PLANT PHYSIOLOGY , Vol 110, Issue 4 1215-1222, Copyright © 1996 by American Society of Plant Biologists
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BIOCHEMISTRY AND ENZYMOLOGY |
Characterization of a Mutant of Chlamydomonas reinhardtii That Uses L-Methionine-S-Sulfoximine and Phosphinothricin as Nitrogen Sources for Growth
A. R. Franco, M. E. Diaz, M. Pineda and J. Cardenas
Departamento de Bioquimica y Biologia Molecular, Facultad de Ciencias, Universidad de Cordoba, E-14071 Cordoba, Spain
A strain of Chlamydomonas reinhardtii, named ARF-1, which grows with the
glutamine synthetase (GS) inhibitor L-methionine-S-sulfoximine (MSX), has
been isolated and characterized. Mutant ARF-1 is affected at a single and
dominant gene, tentatively assigned to the allele msr-1-2. Neither the
uptake of ammonia nor the two GS isoenzyme activities of the mutant were
affected by MSX in vivo. GS activities, however, were fully abolished in
vitro, thus suggesting that neither GS isoform was an altered enzyme
resistant to the inhibitor. Resistance to MSX does not seem to be due to
either a defect in a permease responsible for the transport of MSX or
over-expression of GS activity, nor did we find an alternative enzymatic
pathway for the assimilation of ammonium. Resistance was independent of the
nitrogen source used and was strongly enhanced by the addition of acetate.
Unlike the parental strain, mutant ARF-1 can degrade and utilize MSX as the
sole nitrogen source for growth, which could account for the observed
resistance. Thus, this mutant can be classified as a novel type of
MSX-resistant mutant. This mutant can also use phosphinothricin, methionine
sulfone, or methionine sulfoxide as the sole sources of nitrogen. This
capability cosegregated in the genetic crosses and was also observed in all
the diploids isolated. An MSX/[alpha]-ketoglutarate aminotransferase
activity, not present in the parental strain 305, was detected in mutant
ARF-1 cells. Therefore, we propose that the locus msr-1-2 either codes for
this transaminase activity or its product gene is necessary to express this
transaminase activity.