FEMS Microbiology Reviews · 1994 · 55 citations · 17 references
Life SciencesBiochemistryMolecular BiologyEnzymologyHeavy Metal ToxicologyMetabolismHeavy Metal BioaccumulationHeavy Metal MetabolismMetal ToxicityMolecular Basis Of ResistanceCadmium Toxicity MechanismsGlutathione BiosynthesisHeavy Metal Resistance GenesHeavy Metal Toxicity ToleranceHeavy Metal UptakeMetal-binding ProteinsPhytochelatin-mediated Tolerance
Plants and the fission yeast Schizosaccharomyces pombe synthesize small cadmium-binding peptides, called phytochelatins, in response to cadmium. Derived from glutathione (GSH: gamma-Glu-Cys-Gly), they have the general structure (gamma-Glu-Cys)nGly, where n is 2-11. In order to study the biosynthesis of phytochelatins, we used the mutagen N-methyl-N'-nitro-N nitrosoguanidine (MNNG) to select mutants with a lowered GSH content. GSH-deficient mutants show a Cd-sensitive phenotype, whereas resistance to Cu is only slightly influenced. These Cd-sensitive mutants contain 2-15% of the wild-type GSH level. For three mutants a lowered activity of gamma-glutamylcysteine synthetase was measured. One of the mutants was transformed to Cd-resistance and the complementing fragment was analyzed further. The complementing fragment hybridized with chromosome III. In the transformants, GSH content was restored up to wild-type levels, whereas the activity of gamma-glutamylcysteine synthetase was significantly increased compared with the wild-type. Possible mechanisms for Cd-resistance in the transformants are discussed.
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William H. Habig, M. Pabst, William B. Jakoby · Journal of Biological Chemistry · 1974 · 18.1K citations · Full text
Current protocols in molecular biology
R.K. Dudley · FEBS Letters · 1988 · 6K citations · Full text