首页> 外国专利> A PROCESS OF PREPARATION OF TISSUE CULTURE MEDIUM FOR ENHANCING IN-VITRO PLANTLET REGENERATION IN AIR YAM PLANT USING BACTERIAL CULTURE SUPERNATANT.

A PROCESS OF PREPARATION OF TISSUE CULTURE MEDIUM FOR ENHANCING IN-VITRO PLANTLET REGENERATION IN AIR YAM PLANT USING BACTERIAL CULTURE SUPERNATANT.

机译:利用细菌培养上清液制备组织培养介质以增强山药体外植株再生的方法。

摘要

This invention relates to a process of preparation of tissue culture medium for enhancing in-vitro plantlet regeneration in air yam plant using bacterial culture supernatant, in place of chemical growth promoter, comprising the steps of; growing Azotobacter chroococcum strain (A chroccoccum) in Jensen medium and/or Gluconacetobacter diazotrophicus strain (G. diazotorphicus) grown in LGI medium given by Covalcante and Dobereiner; adding to both media 75-125 mg/1 D,L tryptophan preferably 100 mg/1 as precursor of indoleacetic Acid (IAA); characterized in that centrifuging the bacterial culture after 4-8 days preferably 4 days for G. diazotrophicus medium and 8 days for A. chroococcum medium at 10,000 rpm for 18-25 minutes preferably 20 minutes to obtain Culture Supernatant; adding Culture Supernatant, obtained from step (ii), to Murashige and Skoog basal medium for nodal explants' growth; wherein Culture Supernatant supplemented medium regenerates healthy roots and shoots simultaneously in 25-30 days as compared to normal 40-45 days.
机译:本发明涉及一种使用细菌培养上清液代替化学生长促进剂来制备增强空气山药植物离体苗再生的组织培养基的方法,该方法包括以下步骤:在Jensen培养基中生长的绿脓杆菌菌株(A crococcum)和/或在Covalcante和Dobereiner给予的LGI培养基中生长的重氮糖杆菌细菌重氮菌(G. diazotorphicus);向两种介质中加入75-125 mg / 1 D,L色氨酸,优选100 mg / 1作为吲哚乙酸(IAA)的前体;其特征在于,将重氮营养芽孢杆菌培养基在4-8天,优选4天,对球形芽孢杆菌培养基在10,000rpm下离心细菌培养物18-25分钟,优选20分钟,以获得培养上清液;将步骤(ii)中获得的培养上清液添加到Murashige和Skoog基础培养基中,以促进结节外植体的生长;其中添加了培养上清液的培养基与正常的40-45天相比,可在25-30天同时再生健康的根和芽。

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