Masters Theses

Abstract

"A survey of the ability of basidiomycetes to convert tryptophan, tryptamine and indole acetic acid to other acidic indoles has been made.

The product formed from tryptamine by Tricholoma nudum was identified as indole acetic acid. The product formed by Cantharellus cibarius from D-tryptophan was identified as N-acetyl-D-tryptophan. The products were purified and identified by means of paper chromatography, thin layer chromatography, infrared spectroscopy and melting points.

The conversion of tryptamine and D-tryptophan was also studied in cultures of Leucopaxillus paradoxus, Hygrophorus conicus and Naucoria confragosa. H. conicus, L. paradoxus and N. confragosa transformed tryptamine and indole acetic acid into oxindole acetic acid. L. paradoxus and N. confragosa also transformed D-tryptophan to oxindole acetic acid, but in poor yield. Two unidentified indole compounds were found in the culture media of L. paradoxus and N. confragosa grown on tryptamine.

Another product formed from tryptamine and indole acetic acid by T. nudum and N. confragosa was identified as 5-hydroxyindole acetic acid. T. nudum also transformed N,N-dimethyl-tryptamine into indole acetic acid and 5-hydroxy-indole acetic acid, but no transformation was observed with either α -ethyl- or α -methyl-tryptamine

An attempt to develop an assay method for the mono-amine oxidase of T. nudum was not notably successful"--Abstract, page i.

Advisor(s)

Siehr, Donald J.

Committee Member(s)

Conrad, Frank H., 1902-1983
Wixson, Bobby G.
Hanna, Samir B.

Department(s)

Chemistry

Degree Name

M.S. in Chemistry

Publisher

University of Missouri at Rolla

Publication Date

1967

Pagination

iv, 60 pages

Note about bibliography

Includes bibliographical references (pages 52-57).

Rights

© 1967 Chung-Ke Chang, All rights reserved.

Document Type

Thesis - Open Access

File Type

text

Language

English

Subject Headings

IndoleBasidiomycetesIndoleacetic acidHygrophorus

Thesis Number

T 1988

Print OCLC #

5981406

Electronic OCLC #

907300311

Included in

Chemistry Commons

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