首页> 外国专利> LIQUID COMPOSITION OF MICROORGANISMS FOR BIOREMEDIATION OF HYDROCARBON-CONTAMINATED SOIL, METHOD OF PREPARING THE SAME, AND BIOREMEDIATION USING THE SAME

LIQUID COMPOSITION OF MICROORGANISMS FOR BIOREMEDIATION OF HYDROCARBON-CONTAMINATED SOIL, METHOD OF PREPARING THE SAME, AND BIOREMEDIATION USING THE SAME

机译:烃污染土壤生物修复的微生物的液体组成,制备方法及使用该微生物修复的微生物

摘要

A liquid composition of microorganisms for remediation of oil-contaminated soil is provided to increase degradation activities of oil, a method of preparing the composition is provided, and a method for prompt bioremediation of oil-contaminated soil using the composition is provided. A liquid composition of microorganisms for remediation of oil-contaminated soil is characterized in that a culture fluid of a high growth strain which reaches a stationary phase within 10 hours having degradation ability of oil separated from oil-contaminated soil and a culture fluid of a low growth strain with a growth rate slower than that of the high growth strain are mixed with each other. A method of preparing a liquid composition of microorganisms for remediation of oil-contaminated soil comprises the steps of: sorting and selecting a strain with oil degrading ability from oil-contaminated soil; separating a strain reaching a stationary phase within 10 hours as a high growth strain, and separating a strain reaching the stationary phase after 10 hours as a low growth strain according to the growth rate of the strain; culturing the high growth strain and the low growth strain in respective culture media; and mixing a culture fluid of the high growth strain with a culture fluid of the low growth strain. Further, 0.001 to 1 g of enzyme expression accelerator is comprised based on 1L of media in the culture media.
机译:提供了用于修复油污染的土壤的微生物的液体组合物以增加油的降解活性,提供了一种制备该组合物的方法,并且提供了一种使用该组合物迅速对油污染的土壤进行生物修复的方法。用于修复被油污染的土壤的微生物的液体组合物的特征在于,高生长菌株的培养液在10小时内达到固定相,该培养液具有从被油污染的土壤中分离的油的降解能力和低污染的培养液。生长速度比高生长菌株慢的生长菌株彼此混合。一种制备用于修复油污土壤的微生物液体组合物的方法,其包括以下步骤:从油污土壤中分选具有油降解能力的菌株。根据生长速度,将在10小时内到达固定相的菌株分离为高生长菌株,将在10小时后到达固定相的菌株分离为低生长菌株。在相应的培养基中培养高生长菌株和低生长菌株;将高生长菌株的培养液与低生长菌株的培养液混合。此外,基于培养基中的1L培养基,构成0.001〜1g的酶表达促进剂。

著录项

  • 公开/公告号KR20080046301A

    专利类型

  • 公开/公告日2008-05-27

    原文格式PDF

  • 申请/专利权人 SK ENERGY CO. LTD.;

    申请/专利号KR20060115553

  • 发明设计人 PARK CHEOL HEE;WOO SEUNG HAN;KIM JU HOE;

    申请日2006-11-22

  • 分类号B09C1/10;

  • 国家 KR

  • 入库时间 2022-08-21 19:53:41

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