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1.
BMC Plant Biol ; 10: 133, 2010 Jun 28.
Article in English | MEDLINE | ID: mdl-20584316

ABSTRACT

BACKGROUND: Oxygenic photosynthesis is accompanied by the formation of reactive oxygen species (ROS), which damage proteins, lipids, DNA and finally limit plant yield. The enzymes of the chloroplast antioxidant system are exclusively nuclear encoded. During evolution, plastid and mitochondrial genes were post-endosymbiotically transferred to the nucleus, adapted for eukaryotic gene expression and post-translational protein targeting and supplemented with genes of eukaryotic origin. RESULTS: Here, the genomes of the green alga Chlamydomonas reinhardtii, the moss Physcomitrella patens, the lycophyte Selaginella moellendorffii and the seed plant Arabidopsis thaliana were screened for ORFs encoding chloroplast peroxidases. The identified genes were compared for their amino acid sequence similarities and gene structures. Stromal and thylakoid-bound ascorbate peroxidases (APx) share common splice sites demonstrating that they evolved from a common ancestral gene. In contrast to most cormophytes, our results predict that chloroplast APx activity is restricted to the stroma in Chlamydomonas and to thylakoids in Physcomitrella. The moss gene is of retrotransposonal origin.The exon-intron-structures of 2CP genes differ between chlorophytes and streptophytes indicating an independent evolution. According to amino acid sequence characteristics only the A-isoform of Chlamydomonas 2CP may be functionally equivalent to streptophyte 2CP, while the weakly expressed B- and C-isoforms show chlorophyte specific surfaces and amino acid sequence characteristics. The amino acid sequences of chloroplast PrxII are widely conserved between the investigated species. In the analyzed streptophytes, the genes are unspliced, but accumulated four introns in Chlamydomonas. A conserved splice site indicates also a common origin of chlorobiont PrxQ.The similarity of splice sites also demonstrates that streptophyte glutathione peroxidases (GPx) are of common origin. Besides a less related cysteine-type GPx, Chlamydomonas encodes two selenocysteine-type GPx. The latter were lost prior or during streptophyte evolution. CONCLUSION: Throughout plant evolution, there was a strong selective pressure on maintaining the activity of all three investigated types of peroxidases in chloroplasts. APx evolved from a gene, which dates back to times before differentiation of chlorobionts into chlorophytes and streptophytes, while Prx and presumably also GPx gene patterns may have evolved independently in the streptophyte and chlorophyte branches.


Subject(s)
Arabidopsis , Bryopsida , Chlamydomonas reinhardtii , Chloroplasts/enzymology , Peroxidases/genetics , Peroxidases/metabolism , Selaginellaceae , Amino Acid Sequence , Arabidopsis/enzymology , Arabidopsis/genetics , Arabidopsis/metabolism , Ascorbate Peroxidases , Bryopsida/enzymology , Bryopsida/genetics , Chlamydomonas reinhardtii/enzymology , Chlamydomonas reinhardtii/genetics , Data Mining , Databases, Protein , Exons/genetics , Gene Dosage , Gene Expression Regulation, Plant , Glutathione Peroxidase/chemistry , Glutathione Peroxidase/genetics , Glutathione Peroxidase/metabolism , Introns/genetics , Models, Molecular , Molecular Sequence Data , Peroxidases/chemistry , Peroxiredoxins/chemistry , Peroxiredoxins/genetics , Peroxiredoxins/metabolism , Phylogeny , Protein Structure, Tertiary , Seeds/genetics , Seeds/metabolism , Selaginellaceae/enzymology , Selaginellaceae/genetics , Sequence Alignment
2.
J Agric Food Chem ; 55(17): 7002-9, 2007 Aug 22.
Article in English | MEDLINE | ID: mdl-17655245

ABSTRACT

Resveratrol, a well-known phytoalexin and antioxidant, is produced by the action of stilbene synthase (STS) in some plant species. Hop (Humulus lupulus L.) plants of the Tettnang variety were transformed with a gene encoding for STS from grapevine. Under the control of the constitutive 35S cauliflower mosaic virus promoter, expression of the transgene resulted in accumulation of resveratrol and high levels of its glycosylated derivatives in leaves and inflorescences. Piceid, the predominant derivative, reached a concentration of up to 560 microg/g of fresh weight (f.w.) in hop cones, whereas no stilbenes were detected in nontransformed controls (wild-type). In transgenic plants the amounts of alpha- and beta-acids, naringenin chalcone, and prenylated flavonoids did not change significantly when compared with nontransformed plants. Transgenic plants showed normal morphology and flower development as did the nontransformed controls. The results clearly show that in hop constitutive expression of sts interferes neither with plant development nor with the biosynthesis of secondary metabolites relevant for the brewing industry. Since resveratrol is a well-known phytoalexin and antioxidant, sts transgenic hop plants could display enhanced pathogen resistance against microbial pathogens, exhibit new beneficial properties for health, and open new venues for metabolic engineering.


Subject(s)
Acyltransferases/genetics , Gene Expression , Humulus/genetics , Plants, Genetically Modified/enzymology , Stilbenes/metabolism , Vitis/enzymology , Humulus/enzymology , Resveratrol , Stilbenes/analysis , Vitis/genetics
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