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Featured researches published by Arthur N. Mason.


Journal of Steroid Biochemistry | 1985

The degradation of β-sitosterol by pseudomonas sp. NCIB 10590 under aerobic conditions

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

The degradation of hyodeoxycholic acid by Pseudomonas spp. N.C.I.B. 10590

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

The degradation of chenodeoxycholic acid by Pseudomonas Spp. N.C.I.B. 10590.

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

Novel microbial transformation of deoxycholic acid

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

The degradation of cholesterol by Escherichia coli isolated from human faeces [proceedings].

Robert W. Owen; Michael E. Tenneson; Rodney F. Bilton; Arthur N. Mason


Biochemical Society Transactions | 1977

The anaerobic side-chain cleavage of bile acids by Escherichia coli isolated from human faeces [proceedings].

Michael E. Tenneson; Robert W. Owen; Arthur N. Mason


Biochemical Society Transactions | 1978

A scheme for the microbial degradation of lithocholic acid involving testosterone as an intermediate [proceedings].

Michael E. Tenneson; Rodney F. Bilton; Arthur N. Mason


Biochemical Society Transactions | 1984

Steroid degradation along the gastrointestinal tract: the use of the cannulated pig as a model system

Kathleen Fadden; Robert W. Owen; M. J. Hill; Eva Latymer; A. Graham Low; Arthur N. Mason


Biochemical Society Transactions | 1978

The Degradation of Taurocholic acid and Glycocholic acid by Pseudomonas spp. N.C.I.B. 10590

Michael E. Tenneson; Rodney F. Bilton; Arthur N. Mason


Biochemical Society Transactions | 1975

The coupling of anaerobic steroid dehydrogenation to nitrate reduction in Pseudomonas N.C.I.B. 10590 and Clostridium paraputrificum.

Peter J. Barnes; Rodney F. Bilton; Arthur N. Mason; Fresia Fernandez; M. J. Hill

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Rodney F. Bilton

Liverpool John Moores University

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