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Colchicine-induced tetraploidy in garlic (Allium sativum L.) and its effect on allicin concentration
Colchicine is known to affect the concentrations of metabolites by changing the ploidy level of the genome. Allicin is the most important, pharmaceutically-active metabolite in garlic (Allium sativum L.) and is known for its anti-bacterial, anti-fungal, and anti-atherosclerotic activities. Duplicati...
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Published in: | The journal of horticultural science & biotechnology 2014-01, Vol.89 (5), p.585-591 |
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Main Authors: | , |
Format: | Article |
Language: | English |
Citations: | Items that cite this one |
Online Access: | Get full text |
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Summary: | Colchicine is known to affect the concentrations of metabolites by changing the ploidy level of the genome. Allicin is the most important, pharmaceutically-active metabolite in garlic (Allium sativum L.) and is known for its anti-bacterial, anti-fungal, and anti-atherosclerotic activities. Duplication of the diploid garlic genome was induced by treating garlic stem discs with 0.5% (w/v) colchicine. The tetraploids possessed thicker and darker-green leaves compared to untreated control plants and also showed pronounced differences in stomatal size. Leaves on the tetraploid clones exhibited smaller length-to-width ratios, but their leaf areas were up to three-times higher than in control diploid plants. These morphological characteristics were used as reliable phenotypic markers to screen for autotetraploid clones from a mixed population of polyploids and control diploid plants. In comparison to control diploid garlic plants, autotetraploid plants exhibited an average 30.7% increase in allicin concentration. The increase was measured indirectly as a significant increase in pyruvate concentration (87.15 ± 0.86 µmol g
-1
FW), which is a by-product of allicin biosynthesis. This study demonstrated that autotetraploids of garlic with increased concentrations of secondary metabolites can be generated successfully through in vitro stem-disc culture with 0.5% (w/v) colchicine. |
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ISSN: | 1462-0316 2380-4084 |
DOI: | 10.1080/14620316.2014.11513124 |