CRYOPRESERVATION OF ENDANGERED WILD SPECIES, Aster altaicus var. uchiyamae Kitam, USING DROPLET-VITRIFICATION PROCEDURE

被引:0
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作者
Choi, Chung-Ho [1 ]
Popova, Elena [2 ]
Lee, Hyoeun [3 ]
Park, Sang-Un [4 ]
Ku, Jajung [5 ]
Kang, Jung-Hwa [6 ]
Kim, Haeng-Hoon [3 ]
机构
[1] Gyeonggi Do Forestry Environm Res Ctr, Osan Si 52319, South Korea
[2] Russian Acad Sci, Inst Plant Physiol, Natl Cell Culture Collect, Moscow, Russia
[3] Sunchon Natl Univ, Dept Well Being Resources, Sunchon 57922, South Korea
[4] Chungnam Natl Univ, Div Plant Sci & Resources, Daejeon 34134, South Korea
[5] Korea Forest Serv, Forest Policy Div, 189 Cheongsa Ro, Daejeon 35208, South Korea
[6] Hantaek Bot Garden Fdn, 2 Hantaek Ro, Yongin 17183, South Korea
关键词
ammonium nitrate; Asteraceae family; post-culture media; shoot tips; vitrification solution; IN-VITRO PROPAGATION; SHOOT TIPS; PLANT; RARE; MICROPROPAGATION; STORAGE; CELLS;
D O I
暂无
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
BACKGROUND: Aster altaicus var. uchiyamae Kitam is an endemic and endangered species in urgent need of a comprehensive conservation strategy. OBJECTIVE: To develop an efficient cryopreservation protocol using in vitro shoot tips to complement traditional conservation approaches in case seeds are not available or insufficient for conservation programs. METHODS: Shoot tips of in vitro plants were cryopreserved using a droplet-vitrification method following improvement of pre-culture, osmoprotection, vitrification solution (VS), unloading and post-culture treatments. The starting protocol included step-wise pre-culture with 10% and 17.5% sucrose for 55 h and 17 h, respectively, followed by osmoprotection with C4-35% (17.5% glycerol + 17.5% sucrose) for 30 min, and cryoprotection with B5-80% (40% glycerol + 40% sucrose) for 60 min. RESULTS: Shoot tips of A. altaicus were found to be moderately sensitive to the osmotic stress. Pre-culture and osmoprotection were not critical for the regeneration of cryopreserved explants when either of these treatments was applied. Osmoprotection with C4-35% on ice for 60 min followed by cryoprotection with A3-80%, a modified and diluted PVS2, on ice for 60 min resulted in the highest (65.3%) regeneration of cryopreserved shoot tips. Among alternative VSs tested, A3-80% and B5-80% were superior to PVS2 and PVS3 used under the same conditions. Step-wise recovery of shoot tips on ammonium-free medium followed by GA(3)-containing medium and medium without growth regulators were critical for the normal regeneration of both VS-treated and cryopreserved shoot tips. CONCLUSIONS: Cryopreservation of in vitro shoot tips using droplet-vitrification was developed as a complementary conservation approach for A. altaicus. Adjustment of the composition of regrowth media depending on recovery stage was important for the regeneration of healthy plants from cryopreserved shoot tips.
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页码:113 / 122
页数:10
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