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产黑芥子酶乳酸菌的筛选与鉴定及产酶条件的优化

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为了筛选产黑芥子酶的乳酸菌,利用氯化钯检测法测定黑芥子酶活力,从39株植物源乳酸菌中筛选产黑芥子酶菌株,通过形态特性、生理生化试验结合16S rDNA序列分析进行菌株鉴定,采用单因素试验和响应面法优化了菌株产酶条件.结果显示:3株编号分别为B244、161和602的乳酸菌能有效降解生长环境中硫代葡萄糖苷,经鉴定B244为戊糖片球菌,161和602菌株均为发酵粘液乳杆菌;戊糖片球菌(B244)具有较强的产黑芥子酶能力,在最优产酶条件(在LB培养基中添加4.2 mmol/L硫代葡萄糖苷,调整蛋白胨质量浓度至14.3 g/L,初始pH为6.9,于40℃培养16 h)下黑芥子酶活力达117.2 U/L,较优化前(76.65 U/L)提升52.9%.
Screening and identification of myrosinase-producing lactic acid bacteria and optimization of enzyme production conditions
In order to screen myrosinase-producing lactic acid bacteria,palladium chloride assay was used to determine the myrosinase enzyme activity,and the myrosinase-producing strains were screened from 39 strains of plant-derived lactic acid bacteria.The screened strains were identified by morphological characteristics,physiological and biochemical experiments in combination with 16S rDNA sequence analysis,and the enzyme-producing conditions of the strains were optimized by using the single-factor experiment and response surface method.The results showed that three strains of lactic acid bacteria(named as B244,161 and 602,respectively)could effectively degrade glucosinolates in the growth environment.Strain B244 was identified as Pediococcus pentosaceus,and 161 and 602 were both identified as Limosilactobacillus fermentum.Pediococcus pentosaceus had a strong ability to produce myrosinase,and the optimal culture conditions for the myrosinase production were as follows:4.2 mmol/L glucosinolates was added to LB medium,the mass concentration of peptones was adjusted to 14.3 g/L with the initial pH of 6.9 and incubation time of 16 h at 40℃.The myrosinase activity of B244 under the optimized condition reached 117.2 U/L,which was 52.9%higher than that(76.65 U/L)before optimization.

lactic acid bacteriamyrosinaseglucosinolatesoptimization of enzyme producingresponse surface method

杨嘉琪、赵玲艳、邓雪盈、邓放明

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湖南农业大学食品科学与技术学院,湖南 长沙 410128

湖南省产商品质量检验研究院,湖南 长沙 410007

乳酸菌 黑芥子酶 硫代葡萄糖苷 产酶条件优化 响应面法

2024

湖南农业大学学报(自然科学版)
湖南农业大学

湖南农业大学学报(自然科学版)

CSTPCD北大核心
影响因子:0.868
ISSN:1007-1032
年,卷(期):2024.50(6)