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利用霍山石斛原球茎长期培养生产活性多糖的稳定性

Production stability of active polysaccharides of Dendrobium huoshanense using long-term cultures of protocorm-like bodies.

作者信息

Zha Xue-Qiang, Luo Jian-Ping

机构信息

School of Biotechnology and Food Engineering, Hefei University of Technology, Hefei, People's Republic of China.

出版信息

Planta Med. 2008 Jan;74(1):90-3. doi: 10.1055/s-2007-993762. Epub 2007 Dec 19.

DOI:10.1055/s-2007-993762
PMID:18095217
Abstract

In this study, the production stability of active polysaccharides in protocorm-like bodies (PLBs) induced from the seedling segments of Dendrobium huoshanense C. Z. Tang et S. J. Cheng was investigated during long-term subculture. Subcultures were conducted once every 30 days. With an average inoculum of 39 g/L fresh PLBs, the increase in biomass ranged from 95.7 g/L to 103.9 g/L in fresh weight and 3.2 g/L to 3.4 g/L in dry weight during eighteen continuous subcultures while polysaccharide content in PLBs was from 0.8 mg/g Fw (mg polysaccharide per gram PLBs in fresh weight) to 1.0 mg/g Fw. In addition, polysaccharides from all cultures showed a similar potential of stimulating interferon gamma (IFN-gamma) release in the supernatant of splenocytes and tumor necrosis factor alpha (TNF-alpha) release in the supernatant of peritoneal macrophages. To elucidate the genetic basis of polysaccharide production stability in long-term subculture of PLBs, the genetic fingerprints by RAPD were further analyzed using plantlets from PLB development. Results showed that there is no evidence of genetic variation both within the plantlets from the different subcultures of PLBs and between long-term subcultures and the donor plants.

摘要

本研究对霍山石斛(Dendrobium huoshanense C. Z. Tang et S. J. Cheng)幼苗切段诱导形成的原球茎(PLBs)在长期继代培养过程中活性多糖的生产稳定性进行了研究。每30天进行一次继代培养。以平均接种量39 g/L新鲜PLBs计,在连续18次继代培养期间,鲜重生物量增加范围为95.7 g/L至103.9 g/L,干重增加范围为3.2 g/L至3.4 g/L,而PLBs中的多糖含量为0.8 mg/g Fw(每克鲜重PLBs中的多糖毫克数)至1.0 mg/g Fw。此外,所有培养物中的多糖在脾细胞上清液中刺激γ干扰素(IFN-γ)释放以及在腹腔巨噬细胞上清液中刺激肿瘤坏死因子α(TNF-α)释放方面均显示出相似的潜力。为阐明PLBs长期继代培养中多糖生产稳定性的遗传基础,利用PLB发育形成的植株对RAPD产生的遗传指纹进行了进一步分析。结果表明,无论是来自PLBs不同继代培养的植株内部,还是长期继代培养植株与供体植株之间,均无遗传变异的证据。

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