Literature DB >> 26216240

The biodegradation vs. biotransformation of fluorosubstituted aromatics.

Martina Kiel1, Karl-Heinrich Engesser.   

Abstract

Fluoroaromatics are widely and--in recent years--increasingly used as agrochemicals, starting materials for chemical syntheses and especially pharmaceuticals. This originates from the special properties the carbon-fluorine bond is imposing on organic molecules. Hence, fluoro-substituted compounds more and more are considered to be important potential environmental contaminants. On the other hand, the microbial potentials for their transformation and mineralization have received less attention in comparison to other haloaromatics. Due to the high electronegativity of the fluorine atom, its small size, and the extraordinary strength of the C-F bond, enzymes and mechanisms known to facilitate the degradation of chloro- or bromoarenes are not necessarily equally active with fluoroaromatics. Here, we review the literature on the microbial degradation of ring and side-chain fluorinated aromatic compounds under aerobic and anaerobic conditions, with particular emphasis being placed on the mechanisms of defluorination reactions.

Entities:  

Mesh:

Substances:

Year:  2015        PMID: 26216240     DOI: 10.1007/s00253-015-6817-5

Source DB:  PubMed          Journal:  Appl Microbiol Biotechnol        ISSN: 0175-7598            Impact factor:   4.813


  14 in total

1.  Aerobic degradation of 4-fluoroaniline and 2,4-difluoroaniline: performance and microbial community in response to the inocula.

Authors:  Zhi-Qing Zhao; Xiao-Meng Wei; Xiao-Li Shen; Ghulam Abbas; Rui Fan; Yi Jin
Journal:  Biodegradation       Date:  2021-01-11       Impact factor: 3.909

2.  Bacterial degradation of the anti-depressant drug fluoxetine produces trifluoroacetic acid and fluoride ion.

Authors:  Mohd Faheem Khan; Cormac D Murphy
Journal:  Appl Microbiol Biotechnol       Date:  2021-11-10       Impact factor: 4.813

3.  Biodegradation of 3-Chloronitrobenzene and 3-Bromonitrobenzene by Diaphorobacter sp. Strain JS3051.

Authors:  Zhi-Jing Xu; Jim C Spain; Ning-Yi Zhou; Tao Li
Journal:  Appl Environ Microbiol       Date:  2022-03-28       Impact factor: 5.005

4.  Microwell Fluoride Screen for Chemical, Enzymatic, and Cellular Reactions Reveals Latent Microbial Defluorination Capacity for -CF3 Groups.

Authors:  Madison D Bygd; Kelly G Aukema; Jack E Richman; Lawrence P Wackett
Journal:  Appl Environ Microbiol       Date:  2022-04-18       Impact factor: 5.005

Review 5.  Carbon-fluorine bond cleavage mediated by metalloenzymes.

Authors:  Yifan Wang; Aimin Liu
Journal:  Chem Soc Rev       Date:  2020-06-08       Impact factor: 54.564

6.  Promiscuous Defluorinating Enoyl-CoA Hydratases/Hydrolases Allow for Complete Anaerobic Degradation of 2-Fluorobenzoate.

Authors:  Oliver Tiedt; Mario Mergelsberg; Wolfgang Eisenreich; Matthias Boll
Journal:  Front Microbiol       Date:  2017-12-21       Impact factor: 5.640

7.  Combinatorial pathway balancing provides biosynthetic access to 2-fluoro-cis,cis-muconate in engineered Pseudomonas putida.

Authors:  Nicolas T Wirth; Pablo I Nikel
Journal:  Chem Catal       Date:  2021-11-18

8.  19F-centred NMR analysis of mono-fluorinated compounds.

Authors:  Alan J R Smith; Richard York; Dušan Uhrín; Nicholle G A Bell
Journal:  RSC Adv       Date:  2022-03-30       Impact factor: 3.361

9.  ATP-Dependent C-F Bond Cleavage Allows the Complete Degradation of 4-Fluoroaromatics without Oxygen.

Authors:  Oliver Tiedt; Mario Mergelsberg; Kerstin Boll; Michael Müller; Lorenz Adrian; Nico Jehmlich; Martin von Bergen; Matthias Boll
Journal:  mBio       Date:  2016-08-09       Impact factor: 7.867

10.  The ever-expanding limits of enzyme catalysis and biodegradation: polyaromatic, polychlorinated, polyfluorinated, and polymeric compounds.

Authors:  Lawrence P Wackett; Serina L Robinson
Journal:  Biochem J       Date:  2020-08-14       Impact factor: 3.857

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.