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Biosynthesis of δ-Aminolevulinic Acid in Chlamydomonas reinhardtii
Author(s) -
Yun-Hwa L. Mau,
Wei-yeh Wang
Publication year - 1988
Publication title -
plant physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.554
H-Index - 312
eISSN - 1532-2548
pISSN - 0032-0889
DOI - 10.1104/pp.86.3.793
Subject(s) - transamination , chlamydomonas reinhardtii , biosynthesis , chlamydomonas , chemistry , substrate (aquarium) , molecule , stereochemistry , biochemistry , enzyme , biology , organic chemistry , mutant , gene , ecology
The first committed intermediate of chlorophyll biosynthesis, delta-aminolevulinic acid (ALA), is synthesized from glutamate in the plant cell. The last step of ALA synthesis is a transamination reaction which converts glutamate-1-semialdehyde (GSA) to ALA. The mechanism of the transamination was examined by using glutamate, specifically labeled with either 1-(13)C or (15)N, as substrate for ALA synthesis. After incubating with crude enzymes extracted from Chlamydomonas reinhardtii, the distribution of labels in purified ALA molecules was examined by nuclear magnetic resonance spectroscopy and gas chromatography-mass spectrometry. We found that both isotopes were present in the same ALA molecule. We interpret the results to mean that intermolecular transamination occurs during the conversion of GSA to ALA.

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