Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/5633
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dc.contributor.authorKadam, T A-
dc.contributor.authorGangawane, L V-
dc.date.accessioned2009-07-30T06:03:13Z-
dc.date.available2009-07-30T06:03:13Z-
dc.date.issued2005-01-
dc.identifier.issn0975-0967 (Online); 0972-5849 (Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/5633-
dc.description153-155en_US
dc.description.abstract Of 44 Azotobacter isolates from the soils of Maharashtra, 29 belonged to A. chroococcum and other were A. vinelandii. All A. chroococcum isolates were efficient in N fixation when tested by acetylene reduction test and also in cotton cv NHH-44. However, they showed variation to phorate tolerance. The maximum tolerance (150 g/ml) was shown by ACI-17, ACI-18 and ACI-28 isolates. These isolates also showed maximum phorate degradation. TLC and HPLC studies indicated the presence of O,O-diethyl S-{(ethyl sulphonyl) methyl} phosphorothioate, O,O-diethyl S-{(ethyl sulphinyl) methyl} phosphorothioate and diethyl phosphoric acid as degradation products. Plasmid analysis indicated that the genes for phorate degradation might be located on the main chromosome and not on the plasmid. en_US
dc.language.isoen_USen_US
dc.publisherCSIRen_US
dc.relation.ispartofseriesInt. Cl.7 A 01 N 63/02en_US
dc.sourceIJBT Vol.4(1) [January 2005]en_US
dc.subjectAzotobacteren_US
dc.subjectN fixationen_US
dc.subjectphorateen_US
dc.subjecttoleranceen_US
dc.titleDegradation of phorate by Azotobacter isolatesen_US
dc.typeArticleen_US
Appears in Collections:IJBT Vol.04(1) [January 2005]

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