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Pretreatment incubation for culture and cryopreservation of Sabal embryos
Wen, B; Wang, RL
2010
Source PublicationPLANT CELL TISSUE AND ORGAN CULTURE
Volume102Issue:2Pages:237-243
AbstractZygotic embryos from mature seeds of Sabal jamaicensis, S. minor, S. umbraculifera and S. yapa were cultured in vitro and cryopreserved successfully. Seed pretreatment prior to embryo isolation was shown to be crucial. Soaking seeds in water or sowing on 1% agar followed by incubation at 30A degrees C for 1 day (S. jamaicensis, S. minor and S. umbraculifera) or 3 days (S. yapa only) prior to embryo isolation increased the percentage emergence of cultured embryos from less than 20% to more than 94%. Without this pretreatment, most isolated embryos turned brown and died soon after culture. Through preincubation combined with partial dehydration to 18-28% moisture content, direct freezing and rapid thawing, isolated embryos were successfully cryopreserved and 31-44% emergence was achieved from postthawed embryos for the four Sabal species.
KeywordCryopreservation Embryo Culture Preincubation Sabal Zygotic Embryo
Document Type期刊论文
Identifierhttps://ir.xtbg.ac.cn/handle/353005/3846
Collection支撑系统
Recommended Citation
GB/T 7714
Wen, B,Wang, RL. Pretreatment incubation for culture and cryopreservation of Sabal embryos[J]. PLANT CELL TISSUE AND ORGAN CULTURE,2010,102(2):237-243.
APA Wen, B,&Wang, RL.(2010).Pretreatment incubation for culture and cryopreservation of Sabal embryos.PLANT CELL TISSUE AND ORGAN CULTURE,102(2),237-243.
MLA Wen, B,et al."Pretreatment incubation for culture and cryopreservation of Sabal embryos".PLANT CELL TISSUE AND ORGAN CULTURE 102.2(2010):237-243.
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