生物学杂志 ›› 2022, Vol. 39 ›› Issue (3): 83-.doi: 10.3969/j.issn. 2095-1736.2022.03.083

• 研究报告 • 上一篇    下一篇

土霉素菌渣降解菌的筛选及应用条件优化

  

  1. 大连工业大学 生物工程学院, 大连 116034
  • 出版日期:2022-06-18 发布日期:2022-06-17
  • 通讯作者: 王红英,副教授,硕士生导师,研究方向为生物转化及开发利用,E-mail: 2002wanghongying@163.com
  • 作者简介:康润泽,硕士研究生,研究方向为微生物资源与利用,E-mail: 1924424853@qq.com
  • 基金资助:
    内蒙古自治区科技重大专项项目(222089)

Screening and optimization of application conditions of terramycin bacteria residue degrading bacteria

  1. School of Biological Engineering, Dalian Polytechnic University Dalian, Dalian 116034, China
  • Online:2022-06-18 Published:2022-06-17

摘要: 从土霉素生产菌渣中筛选出两株耐土霉素的霉菌M-1、M-2,对两株菌的酸、碱及土霉素的耐受性进行了研究,并以土霉素生产菌渣作为主要培养基成分,对其培养条件进行优化,同时考察两种菌株的产蛋白酶能力以及对土霉素生产菌渣活性成分的转化能力。结果表明:两种菌株在pH 3~7的培养基中均生长良好,其中霉菌M-1的耐酸性优于菌株M-2;1800 u/mL以下的土霉素浓度对两种菌株的生长没有产生明显的抑制作用;以5%菌渣悬浮液为培养基对菌株进行培养时,两种菌株均表现出较好的产蛋白酶特性,菌株M-1在最优培养条件下其产蛋白酶活力达到99.33 u/mL,菌株M-2达到44.41 u/mL;经菌株M-1发酵处理的菌渣蛋白质转化率达到12.79%,菌株M-2的蛋白质转化率也达到了3.65%;菌株M-1和M-2的最优菌渣转化条件分别为40 mL/250 mL装液量,菌渣添加量为10%,5%接种量,pH值 6.0,30 ℃,摇床转数160 r/min培养168 h; 100 mL/250 mL装液量,菌渣添加量为5%,接种量为9%,pH值6.5,30 ℃,摇床转数160 r/min,培养144 h。

关键词: 蛋白酶, 土霉素菌渣, 接种量, 酶活, 转化率

Abstract: This paper selected two strains of terramycin resistant mold M-1 and M-2 obtained from the compost of terramycin producing bacteria residues. The acid, alkali and terramycin tolerance of the two strains was studied. The terramycin producing slag was used as the main medium component, the protease production capacity of the two strains along with conversion capacity of the slag producing bacteria of the active ingredient was investigated. The results showed that M-1 and M-2 both had good growth at pH 3 to 7. The acid resistance of mold M-1 was better than that of strain M-2. There was no obvious inhibitory effect on the growth of the two strains, when the concentration of terramycin was below 1800 u/mL. When the strains were cultured with 5% bacterial residue suspension medium, the two strains displayed good protease production characteristics. Under the optimal culture conditions, the protease production activity of M-1 reached to 99.33 u/mL, and M-2 reached to 44.41 u/mL. The optimal bacteria residue transformation conditions for strains M-1 and M-2 were 40 mL/250 mL liquid volume, 10% bacterial residue addition, 5% inoculum volume, pH 6.0, 30 ℃, shaker rotation cultivate at 160r/min for 168 h; and 100 mL/250 mL for filling, add 5% of bacterial residue, 9% of inoculum, pH 6.5, 30 ℃ shaker at 160 r/min for 144 hours, respectively.

Key words: protease, terramycin bacteria residue, inoculum, enzyme activity, conversion

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