首页> 外国专利> THE METHOD OF CULTURING LIQUID STARTER OF BASIDOMYCETIS AND LIQUID STARTER

THE METHOD OF CULTURING LIQUID STARTER OF BASIDOMYCETIS AND LIQUID STARTER

机译:培养基础芽孢杆菌的液体发酵剂和液体发酵剂的方法

摘要

The present invention relates to a liquid spawn cultivation method of basidiomycetes and a liquid spawn thereof, and more particularly to a method capable of producing a large amount of liquid spawn useful for the cultivation of various mushrooms of high quality and a liquid spawn obtained by the method.;The present invention is a liquid culture method of common basidiomycetes, the pre-culture step (a) 2 ~ 7% (w / v) carbon source, 0.1 ~ 1.0% (w / v) nitrogen source, KH 2 PO 4 0 ~ 0.15 Inoculate the plated basidiomycetes in the preculture consisting of% (w / v), MgSO 4 · 7H 2 O 0-0.15% (w / v), and the remaining distilled water, and (b) the inoculated preculture Incubated at 80 ~ 200 rpm, 22 ~ 30 ℃ shaking culture in 6 to 8 days; The above liquid culture process was carried out by (a) carbon source 2-7% (w / v), nitrogen source 0.1-1.0% (w / v), KH 2 PO 4 0-0.15% (w / v), MgSO 4 7H 2 O 0 ~ 0.15% (w / v), and prepare a liquid culture consisting of the remaining distilled water, (b) aseptic auto-inoculation of the pre-inoculation source to the liquid culture solution, (c) the inoculated The liquid culture consists of aeration of the culture medium at 22-28 ° C. with sterilized air on the order of 0.1-1.0vvm for 5-12 days.;The present invention is characterized in that it is composed of a series of steps which are inseparably connected to the preculture process and the liquid culture process under stringent conditions, respectively, after collecting the prokaryote of basidiomycetes.
机译:本发明涉及一种担子菌的液体产卵方法及其液体产卵方法,更具体地说,涉及一种能够产生大量的液体产卵方法,用于栽培各种高质量的蘑菇,以及通过该方法获得的液体产卵方法。本发明是普通担子菌的液体培养方法,预培养步骤(a)为碳源2〜7%(w / v),氮源0.1〜1.0%(w / v),KH 2 PO 4 0〜0.15接种预培养的平板状担子菌,其中含%(w / v),MgSO 4 4 ·7H 2 < / sub> O 0-0.15%(w / v),并保留蒸馏水,和(b)接种的预培养物以80〜200 rpm,22〜30℃振荡培养6〜8天;通过(a)碳源2-7%(w / v),氮源0.1-1.0%(w / v),KH 2 PO 4进行上述液体培养过程 0-0.15%(w / v),MgSO 4 4 7H 2 O 0〜0.15%(w / v),并准备由剩余的蒸馏水,(b)将预接种源无菌自动接种到液体培养液中,(c)接种后的液体培养物包括在22-28°C下用无菌空气对培养基进行曝气本发明的特征在于它由一系列步骤组成,这些步骤在严格的条件下分别收集到预培养过程和液体培养过程,在收集之后经过5-12天。担子菌的原核生物。

著录项

  • 公开/公告号KR100204982B1

    专利类型

  • 公开/公告日1999-06-15

    原文格式PDF

  • 申请/专利权人 DONG-EUN DEVELOPMENT PROMOTION CO. LTD.;

    申请/专利号KR19970006920

  • 发明设计人 성재모;

    申请日1997-03-03

  • 分类号A01G1/04;

  • 国家 KR

  • 入库时间 2022-08-22 02:15:45

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