Please use this identifier to cite or link to this item: https://scholarbank.nus.edu.sg/handle/10635/111876
Title: Ethylene inhibitors enhanced de novo shoot regeneration from cotyledons of Brassica campestris ssp. chinensis (Chinese cabbage) in vitro
Authors: Chi, G.-L. 
Pua, E.-C. 
Keywords: Brassica campestris ssp. chinensis
Chinese cabbage
ethylene inhibitors
plant regeneration
tissue culture
Issue Date: 1989
Citation: Chi, G.-L.,Pua, E.-C. (1989). Ethylene inhibitors enhanced de novo shoot regeneration from cotyledons of Brassica campestris ssp. chinensis (Chinese cabbage) in vitro. Plant Science 64 (2) : 243-250. ScholarBank@NUS Repository.
Abstract: A tissue culture system for obtaining high frequency shoot regeneration of Brassica campestris ssp. chinensis cv. Speedy and 2B-21-64 was optimized via judicious selection of explants and manipulation of culture medium with respect to hormonal combination and addition of AgNO3, Ag2SO4, aminoethyoxyvinylglycine (AVG), aminooxyacetic acid (AOA) or 2,4-dinitrophenol (DNP). Three-day-old cotyledons of both cultivars grown on Murashige and Skoog's medium supplemented with 4.4-17.6 μM benzyladenine and 2.7-5.4 μM naphthaleneacetic acid (NAA) in the presence of 7.5-60 μM AgNO3 or Ag2SO4 or medium containing 8.8 μM BA, 5.4 μM NAA and 0.1-10 μM AVG formed shoots at 70-85% frequency after 3-4 weeks, whereas explants grown in the absence of Ag+ or AVG or in the presence of AOA or DNP were poorly regenerative (20-30%). Shoot tips originating from regenerants and seedlings rooted equally well in hormone-free medium or medium containing 0.05-5 μM indolebutyric acid. All rooted shoots were successfully acclimatized. The acclimatized plants were phenotypically indistinguishable from those derived from seeds. © 1989.
Source Title: Plant Science
URI: http://scholarbank.nus.edu.sg/handle/10635/111876
ISSN: 01689452
Appears in Collections:Staff Publications

Show full item record
Files in This Item:
There are no files associated with this item.

Google ScholarTM

Check


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.