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Curcuma L. is an economically important genus in the family Zingiberaceae. Many species are grown as medicinal, culinary, and ornamental crops. As a result of their high morphological diversity and small chromosome sizes, chromosome numbers and species relationships of Chinese Curcumas remain debated. This study examined chromosome numbers of 15 populations representing 11 species of Curcuma from China. Results showed that only Curcuma flaviflora S. Q. Tong was diploid with 2n = 2x = 42 and C. kwangsiensis S. G. Lee & C. F. Liang was tetraploid with 2n = 4x = 84. The other species were triploid (2n = 3x = 63). The study indicated that the basic chromosome number of Curcuma from China could be x = 21. The diploid C. flaviflora produced viable seeds, which was the main means for propagation. The tetraploid and the triploids produced no seeds and relied on rhizomes for propagation. Chromosome sizes of all species were small, ranging from 0.5 to 2.1 μm, which prevented karyotype analysis. The fact that nine of 11 species studied were triploid indicates that triploidy may have some type of competitive advantage over the diploid and tetraploid. In addition, the triploids are popular commercially because of abundant rhizome production and this may contribute to their wide distributions.
Leaf color mutants play an important role in our understanding of chlorophyll biosynthesis and catabolism. In this study, we obtained a yellow-green leaf mutant hy in an ethyl methanesulfonate mutagenized population of chinese cabbage (Brassica rapa ssp. pekinensis). The hy phenotype was controlled by a recessive allele at a single locus. The intrinsic photochemical activity of photosystem II (PSII) is impaired in hy, suggesting that absorbed light energy is not efficiently transferred from the light-harvesting complexes antenna to the PSII reaction centers and dissipated as heat or fluorescence. We measured chlorophyll content and chlorophyll precursors and analyzed the expression of key genes in the chlorophyll synthetic pathway in hy and wild type. The mutation phenotype was consistent with inhibited expression of chlorophyll a oxygenase (CAO) gene in the chlorophyll synthetic pathway. In mutant hy, CAO cDNA was cloned so that a C to T mutation at 1099 bp caused a conserved proline (Pro) to serine (Ser) mutation at the 367th amino acid in C-domain, which changed the secondary structure of CAO protein. We speculate that the mutation amino acid changed in the C-domain may affect the catalytic function in mutant CAO.