http://chineseinput.net/에서 pinyin(병음)방식으로 중국어를 변환할 수 있습니다.
변환된 중국어를 복사하여 사용하시면 됩니다.
Md. Mahabubur Rahman,Muhammad Nurul Amin,Futoshi Ishiguri,Shinso Yokota,Rubaiyat Sharmin Sultana,Yuya Takashima,Kazuya Iizuka,Nobuo Yoshizawa 한국식물생명공학회 2009 Plant biotechnology reports Vol.3 No.3
A plantlet regeneration protocol was developed on pot-grown mature plants of Elaeocarpus robustus Roxb. cv. Dwarf from nodal and leaf explants. The best yield of adventitious shoots was achieved from the leaf-derived calli in a modified MS (MMS1, half strength of major salts, full strength of minor salts, and vitamins) medium containing 4.0 lM BA ? 4.0 lM Kn ? 0.5 lM NAA ? 15% coconut water (CW). The shoot multiplication rate was amplified about twofold per culture after the addition of 15% CW to the medium. The rate of shoot multiplication reached maximum at the 5th subculture, and it maintained this rate throughout the 3 subsequent subcultures. The best rooting in vitro was investigated by subculturing the microcuttings in an MMS2 (half strength of both major salts and minor salts and full strength of vitamins) medium containing 1.0 lM IBA in the dark for one initial week at 30C, followed by subculturing them in a plant-growth regulator (PGR)-free medium in the light. The plantlets raised in vitro were successfully established under ex vitro conditions. A plantlet regeneration protocol was developed on pot-grown mature plants of Elaeocarpus robustus Roxb. cv. Dwarf from nodal and leaf explants. The best yield of adventitious shoots was achieved from the leaf-derived calli in a modified MS (MMS1, half strength of major salts, full strength of minor salts, and vitamins) medium containing 4.0 lM BA ? 4.0 lM Kn ? 0.5 lM NAA ? 15% coconut water (CW). The shoot multiplication rate was amplified about twofold per culture after the addition of 15% CW to the medium. The rate of shoot multiplication reached maximum at the 5th subculture, and it maintained this rate throughout the 3 subsequent subcultures. The best rooting in vitro was investigated by subculturing the microcuttings in an MMS2 (half strength of both major salts and minor salts and full strength of vitamins) medium containing 1.0 lM IBA in the dark for one initial week at 30C, followed by subculturing them in a plant-growth regulator (PGR)-free medium in the light. The plantlets raised in vitro were successfully established under ex vitro conditions.