1. IR @ Gulbarga University
  2. Faculty Publications
  3. 1. Journal Articles
Please use this identifier to cite or link to this item: http://gukir.inflibnet.ac.in:8080/jspui/handle/123456789/4306
Full metadata record
DC FieldValueLanguage
dc.contributor.authorMonisha, TR
dc.contributor.authorIsmailsab, M
dc.contributor.authorMasarbo, R
dc.contributor.authorNayak, AS
dc.contributor.authorKaregoudar, TB
dc.date.accessioned2020-06-12T15:03:01Z-
dc.date.available2020-06-12T15:03:01Z-
dc.date.issued2018
dc.identifier.citation3 BIOTECH , Vol. 8 , 8 , p. -en_US
dc.identifier.uri10.1007/s13205-018-1390-0
dc.identifier.urihttp://gukir.inflibnet.ac.in:8080/jspui/handle/123456789/4306-
dc.description.abstractA bacterium Stenotrophomonas sp. TRMK2 capable of utilizing cinnamic acid was isolated from agro-industrial waste by enrichment culture technique. This strain completely utilizes 5 mM cinnamic acid within 18 h of incubation. The different metabolites formed during the degradation of cinnamic acid were characterized by GC-HRMS. The involvement of various enzymes, namely cinnamate reductase, 3-phenylpropionic acid hydroxylase, p-hydroxybenzoic acid hydroxylase and protocatechuate 3,4-dioxygenase in cinnamic acid degradation was demonstrated. A catabolic pathway for cinnamic acid in Stenotrophomonas sp. TRMK2 is as follows: Cinnamic acid; 3-Phenylpropionic acid; 3-(4-Hydroxyphenyl) propionic acid; 4-Hydroxy benzoic acid and Protocatechuic acid. Further, this strain is capable of utilizing various phenolic compounds.en_US
dc.publisherSPRINGER HEIDELBERG
dc.subjectBiodegradation
dc.subjectEnzymes
dc.subjectMetabolism
dc.subjectPollutants
dc.subjectWaste
dc.titleDegradation of cinnamic acid by a newly isolated bacterium Stenotrophomonas sp TRMK2en_US
dc.typeArticle
Appears in Collections:1. Journal Articles

Files in This Item:
There are no files associated with this item.
Show simple item record


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.