Abstract

Mutant strains of the cyanobacterium Synechococcus sp. PCC 7942 that are resistant to the herbicides norflurazon and fluridone were analyzed. These herbicides inhibit phytoene desaturase, a key enzyme in the carotenoid biosynthetic pathway. In three mutants the phenotype was related to specific point mutations in pds, the gene encoding phytoene desaturase. Since the resistance was manifested in a cell-free carotenogenic assay, it is evident that the predicted amino acid changes in the target protein alter the enzyme-herbicide interactions. In addition, the mutations also reduced the in vitro activity of phytoene desaturase. Increased levels of the substrate phytoene, accompanied by a reduction in colored carotenoids, were detected in cells of each of the mutant strains. A correlation was established between the degree of increase in the steady-state levels of phytoene and the extent of reduction in total carotenoid content in the cells. These two phenomena in turn are correlated with the rate of enzymatic activity of phytoene desaturase that was measured in vitro. Hence we deduce that phytoene desaturation is a rate-limiting step in carotenogenesis in cyanobacteria. Support for this conclusion is obtained from analysis of cells of an additional mutant strain, which overexpress phytoene desaturase due to a deletion mutation in the promoter region of pds. Cells of this mutant contained more colored carotenoids than the wild-type and were resistant to herbicides that inhibit phytoene desaturase.

Highlights

  • Increased levels of thesubstrate phytoene, accomenzyme that utilizes both identical halves of the symmetrical phytoene as a substrate to produce {-carotene, with phytofluene as an intermediate (Linden et al, 1991; Pecker et al, 1992)

  • Support for this conclusion is ob- Subsequent analysis of pds from both tomato and Dunaliella tained from analysis of cells of an additional mutant bardawil has shown that thededuced amino acid sequence of strain, which overexpress phytoene desaturase due to PDS is highly conserved in cyanobacteria, alga, and plants a deletion mutation in the promotrergion of pds

  • The isogenic strains of the above herbicide-resistant mutants were was extracted from a single colony of cells from each of the strains by the procedure described by Ohad and Hirschberg (1992).The pds gene was amplified by the polymerase chain reaction (PCR) using

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Summary

MATERIALS AND METHODS

Ylgeranyl pyrophosphate to yield the colorless 15-cis-phy- Strains-The wild-type and herbicide-resistant strains of the unitoene. This article must be hereby marked "advertisement" in accordance with 18 U.S.C. The abbreviations used are: PDS, phytoene desaturase; DMF, N,N-dimethylformamide; PBS, phosphate-buffered saline; pds, gene encoding phytoene desaturase; HPLC,high performance liquid chromatography; PCR, polymerase chain reaction. The abbreviations used are: PDS, phytoene desaturase; DMF, N,N-dimethylformamide; PBS, phosphate-buffered saline; pds, gene encoding phytoene desaturase; HPLC,high performance liquid chromatography; PCR, polymerase chain reaction The isogenic strains of the above herbicide-resistant mutants were was extracted from a single colony of cells from each of the strains by the procedure described by Ohad and Hirschberg (1992).The pds gene was amplified by the polymerase chain reaction (PCR) using. HPLC apparatus, consisting of a L6200 pump, L3000 multichannel photodetector, and D6000 interphase was used, employingan isocratic

RESULTS
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