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PMID: 14348193 Published · ppublish English Journal Article

BIOSYNTHESIS OF L-TYROSINE O-SULPHATE FROM THE METHYL AND ETHYL ESTERS OF L-TYROSINE.

The Biochemical journal ·Vol. 94 ·1965-02-00 ·Pages 331-6

JONES JG, DODGSON KS

Abstract

1. Rat-liver supernatant preparations are capable of achieving the biological sulphation of l-tyrosine methyl ester, the reaction proceeding maximally at a substrate concentration of 30 mm and at pH 7.0. 2. Two sulphated products are formed, one of which has been identified as l-tyrosine O-sulphate. On the basis of indirect evidence the other product can be assumed to be l-tyrosine O-sulphate methyl ester. 3. An enzyme present in rat-liver supernatant preparations is capable of converting l-tyrosine O-sulphate methyl ester into l-tyrosine O-sulphate. This enzyme is inhibited by l-tyrosine methyl ester. 4. l-Tyrosine ethyl ester also yields two sulphated products when used as an acceptor in the liver sulphating system. One of these has been identified chromatographically as l-tyrosine O-sulphate and the other may be presumed to be l-tyrosine O-sulphate ethyl ester.

Keywords
CHROMATOGRAPHY EXPERIMENTAL LAB STUDY HYDROGEN-ION CONCENTRATION ION EXCHANGE RESINS LIVER FUNCTION METABOLISM RATS SULFATES TYROSINE
MeSH Terms
Chromatography Esters Hydrogen-Ion Concentration Ion Exchange Resins Liver/physiology Metabolism Rats Research Sulfates Tyrosine
Chemicals
Esters Ion Exchange Resins Sulfates tyrosine methyl ester tyrosine O-sulfate Tyrosine ethyl tyrosine ester
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
JONES J G
DODGSON K S
References (12)
12 references, click to expand
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Article Info
Journal
The Biochemical journal
Abbr.
Biochem J
ISSN
0264-6021
Published
1965-02-00
Pages
331-6
Language
English
Region
England
NLM ID
2984726R
PMCID
PMC1206514
Subset
OM
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