Morphological characteristics, chemical and genetic diversity of kenaf (Hibiscus cannabinus L.) genotypes
2017
Ryu, J., Korea Atomic Energy Research Institute, Jeongup, Republic of Korea | Kwon, S.J., Korea Atomic Energy Research Institute, Jeongup, Republic of Korea | Kim, D.G., Korea Atomic Energy Research Institute, Jeongup, Republic of Korea | Lee, M.K., Korea Atomic Energy Research Institute, Jeongup, Republic of Korea | Kim, J.M., Korea Atomic Energy Research Institute, Jeongup, Republic of Korea | Jo, Y.D., Korea Atomic Energy Research Institute, Jeongup, Republic of Korea | Kim, S.H., Korea Atomic Energy Research Institute, Jeongup, Republic of Korea | Jeong, S.W., Korea Atomic Energy Research Institute, Jeongup, Republic of Korea | Kang, K.Y., Korea Atomic Energy Research Institute, Jeongup, Republic of Korea | Kim, S.W., Korea Atomic Energy Research Institute, Jeongup, Republic of Korea | Kim, J.B., Korea Atomic Energy Research Institute, Jeongup, Republic of Korea | Kang, S.Y., Korea Atomic Energy Research Institute, Jeongup, Republic of Korea
The kenaf plant is used widely as food and in traditional folk medicine. This study evaluated the morphological characteristics, functional compounds, and genetic diversity of 32 kenaf cultivars from a worldwide collection. We found significant differences in the functional compounds of leaves from all cultivars, including differences in levels of chlorogenic acid isomer (CAI), chlorogenic acid (CA), kaempferol glucosyl rhamnoside isomer (KGRI), kaempferol rhamnosyl xyloside (KRX), kaemperitrin (KAPT) and total phenols (TPC). The highest TPC, KAPT, CA, and KRX contents were observed in the C22 cultivars. A significant correlation was observed between flowering time and DM yield, seed yield, and four phenolic compounds (KGRI, KRX, CAI, and TPC) (P less than 0.01). To assess genetic diversity, we used 80 simple sequence repeats (SSR) primer sets and identified 225 polymorphic loci in the kenaf cultivars. The polymorphism information content and genetic diversity values ranged from 0.11 to 0.79 and 12 to 0.83, with average values of 0.39 and 0.43, respectively. The cluster analysis of the SSR markers showed that the kenaf genotypes could be clearly divided into three clusters based on flowering time. Correlations analysis was conducted for the 80 SSR markers; morphological, chemical and growth traits were found for 15 marker traits (corolla, vein, petal, leaf, stem color, leaf shape, and KGRI content) with significant marker-trait correlations. These results could be used for the selection of kenaf cultivars with improved yield and functional compounds.
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