2007
DOI: 10.1016/j.molcatb.2006.09.001
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Rapid conversion of ferulic acid to 4-vinyl guaiacol and vanillin metabolites by Debaryomyces hansenii

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Cited by 73 publications
(62 citation statements)
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“…Karmakar et al (2000) reported the same metabolites for FA degradation by Bacillus coagulans BK07. When FA is degraded by some microorganisms, 4-vinyl guaiacol is the major product, as observed by Mathew et al (2007) and in this study. FA degradation products at certain concentrations, including 400 μM vanillic acid, are toxic to plants (Jung et al 2004).…”
Section: Discussionsupporting
confidence: 77%
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“…Karmakar et al (2000) reported the same metabolites for FA degradation by Bacillus coagulans BK07. When FA is degraded by some microorganisms, 4-vinyl guaiacol is the major product, as observed by Mathew et al (2007) and in this study. FA degradation products at certain concentrations, including 400 μM vanillic acid, are toxic to plants (Jung et al 2004).…”
Section: Discussionsupporting
confidence: 77%
“…To investigate the physiological properties of isolates, 100 ml M-9FA liquid medium was inoculated with 1 ml bacterial culture and cultured at 37°C with shaking at 160 rpm. At regular time intervals, growth of isolates was measured in terms of the optical density of culture solutions at 600 nm (Mathew et al 2007).…”
Section: Methodsmentioning
confidence: 99%
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“…This mixture was further subjected to cationic polymerization at a low temperature, to yield a mixed polymer consisting of VG and 4-hydroxystyrene in 97% isolated yield. The ratio of monomer units in the polymer was determined by 31 P-NMR and was in close agreement with the ratio of the applied mixture, indicating that the copolymerization of VG and 4-hydroxystyrene proceeded smoothly. SEC confirmed the existence of a polymer with an Mn of 10,543 and a polydispersity of 2.15.…”
Section: Preparation Of Polymers From Biomasssupporting
confidence: 55%
“…Preliminary investigations of the structure of the obtained polymers was performed by 31 P-NMR after derivatization with an excess of 2-chloro-4,4,5,5-tetramethyldioxaphospholane, following a literature procedure [ 47 ]. The spectrum of PVG showed one broad signal at 139.8 ppm, indicating that polymerization of VG proceeded through the expected vinyl mechanism and no additional cross linking between the phenol units had occurred.…”
Section: Polymerization Of Vg and Characterization Of Pvgmentioning
confidence: 99%