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通过玻璃化法对日本地生兰花(白芨)合子胚进行冷冻保存。

Cryopreservation of zygotic embryos of a Japanese terrestrial orchid (Bletilla striata) by vitrification.

作者信息

Ishikawa K, Harata K, Mii M, Sakai A, Yoshimatsu K, Shimomura K

机构信息

Plant Cell Technology Laboratory, Faculty of Horticulture, Chiba University, 648 Matsudo, Matsudo-City, Chiba 271, Japan Fax no.: +81-473-66-2234 E-mail:

1-5-23, Asao-cho, Kita-ku, Sapporo-City, Hokkaido 001, Japan, , , , , , JP.

出版信息

Plant Cell Rep. 1997 Sep;16(11):754-757. doi: 10.1007/s002990050314.

Abstract

The seeds of a Japanese terrestrial orchid (Bletilla striata Rchb.f.) were germinated and cultured on solidified new Dogashima (ND) medium for 10 days. These embryos were then precultured on ND medium supplemented with 0.3 M sucrose for 3 days at 25°C in continuous dark. The embryos were then overlaid with a mixture of 2 M glycerol and 0.4 M sucrose for 15 min at 25°C and finally dehydrated with highly concentrated vitrification solution (PVS2) for 3 h at 0°C prior to immersion into liquid nitrogen for 30 min. After rapid warming, the embryos were washed with liquid ND medium supplemented with 1.2 M sucrose for 20 min and then plated on ND medium. Successfully vitrified and warmed embryos developed into normal plantlets. The rate of plant regeneration amounted to about 60%. This vitrification method appears to be a promising technique for cryopreservation of orchids.

摘要

将日本地生兰花(白及)的种子在固化的新小笠原(ND)培养基上萌发并培养10天。然后将这些胚在补充有0.3 M蔗糖的ND培养基上于25°C连续黑暗条件下预培养3天。接着将胚在25°C下用2 M甘油和0.4 M蔗糖的混合物覆盖15分钟,最后在浸入液氮30分钟之前,于0°C用高浓度玻璃化溶液(PVS2)脱水3小时。快速复温后,将胚用补充有1.2 M蔗糖的液体ND培养基洗涤20分钟,然后接种到ND培养基上。成功玻璃化和复温的胚发育成正常植株。植株再生率约为60%。这种玻璃化方法似乎是一种很有前景的兰花冷冻保存技术。

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