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Food‑grade expression of multicopper oxidase with improved capability in degrading biogenic amines
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作者 xiumei ni Jian Chen +1 位作者 Guocheng Du Fang Fang 《Systems Microbiology and Biomanufacturing》 2022年第2期285-295,共11页
Biogenic amines(BAs)are potential amine hazards that are detected in fermented foods and alcoholic beverages.Excessive intake of BAs may lead to allergic symptoms such as difculty in breathing,nausea,and vomiting.Degr... Biogenic amines(BAs)are potential amine hazards that are detected in fermented foods and alcoholic beverages.Excessive intake of BAs may lead to allergic symptoms such as difculty in breathing,nausea,and vomiting.Degradation of BAs by multicopper oxidase(MCO)is a promising method as it has little efect on the fermentation process,food nutrition,and favor.However,the application of MCO in food industry was restricted due to its poor catalytic properties and low productivity.In this work,food-grade expression of the Bacillus amyloliquefaciens MCO(MCOB)and its three mutants were successfully constructed in Lactococcus lactis NZ3900.The expression level of MCOB in L.lactis NZ3900 was dramatically enhanced by optimizing the cultivation conditions,and the highest expression level reached 4488.1 U/L.This was the highest expression level of food-graded MCO reported so far,to our knowledge.Interestingly,the optimal reaction pH of MCOB expressed in L.lactis NZ3900 switched to 4.5,it would be more suitable for degrading BAs in food as the pH value of most fermented foods was found to be 4.5.Moreover,MCOB expressed in L.lactis NZ3900 was quite stable(with more than 80%residual activity)in the pH range of 4.0–5.5,the catalytic rate constant(kcat)and specifc activity of MCOBLS were all dramatically increased compared with that of MCOB expressed in Escherichia coli.Using histamine as the substrate,the degradation of BAs within 24 h by MCOB expressed in L.lactis NZ3900 was 69.7%higher than that expressed in E.coli.The results demonstrated the potential applications of MCOB in food industry for reduction of biogenic amines. 展开更多
关键词 Biogenic amines HISTAMINE Degradation Multicopper oxidase Food-grade expression
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融合表达过氧化氢酶提高多铜氧化酶稳定性及降解生物胺能力 被引量:1
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作者 倪秀梅 方芳 《生物工程学报》 CAS CSCD 北大核心 2021年第12期4382-4394,共13页
多铜氧化酶(Multicopper oxidase,MCO)家族中的某些酶可以通过氧化反应降解食品中的胺类危害物生物胺。然而酶在催化时因为持续被氧化可能会影响整个反应过程中MCO的活性及稳定性,使酶的催化效率和降解生物胺的能力下降。文中成功在大... 多铜氧化酶(Multicopper oxidase,MCO)家族中的某些酶可以通过氧化反应降解食品中的胺类危害物生物胺。然而酶在催化时因为持续被氧化可能会影响整个反应过程中MCO的活性及稳定性,使酶的催化效率和降解生物胺的能力下降。文中成功在大肠杆菌EscherichiacoliBL21(DE3)中构建并表达了来源于发酵乳杆菌Lactobacillus fermentum的多铜氧化酶(MCOF)与枯草芽孢杆菌过氧化氢酶(CAT)的融合酶。8种融合酶对H2O2的耐受性提高了51%–68%,融合酶CAT&MCOF在降解组胺的过程中稳定性比MCOF提高了17.3%。以2,2′-联氮-双-3-乙基苯并噻唑啉-6-磺酸(2,2′-azino-bis(3-ethylbenzothiazoline-6-sulfonicacid), ABTS)为底物时,CAT&MCOF对底物的亲和力(Km)提高了1.0倍,催化效率(kcat/Km)提高了1.7倍,摩尔比酶活提高了1.2倍,且在酸性(pH 2.5–4.5)和中高温(35–55℃)条件下的稳定性都有不同程度的提高。此外,CAT&MCOF对腐胺、尸胺和组胺的降解率分别为31.7%、36.0%和57.8%,分别比MCOF提高了132.5%,45.7%和38.9%。多铜氧化酶与过氧化氢酶融合表达提高酶催化稳定性和催化效率的策略将为通过酶的分子改造提高其应用特性提供参考。 展开更多
关键词 多铜氧化酶 生物胺 稳定性 融合表达 过氧化氢酶
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