Please use this identifier to cite or link to this item: http://gukir.inflibnet.ac.in:8080/jspui/handle/123456789/4756
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dc.contributor.authorNayak, AS
dc.contributor.authorVeeranagouda, Y
dc.contributor.authorLee, K
dc.contributor.authorKaregoudar, TB
dc.date.accessioned2020-06-12T15:04:48Z-
dc.date.available2020-06-12T15:04:48Z-
dc.date.issued2009
dc.identifier.citationBIODEGRADATION , Vol. 20 , 6 , p. 837 - 843en_US
dc.identifier.uri10.1007/s10532-009-9271-1
dc.identifier.urihttp://gukir.inflibnet.ac.in:8080/jspui/handle/123456789/4756-
dc.description.abstractStenotrophomonas sp. RMSK capable of degrading acenaphthylene as a sole source of carbon and energy was isolated from coal sample. Metabolites produced were analyzed and characterized by TLC, HPLC and mass spectrometry. Identification of naphthalene-1,8-dicarboxylic acid, 1-naphthoic acid, 1,2-dihydroxynaphthalene, salicylate and detection of key enzymes namely 1,2-dihydroxynaphthalene dioxygenase, salicylaldehyde dehydrogenase and catechol-1,2-dioxygenase in the cell free extract suggest that acenaphthylene metabolized via 1,2-dihydroxynaphthalene, salicylate and catechol. The terminal metabolite, catechol was then metabolized by catechol-1,2-dioxygenase to cis,cis-muconic acid, ultimately forming TCA cycle intermediates. Based on these studies, the proposed metabolic pathway in strain RMSK is, acenaphthylene -> naphthalene-1,8-dicarboxylic acid -> 1-naphthoic acid -> 1,2-dihydroxynaphthalene -> salicylic acid -> catechol -> cis,cis-muconic acid.en_US
dc.publisherSPRINGER
dc.subjectAcenaphthylene
dc.subjectStenotrophomonas
dc.subject1,2-Dihydroxynaphthalene
dc.subjectBiodegradation
dc.subjectCatechol-1,2-dioxygenase
dc.titleMetabolism of acenaphthylene via 1,2-dihydroxynaphthalene and catechol by Stenotrophomonas sp RMSKen_US
dc.typeArticle
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