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中国精品科技期刊2020
肖彦骏, 曾诚, 马毛毛, 曾哲灵, 余平, 钟卫民. 用于水酶法提取中碳链油脂菌株的筛选与鉴定[J]. 食品工业科技, 2015, (22): 173-178. DOI: 10.13386/j.issn1002-0306.2015.22.028
引用本文: 肖彦骏, 曾诚, 马毛毛, 曾哲灵, 余平, 钟卫民. 用于水酶法提取中碳链油脂菌株的筛选与鉴定[J]. 食品工业科技, 2015, (22): 173-178. DOI: 10.13386/j.issn1002-0306.2015.22.028
XIAO Yan-jun, ZENG Chen, MA Mao-mao, ZENG Zhe-ling, YU Ping, ZHONG Wei-min. Screening and identification of strains for aqueous enzymatic extraction of medium-chain triglycerides[J]. Science and Technology of Food Industry, 2015, (22): 173-178. DOI: 10.13386/j.issn1002-0306.2015.22.028
Citation: XIAO Yan-jun, ZENG Chen, MA Mao-mao, ZENG Zhe-ling, YU Ping, ZHONG Wei-min. Screening and identification of strains for aqueous enzymatic extraction of medium-chain triglycerides[J]. Science and Technology of Food Industry, 2015, (22): 173-178. DOI: 10.13386/j.issn1002-0306.2015.22.028

用于水酶法提取中碳链油脂菌株的筛选与鉴定

Screening and identification of strains for aqueous enzymatic extraction of medium-chain triglycerides

  • 摘要: 筛选和应用产中性蛋白酶能力强、产脂肪酶能力很弱的耐中碳链脂肪酸型菌株,是提高水酶法提取樟树籽仁油产品得率及质量的关键。使用樟树籽仁粕粉平板富集,脱脂奶平板法、油脂平板法初筛,福林酚法、樟树籽仁培养基摇瓶复筛等方法,自樟树籽仁油生产废渣中筛选出产中性蛋白酶活力达4536.5 U/m L、产脂肪酶活力只有0.088 U/m L、适用于水酶法提取樟树籽仁油等中碳链油脂的菌株Z16。经过形态学、生理生化特征及16S r DNA分子生物学鉴定,确定菌株Z16为解淀粉芽孢杆菌(Bacillus amyloliquefaciens)。解淀粉芽孢杆菌Z16所产中性蛋白酶在50℃温度下的酶活力最高,Mn2+对其有明显的激活作用,其适宜酶解温度为4045℃、适宜酶解p H为7.0。 

     

    Abstract: Strains which had ability of higher neutral protease and lower lipase production,resistance to mediumchain fatty acids,was the key to improve yield and quality of camphor tree seed kernel oil by aqueous enzymatic extraction technology. Strain Z16 was isolated from waste residue in camphor tree seed kernel oil by screening methods(camphor tree seed kernel plate for enrichment,skim milk and oil medium plate for primary screening,Folin phenol and camphor tree seed kernel oil medium shaking for re-screening). The results showed that neutral protease and lipase production capability of Z16 were 4536.5 U/m L and 0.088 U/m L, respectively.Z16 was identified as Bacillus amyloliquefaciens by morphological, physiological and 16 S r DNA. Bacillus amyloliquefaciens had maximum neutral protease activity at 50 ℃,and was activated by Mn2 +. The optimum temperature and p H for neutral protease were 40~45 ℃ and 7.0,respectively.

     

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