A new paradigm for biohydroxylation by Beauveria bassiana ATCC 7159
摘要:
The biohydroxylation of a series of amides and related amino, keto and hydrocarbon substrates by the fungal biocatalyst Beauveria bassiana ATCC 7159 has been examined. The product distributions, together with data obtained from selective inhibition experiments using the cyt.P-450 inhibitors isosafrole, 1-aminobenzotriazole and phenylacetylene, suggest that B. bassiana contains a range of hydroxylase enzymes with different substrate specificities. A paradigm is presented for the interpretation of the results of microbial hydroxylation and for the application of existing active site models for B. bassiana. (C) 1999 Elsevier Science Ltd. All rights reserved.
A new paradigm for biohydroxylation by Beauveria bassiana ATCC 7159
摘要:
The biohydroxylation of a series of amides and related amino, keto and hydrocarbon substrates by the fungal biocatalyst Beauveria bassiana ATCC 7159 has been examined. The product distributions, together with data obtained from selective inhibition experiments using the cyt.P-450 inhibitors isosafrole, 1-aminobenzotriazole and phenylacetylene, suggest that B. bassiana contains a range of hydroxylase enzymes with different substrate specificities. A paradigm is presented for the interpretation of the results of microbial hydroxylation and for the application of existing active site models for B. bassiana. (C) 1999 Elsevier Science Ltd. All rights reserved.
HICKS T. A.; SMITH C. E.; WILLIAMSON W. R. N.; DAY E. H., J. MED. CHEM., 1979, 22, NO 12, 1460-1464
作者:HICKS T. A.、 SMITH C. E.、 WILLIAMSON W. R. N.、 DAY E. H.
DOI:——
日期:——
A new paradigm for biohydroxylation by Beauveria bassiana ATCC 7159
作者:Herbert L Holland、Terence A Morris、Phillip J Nava、Mirjana Zabic
DOI:10.1016/s0040-4020(99)00393-2
日期:1999.6
The biohydroxylation of a series of amides and related amino, keto and hydrocarbon substrates by the fungal biocatalyst Beauveria bassiana ATCC 7159 has been examined. The product distributions, together with data obtained from selective inhibition experiments using the cyt.P-450 inhibitors isosafrole, 1-aminobenzotriazole and phenylacetylene, suggest that B. bassiana contains a range of hydroxylase enzymes with different substrate specificities. A paradigm is presented for the interpretation of the results of microbial hydroxylation and for the application of existing active site models for B. bassiana. (C) 1999 Elsevier Science Ltd. All rights reserved.