首页> 外文期刊>Protoplasma: An International Journal of Cell Biology >Enhanced expression of ginsenoside biosynthetic genes and in vitro ginsenoside production in elicited Panax sikkimensis (Ban) cell suspensions
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Enhanced expression of ginsenoside biosynthetic genes and in vitro ginsenoside production in elicited Panax sikkimensis (Ban) cell suspensions

机译:增强人参皂苷生物合成基因的表达和体外人参皂苷在引发的panax sikkimensis(禁令)细胞悬浮液中的表达

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摘要

Dual metabolite, i.e., ginsenoside and anthocyanin, co-accumulating cell suspensions of Panax sikkimensis were subjected to elicitation with culture filtrates of Serratia marcescens (SD 21), Bacillus subtilis (FL11), Trichoderma atroviridae (TA), and T. harzianum (TH) at 1.25% and 2.5% v/v for 1- and 3-week duration. The fungal-derived elicitors (TA and TH) did not significantly affect biomass accumulation; however, bacterial elicitors (SD 21 and FL11), especially SD 21, led to comparable loss in biomass growth. In terms of ginsenoside content, differential responses were observed. A maximum of 3.2-fold increase (222.2 mg/L) in total ginsenoside content was observed with the use of 2.5% v/v TH culture filtrate for 1 week. Similar ginsenoside accumulation was observed with the use of 1-week treatment with 2.5% v/v SD 21 culture filtrate (189.3 mg/L) with a 10-fold increase in intracellular Rg2 biosynthesis (31 mg/L). Real-time PCR analysis of key ginsenoside biosynthesis genes, i.e., FPS, SQS, DDS, PPDS, and PPTS, revealed prominent upregulation of particularly PPTS expression (20-23-fold), accounting for the observed enhancement in protopanaxatriol ginsenosides. However, none of the elicitors led to successful enhancement in in vitro anthocyanin accumulation as compared to control values.
机译:双代谢物,即人参皂苷和花青素,共累积Panax sikkimensis的细胞悬浮液被引发,诱导Serratia Marcescens(SD 21),枯草芽孢杆菌(FL11),richoderma Atroviridae(Ta),以及Harzianum(Th )1-和3周持续时间为1.25%和2.5%v / v。真菌衍生的Elictive(TA和Th)没有显着影响生物质积累;然而,细菌Elictors(SD 21和FL11),尤其是SD 21,导致生物质生长的比较损失。就人参皂苷含量而言,观察到差分反应。使用2.5%V / V Th培养滤液1周,最大地观察到总青核苷酸含量的3.2倍的增加(222.2mg / L)。通过使用1周处理,使用2.5%v / v Sd 21培养滤液(189.3mg / L)的培养滤液(189.3mg / L)增加了类似的人参皂苷累积,其细胞内RG2生物合成率为10倍(31mg / L)。关键人参皂甙生物合成基因的实时PCR分析,即FPS,SQS,DDS,PPD和PPT,揭示了特别pPT表达(20-23倍)的突出上调,占原子酰吡罗醇冠皂苷的观察到增强。然而,与对照值相比,任何elicitor都不会导致体外花青素积累的成功增强。

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  • 作者单位

    Cent Inst Med &

    Aromat Plants PO CIMAP Plant Biotechnol Div Council Sci &

    Ind Res Lucknow 226015 Uttar Pradesh India;

    Cent Inst Med &

    Aromat Plants PO CIMAP Microbiol &

    Entomol Div Council Sci &

    Ind Res Lucknow 226015 Uttar Pradesh India;

    Cent Inst Med &

    Aromat Plants PO CIMAP Microbiol &

    Entomol Div Council Sci &

    Ind Res Lucknow 226015 Uttar Pradesh India;

    Cent Inst Med &

    Aromat Plants PO CIMAP Plant Biotechnol Div Council Sci &

    Ind Res Lucknow 226015 Uttar Pradesh India;

    Cent Inst Med &

    Aromat Plants PO CIMAP Microbiol &

    Entomol Div Council Sci &

    Ind Res Lucknow 226015 Uttar Pradesh India;

    Cent Inst Med &

    Aromat Plants PO CIMAP Analyt Chem Div Council Sci &

    Ind Res Lucknow 226015 Uttar Pradesh India;

    Cent Inst Med &

    Aromat Plants PO CIMAP Plant Biotechnol Div Council Sci &

    Ind Res Lucknow 226015 Uttar Pradesh India;

    Cent Inst Med &

    Aromat Plants PO CIMAP Plant Biotechnol Div Council Sci &

    Ind Res Lucknow 226015 Uttar Pradesh India;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 细胞形态学;
  • 关键词

    Panax sikkimensis; Cell suspension; Ginsenoside; Trichoderma; Elicitation;

    机译:Panax sikkimensis;细胞悬浮液;人参皂苷;richoderma;elicitation;

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