PNT-23 was isolated from municipal wastewater and identified as a sp.

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  • SulE is an esterase enzyme that detoxifies sulfonylurea herbicides, offering a method to eliminate these harmful substances from the environment and support the creation of herbicide-resistant crops.
  • Researchers determined the crystal structures of SulE and a mutant variant, P44R, finding that SulE forms a dimer with a binding pocket capable of accommodating large herbicide molecules while also featuring a unique lid loop for substrate binding.
  • The P44R mutation enhances the flexibility of the lid loop, allowing better positioning of the herbicide's heterocyclic ring and resulting in a significant increase in the enzyme’s activity, providing a foundation for future enhancements in enzyme engineering.
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Phenazine-1-carboxamide (PCN), a phenazine derivative, can cause toxicity risks to non target organisms. In this study, the Gram-positive bacteria Rhodococcus equi WH99 was found to have the ability to degrade PCN. PzcH, a novel amidase belonging to amidase signature (AS) family, responsible for hydrolyzing PCN to PCA was identified from strain WH99.

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In our previous study, the phenazine-1-carboxylic acid (PCA) 1,2-dioxygenase gene cluster ( cluster) in Sphingomonas histidinilytica DS-9 was identified to be responsible for the conversion of PCA to 1,2-dihydroxyphenazine (Ren Y, Zhang M, Gao S, Zhu Q, et al. 2022. Appl Environ Microbiol 88:e00543-22).

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2,5-Pyridinedicarboxylic acid (2,5-PDA), a natural N-heterocyclic compound and a substitute for production in plastics, was widely distributed in industrial wastewater. However, the biodegradation of 2,5-PDA has been rarely reported. In this study, strain YJ-5, which could utilize 2,5-PDA as the sole carbon source for growth was isolated from pesticide-contaminated soil.

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Microbial ammonia oxidation is vital to the nitrogen cycle. A biological process, called Dirammox (direct ammonia oxidation, NH →NH OH→N ), has been recently identified in Alcaligenes ammonioxydans and Alcaligenes faecalis. However, its transcriptional regulatory mechanism has not yet been fully elucidated.

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  • The study focuses on the degradation of the insecticide carbofuran by specific bacterial strains, particularly strain CFD-1 and a newly isolated strain CFD-2.
  • Key enzymes involved in breaking down carbofuran phenol were identified, including hydroxylase, epoxide hydrolase, and ring cleavage dioxygenase, which play critical roles in the degradation process.
  • The gene cluster responsible for the degradation is highly conserved among different Sphingomonad strains and is linked to horizontal gene transfer, highlighting the bacteria's evolutionary adaptation to metabolize carbofuran due to its extensive agricultural use over the past 50 years.
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  • Acetochlor is a chloroacetamide herbicide that contaminates anoxic environments, prompting a search for effective degradation methods.
  • A sulfate-reducing bacterium, SRB-5, was isolated and can degrade acetochlor via a unique anaerobic pathway that transforms it into various metabolites.
  • SRB-5 shows potential for environmental cleanup by effectively degrading acetochlor and related herbicides in industrial wastewater and paddy sludge.
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Quinolinic acid (QA) is an essential nitrogen-containing aromatic heterocyclic compounds in organisms and it also acts as an important intermediate in chemical industry, which has strong neurotoxicity and cytotoxicity. The wide range of sources and applications caused the release and accumulation of QA in the environment which might poses a hazard to ecosystems and human health. However, few research on the degradation of QA by microorganisms and toxicity of QA and its metabolites were reported.

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Strains Rhodococcus qingshengii djl-6 and Rhodococcus jialingiae djl-6-2 both harbour the typical carbendazim degradation pathway with the hydrolysis of carbendazim to 2-aminobenzimidazole (2-AB) as the initial step. However, the enzymes involved in this process are still unknown. In this study, the previous reported carbendazim hydrolase MheI was found in strain djl-6, but not in strain djl-6-2, then another carbendazim hydrolase CbmA was obtained by a four-step purification strategy from strain djl-6-2.

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Dipicolinic acid (DPA), an essential pyridine derivative biosynthesized in spores, constitutes a major proportion of global biomass carbon pool. Alcaligenes faecalis strain JQ135 could catabolize DPA through the "3HDPA (3-ydroxyiicolinic cid) pathway." However, the genes involved in this 3HDPA pathway are still unknown.

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Picolinic acid (PA) is a natural toxic pyridine derivative as well as an important intermediate used in the chemical industry. In a previous study, we identified a gene cluster, , that responsible for the catabolism of PA in Alcaligenes faecalis JQ135. However, the transcriptional regulation of the cluster remains known.

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Phenazines are an important class of secondary metabolites and are primarily named for their heterocyclic phenazine cores, including phenazine-1-carboxylic acid (PCA) and its derivatives, such as phenazine-1-carboxamide (PCN) and pyocyanin (PYO). Although several genes involved in the degradation of PCA and PYO have been reported so far, the genetic foundations of PCN degradation remain unknown. In this study, a PCN-degrading bacterial strain, Sphingomonas histidinilytica DS-9, was isolated.

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Quinoline is a typical nitrogen-heterocyclic compound with high toxicity and carcinogenicity which exists ubiquitously in industrial wastewater. In this study, a new quinoline-degrading bacterial strain sp. JH145 was isolated from oil-contaminated soil.

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Quinolinic acid (QA) is a pyridine derivative that can be found in many organisms and is widely used in the chemical industry. However, QA possesses excitotoxic properties. To date, the catabolism of QA mediated by microorganisms has rarely been reported.

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  • 5-Hydroxypicolinic acid (5HPA) is a natural compound that can be degraded by certain microbes, specifically Alcaligenes faecalis JQ135, but its transcription regulation mechanisms were unclear.
  • A study identified the promoter and transcription start site for the gene cluster responsible for 5HPA degradation, revealing that the transcription is negatively regulated by a TetR family regulator called HpaR.
  • HpaR binds to two partially complementary DNA sequences in the promoter, and the presence of 5HPA prevents HpaR from binding, which enhances the gene's transcription responsible for degrading 5HPA.
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