Arthur N. Mason
University of Dundee
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Featured researches published by Arthur N. Mason.
Journal of Steroid Biochemistry | 1985
Robert W. Owen; Arthur N. Mason; Rodney F. Bilton
Abstract The bacterial degradation of β-sitosterol by Pseudomonas sp NCIB 10590 has been studied. Major biotransformation products included 24-ethylcholest-4-en-3-one, androsta-1,4-diene-3,17-dione, 3-oxochol-4-en-3-one-24-oic acid and 3-oxopregn-4-en-3-one-20-carboxylic acid. Minor products identified were 26-hydroxy-24-ethylcholest-4-en-3-one, androst-4-ene-3,17-dione, 3-oxo-24-ethylcholest-4-en-26-oic acid, 3-oxochola-1,4-dien-3-one-24-oic acid, 3-oxopregna-1,4-dien-3-one-20 carboxylic acid and 9α-hydroxyandrosta-1,4-diene-3,17-dione. Studies with selected inhibitors have enabled the elucidation of a comprehensive pathway of β-sitosterol degradation by bacteria.
Journal of Steroid Biochemistry | 1979
M.E. Tenneson; J.D. Baty; Rodney F. Bilton; Arthur N. Mason
Abstract The microbial degradation of hyodeoxycholic acid by Pseudomonas spp. N.C.I.B. 10590 has been studied. Two major products and one minor product have been isolated and identified as 6α-hydroxyan-drosta-1, 4-dien-3,17-dione, 6α-hydroxy-3-oxopregna-1,4-dien-20-carboxylic acid and androsta-1,4-dien-3, 6,17-trione respectively. Two other minor products were isolated and evidence is given for the following structures: 6α-hydroxyandrost-4-en-3,17-dione and 6α-hydroxy-3-oxopregn-4-en-20-carboxylic acid. A possible paathway of hyodeoxycholic acid degradation is suggested.
Journal of Steroid Biochemistry | 1979
M.E. Tenneson; J.D. Baty; R.F. Bilton; Arthur N. Mason
Abstract The microbial degradation of chenodeoxycholic acid by Pseudomonas spp. N.C.I.B. 10590 has been studied. Two major products have been isolated and identified as 7α-hydroxy-1,4-androstadiene-3,17-dione and 7α-hydroxy-3-oxo-1,4-pregnadiene-20-carboxylic acid. Two minor products were isolated and evidence is given for the following structures: 1,4,6-androstatriene-3,17-dione and 7α-hydroxy-3-oxo-4-pregnene-20-carboxylic acid. A possible pathway of chenodeoxycholic acid degradation is suggested.
Journal of The Chemical Society, Chemical Communications | 1974
Peter J. Barnes; J. David Baty; Rodney F. Bilton; Arthur N. Mason
Deoxycholic acid has been converted into 12ξ-hydroxyandrosta-1,4-diene-3,17-dione by Pseudomonas sp. NCIB 10590.
Biochemical Society Transactions | 1978
Robert W. Owen; Michael E. Tenneson; Rodney F. Bilton; Arthur N. Mason
Biochemical Society Transactions | 1977
Michael E. Tenneson; Robert W. Owen; Arthur N. Mason
Biochemical Society Transactions | 1978
Michael E. Tenneson; Rodney F. Bilton; Arthur N. Mason
Biochemical Society Transactions | 1984
Kathleen Fadden; Robert W. Owen; M. J. Hill; Eva Latymer; A. Graham Low; Arthur N. Mason
Biochemical Society Transactions | 1978
Michael E. Tenneson; Rodney F. Bilton; Arthur N. Mason
Biochemical Society Transactions | 1975
Peter J. Barnes; Rodney F. Bilton; Arthur N. Mason; Fresia Fernandez; M. J. Hill