2022
DOI: 10.1016/j.jbc.2022.101871
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Characterization of a phylogenetically distinct extradiol dioxygenase involved in the bacterial catabolism of lignin-derived aromatic compounds

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Cited by 7 publications
(2 citation statements)
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“…This was supported by similar abundances in the Lake Reference samples, which were not enclosed, nor subjected to any hydrocarbon additions during the monitoring period. The source of these mechanisms is likely from the degradation of complex and ubiquitous aromatics-based compounds, namely lignin, humic acids, and other complex organic molecules derived from woody and herbaceous plant matter in the organic-rich shoreline (De Haan 1976 , Navas et al 2022 ). These complex plant-based organic molecules are substrates for catechol 2,3 and catechol 1,2 dioxygenases, and their potential activity would be expected in an organic rich wetland shore type (De Haan 1976 , Briganti et al 1997 , Szabó et al 2007 ).…”
Section: Discussionmentioning
confidence: 99%
“…This was supported by similar abundances in the Lake Reference samples, which were not enclosed, nor subjected to any hydrocarbon additions during the monitoring period. The source of these mechanisms is likely from the degradation of complex and ubiquitous aromatics-based compounds, namely lignin, humic acids, and other complex organic molecules derived from woody and herbaceous plant matter in the organic-rich shoreline (De Haan 1976 , Navas et al 2022 ). These complex plant-based organic molecules are substrates for catechol 2,3 and catechol 1,2 dioxygenases, and their potential activity would be expected in an organic rich wetland shore type (De Haan 1976 , Briganti et al 1997 , Szabó et al 2007 ).…”
Section: Discussionmentioning
confidence: 99%
“…Sphingomonas paucimobilis SYK-6 cracked the benzene ring of MGA through DesZ and LigAB, and the hydroxyl group was oxidized to carbonyl group, resulting in 4-carboxyl-2-hydroxy-6-methoxy-6-oxyhexa-2, 4-dioleate (CHMOD) [ 105 ]. In Pseudomonas sp.CF600, the meta-cleavage pathway of catechol was found, and catechol was transformed by catechol 2,3 dioxygenase (C23O) to produce 2-hydroxyl mucosal hemialdehyde [ 106 ]. In addition, a study found that in S. paucimobilis SYK-6, with a biphenyl compound 2,2′-dihydroxy-3,3′-dimethoxy-5,5′-dicarboxylic biphenyl (DDVA) as the substrate, four enzymes with different functions were involved in the initial steps to degrade biphenyls.…”
Section: Lignin-degrading Enzymementioning
confidence: 99%