Effect of Colchicine on the Induction of Prunella vulgaris for. albiflora Nakai

This study was conducted to find out the effective induction method of tetraploid plants to obtain potential data for cultivating superior varieties by colchicine treatment. The seed germination were decreased by the higher concentration of colchicine treatment and longer soaking time. A total of 90...

Full description

Saved in:
Bibliographic Details
Published inKorean journal of crop science Vol. 60; no. 1; pp. 107 - 113
Main Authors Kwon, S.J., Woosong College, Daejeon, Republic of Korea, Roy, S.K., Chungbuk National University, Cheongju, Republic of Korea, Cho, K.Y., Woosong College, Daejeon, Republic of Korea, Moon, Y.J., Woosong College, Daejeon, Republic of Korea, Woo, S.H., Chungbuk National University, Cheongju, Republic of Korea, Kim, H.H., Woosong College, Daejeon, Republic of Korea
Format Journal Article
LanguageEnglish
Published 한국작물학회 31.03.2015
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:This study was conducted to find out the effective induction method of tetraploid plants to obtain potential data for cultivating superior varieties by colchicine treatment. The seed germination were decreased by the higher concentration of colchicine treatment and longer soaking time. A total of 907 individuals were germinated in 16 treated plots except control (untreated plot) and 28 tetraploids were induced which was about 3.1% of the number of seed germinated. The plant regeneration rate by colchicine treatment on explant of Prunella vulgaris for. albiflora Nakai under in vitro culture was decreased with the higher concentration of colchicine. While a total of 312 individuals were regenerated in all treatments, the explant was soaked in more than 0.05% for over 1 hour, tetraploid could be obtained. In particular, for the soaking treatment in 0.05% for 6 hours and 12 hours, 37 tetraploids were induced, which was about 57.8% of the number of plant regenerated. In accordance with the observation on doubling of DNA contents in leaf in order to identify polyploid, the peak DNA content of G1 phase was 101.3 for diploid and 197.2 for tetraploid. The result confirmed the doubling of DNA content. Furthermore, the number of chloroplasts per guard cell depending on polyploid was around 10 in diploid and 19.3 in tetraploid, which was around 1.9 times as much as diploid.
Bibliography:F01
http://www.cropbio.or.kr/
G704-000328.2015.60.1.017
ISSN:0252-9777
2287-8432
DOI:10.7740/kjcs.2014.60.1.107