ArticleCurrent microbiology2018
Biodegradation of Pendimethalin by Paracoccus sp. P13.
Article in Current microbiology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
7 citing papers in PubMed, 29 citations in OpenAlex.
- Brevibacillus soli sp. nov., a Siderophore and IAA-Producing Strain Isolated from Soil.Current microbiology · 2026Article
- Biodegradation mechanism of butralin by a newly isolatedRSC advances · 2025Article
- Terrimonas alba sp. nov., an Ochratoxin A-Degrading Strain Isolated from Lakeside Soil.Current microbiology · 2025Article
- Paenibacillus mesotrionivorans sp. nov., a Mesotrione-Degrading Strain Isolated from Soil.Current microbiology · 2025Article
- Xinfangfangia pollutisoli sp. nov., Isolated from Clopyralid-Contaminated Soil.Current microbiology · 2022Article
- Comprehensive characterization of stress tolerant bacteria with plant growth-promoting potential isolated from glyphosate-treated environment.World journal of microbiology & biotechnology · 2021Article
- Degradation of pendimethalin by the yeast YC2 and determination of its two main metabolites.RSC advances · 2018Article
Corrections and comments
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Authors and funding
5 authors at 3 institutions in 1 country.
Funding
Abstract
In this study, a bacterial strain P13 capable of degrading pendimethalin was isolated from the soil of a fruit garden. Based on observed cellular morphology and physiology characteristics and a phylogenetic analysis of 16S rRNA gene sequences, strain P13 was identified as a member of the genus Paracoccus. Strain P13 grew on pendimethalin as the sole carbon source, and could degrade 100 mg/L pendimethalin within 2 days and 200 mg/L pendimethalin within 5 days. Pendimethalin degradation was proposed to be initiated by oxidation ring cleavage to yield 1,3-dinitro-2-(pentan-3-ylamino)butane-1,4-diol, an alkane organic compound that was identified by ultra-high performance liquid chromatography coupled to tandem mass spectrometry (UHPLC-MS/MS), which then underwent a series of enzymatic reactions to produce CO
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Registered trials
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