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Method for culturing liquid spawn of basidiomycetes, its cultivation apparatus and liquid spawn

机译:担子菌液体产卵的培养方法,培养装置及液体产卵

摘要

The present invention relates to a liquid spawn cultivation method of basidiomycetes, a cultivation apparatus thereof, and a liquid spawn according to the method, and in particular, a cultivation method and a cultivation apparatus capable of producing a large amount of liquid spawn useful for the cultivation of various mushrooms of high quality and a cultivation apparatus and the method It relates to a liquid spawn obtained by.;The present invention is a liquid culture method of ordinary basidiomycetes, the pre-culture step (a) 2 to 7% (w / v) carbon source, 0.1 to 1.0% (w / v) nitrogen source, KH 2 PO 4 0 to 0.15 Inoculate the plated basidiomycete in the preculture consisting of% (w / v), MgSO 4 7H 2 0 0-0.15% (w / v), and the remaining distilled water, and (b) the inoculated preculture Incubated for 6 to 8 days in a shaker at 80 to 200 rpm and 22 to 30 ° C .; The above liquid culture process was carried out by (a) 2 to 7% (w / v) carbon source, 0.1 to 1.0% (w / v) nitrogen source, 0 to 0.15% (w / v) KH 2 PO 4 , MgSO 4 7H 2 0-0.15% (w / v), and a liquid culture medium consisting of the remaining distilled water, (b) aseptically inoculate the pre-inoculation source with the liquid culture solution, and (c) the inoculated above The liquid culture consists of aeration for 5 to 12 days at 5 to 100 rpm, the sterilized air at 0.1 to 1.0 vmv at 22 to 28 ° C.;The present invention is characterized in that after collecting the prokaryote of basidiomycetes, the pre-cultivation process and the liquid culture process consists of a series of inseparably connected series under strict conditions, respectively, and forcibly stirring the liquid culture. will be.
机译:本发明涉及担子菌的液体产卵栽培方法,其栽培设备以及根据该方法的液体产卵,特别是涉及一种能够产生大量可用于水产养殖的液体产卵的栽培方法和栽培设备。种高品质蘑菇的栽培及栽培装置和方法本发明涉及一种通过这种方法得到的液体产卵。本发明是普通担子菌的液体培养方法,预培养步骤(a)为2〜7%(w / v)碳源,0.1至1.0%(w / v)氮源,KH 2 PO 4 0至 0.15在接种前接种接种的担子菌,接种时应将%( w / v),MgSO 4 4 7H 2 0 0-0.15%(w / v)和剩余的蒸馏水,以及(b)接种的预培养物孵育6在80至200rpm和22至30℃的振动器中放置8天;通过(a)2至7%(w / v)的碳源,0.1至1.0%(w / v)的氮源, 0至 0.15%(w / v)进行上述液体培养过程v)KH 2 PO 4 ,MgSO 4 7H 2 0-0.15%(w / v)和由剩余蒸馏水组成的液体培养基,(b)用液体培养液无菌接种预接种源,和(c)以上接种。液体培养液由5到100 rpm的曝气时间5到12天组成本发明的特征在于,在收集担子菌的原核生物后,预培养过程和液体培养过程由一系列密不可分的系列组成,在严格条件下,强行搅拌液体培养液。将会。

著录项

  • 公开/公告号KR970027295A

    专利类型

  • 公开/公告日1997-06-24

    原文格式PDF

  • 申请/专利权人 양재훈;

    申请/专利号KR19970006922

  • 发明设计人 성재모;

    申请日1997-03-03

  • 分类号C12N1/14;

  • 国家 KR

  • 入库时间 2022-08-22 03:17:32

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