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马尾树愈伤组织的诱导与褐化控制研究 被引量:3

Experimental Study on the Induction and Browning Control of Rhoiptelea chiliantha Callus
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摘要 [目的]为保护和开发利用马尾树资源提供科学的理论依据。[方法]以MS为基本培养基,用IBA和6-BA以及不同浓度配比的抗褐化剂AC、VC和Na2S2O3诱导马尾树愈伤组织。[结果]在诱导过程中马尾树愈伤组织的褐化现象很突出,接种几小时后外植体周围即出现褐化物质。以冬芽和春芽为外植体时,这些抗褐化剂均不起作用。以嫩叶为外植体时,抗褐化剂AC起显著作用。3种抗褐化剂组合使用时,仅AC的作用显著,而VC和Na2S2O3的作用不显著。仅在以嫩叶为外植体的培养中诱导出了愈伤组织。MS+IBA 1.5mg/L+6-BA2.5 mg/L+AC3.0 g/L最适于马尾树嫩叶愈伤组织的诱导。[结论]马尾树的嫩叶可用于诱导愈伤组织,这为马尾树的细胞培养奠定了基础。 [Objective] The purpose was to supply scientifically theoretical basis for protecting and exploiting Rhoiptelea chiliantha Dieis et Hang-Mazz resources. [Method] With MS as basic media, IBA, 6-BA and anti-browning agents AC, Vc and Na2S2O3 with different conch, ratios were used to induce R. chiliantha callus. [Result] The browning phenomenon ofR. chiliantha callus was very outstanding in the induction course and the browning substance appeared around the explant after several hours since inoculation. With winter and spring buds as explants, these anti -browning agents bad no effect. With tender leaves as explants, the anti -browning agent AC bad significant effect. When the combination of these 3 anti -browning agents was used, only the effect of AC was significant and that of Vc and Na2S2O3 were not significant. Only in the culture with tender leaves as explants, the callus was induced. MS + IBA 1.5 mg/L + 6-BA 9.5 mg/L + AC 3.0 g/L was optimum for the callus induction of tender leaves in R. chiliantha. [Conclusion] The tender leaves of R. chiliantha could be used to induce the callus, which laid a foundation for the cell culture of R. chiliantha.
作者 郭治友
出处 《安徽农业科学》 CAS 北大核心 2008年第11期4429-4430,共2页 Journal of Anhui Agricultural Sciences
基金 黔南州科技局资助项目(2004NY04)
关键词 马尾树 褐化控制 愈伤组织诱导 Rhoiptelea chiliantha Dieis et Hang-Mazz Browning control Callus induction
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  • 1张虹.梨树组织培养研究的进展[J].广西热带农业,2004(5):12-16. 被引量:15
  • 2吴征镒.中国种子植物属的分布区类型[J].云南植物研究,1991,(7):1-139.
  • 3周政贤.雷公山自然保护区科学考察集[M].贵阳:贵州人民出版社,1989.11-205.
  • 4韩碧文 刘淑兰.核桃组织培养.木本植物组织培养及其应用[M].北京高等教育出版社,1986.456-465.
  • 5Hu CY, wans Pj Mcristem, shoot tip and bud cultures In: Emvans DA sharp wR Ammarato Pveud (eds) .Hand - book of plant cell cu]ture(voluml) New York: Mscmillan Publishing co A Division of Macmillan Ins. 1983, 177-228.
  • 6Faust M, Physiology of Femperate Zone Fuit Trees New York: wiley-Interscience 1989, 110-114.
  • 7Debrgh Pc Read PE Micropagation In: Debergh Pc, Zimmerman RH (eds), Micropropagation Kiuwer Academic Publishers 1991, 1- 13.
  • 8Lshii M, Uemoto S, Fujieda K studies on tissue culture in cauceya species Ⅱ Preventive methods for the browming of er- planted tissue.J Jap soc Hort Sci, 1979, 48:199-204.
  • 9Pierik RLM Inlitro culture of Higher Plant Mattings Ni - jhoff Publishers,1987.
  • 10Creasey LL The increase in phenylalanine ammonialyase ac - tivity in strawberry leaf disks and its eor~ation with flavonoid synthesis phytocben 1968, 7:441-446.

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