Assessment of genetic stability of the germplasm lines of medicinal plant Scutellaria baicalensis Georgi (Huang-qin) in long-term, in vitro maintained cultures

被引:0
作者
Ali R. Alan
Hongyan Zeng
Akym Assani
Wendy L. Shi
Hannah E. McRae
Susan J. Murch
Praveen K. Saxena
机构
[1] University of Guelph,Department of Plant Agriculture
[2] University of British Columbia Okanagan,Department of Chemistry, I.K. Barber School of Arts and Sciences
来源
Plant Cell Reports | 2007年 / 26卷
关键词
Antioxidant; Flavonoid; Flow cytometry; Nuclear DNA content; Ploidy;
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中图分类号
学科分类号
摘要
An approach of combining flow cytometry (FCM) analysis with morphological and chemical profiling was used to assess the genetic stability and bioactive compound diversity in a Scutellaria baicalensis Georgi (Huang-qin) germplasm collection that was clonally maintained in in vitro for a period of over 6 years. Based on the FCM analysis of nuclei samples from young shoots, the nuclear DNA content of S. baicalensis was calculated as 0.84 pg/2C. FCM analysis showed no significant variation in the nuclear DNA contents and ploidy levels in the long-term in vitro maintained germplasm lines. Germplasm lines, acclimatized to ex vitro conditions, exhibited distinctive plant growth and bioactive compound production capacities. The high level of genetic stability observed in in vitro maintained S. baicalensis lines opens up a variety of opportunities such as allowing long-term aseptic preservation and easy distribution of well-characterized germplasm lines of this medicinal plant species. This study represents a novel approach for continuous maintenance, monitoring, and production of medicinal plant tissues with specific chemistry.
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页码:1345 / 1355
页数:10
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共 126 条
  • [1] Bennett MD(1995)Nuclear DNA amounts in angiosperms. Ann Bot 76 113-176
  • [2] Leitch IL(2003)Comparisons with Ann Bot 91 547-557
  • [3] Bennett MD(1992) (∼100 Mb) and Drosophila (∼175 Mb) using flow cytometry show genome size in Arabidopsis to be ∼157 Mb and ∼25% larger than the Arabidopsis genome initiative estimate of ∼125 Mb. Ann Bot 69 231-236
  • [4] Leitch IJ(1998)Flow cytometric determination of nuclear replication stages in tomato seeds during priming and germination. Plant Sci 133 221-229
  • [5] Price HJ(2001)Cytogenetic variability of in vitro regenerated Plant Cell Tiss Org Cult 64 145-157
  • [6] Johnston JS(1994) L. plants and their seed progenies. Acta Biotechnol 14 267-274
  • [7] Bino RJ(1997)Oxidative stress and physiological, epigenetic and genetic variability in plant tissue culture: implications for micropropagators and genetic engineers. Acta Biotechnol 17 83-90
  • [8] Devries JN(2005)The variability of the hypericin content in the regenerants of Mutat Res 578 15-22
  • [9] Kraak HL(2005). Ann Bot 95 99-110
  • [10] Van Pijlen JG(2003)Correlation between hypericin content and the ploidy of somaclones of Cytometry 51 127-128