摘要
为探讨酸性电解水(acidic electrolyzed water,AEW)冰对水产品的保鲜效果,以小黄鱼为对象,研究小黄鱼贮藏7 d过程中酶活力及微生物菌落总数的变化。结果表明,AEW冰抑制酸性磷酸酶、组织蛋白酶B活性的效果不明显,但对组织蛋白酶D、脂肪酶活性有显著的抑制效果(P<0.05);传统平板计数以及聚合酶链式反应-变性梯度凝胶电泳结果显示,AEW冰能抑制鱼体上腐败微生物的生长,且最大减少量可达0.34(lg(CFU/g))。因此,AEW冰技术作为一种新型高效杀菌保鲜技术,具有广阔的应用前景,相比于自来水冰更加有利于水产品的贮藏保鲜。
Acidic electrolyzed water(AEW)ice has been developed in recent years as a new food preservation technology.To investigate the effect of electrolyzed water ice on preserving the quality of small yellow croaker,changes in enzymeactivities and total viable bacterial counts were assayed periodically during seven days of storage.The results showed thatcompared with traditional tap water(TW)ice,AEW ice displayed inhibitory activity(P<0.05)toward cathepsin D and lipase,although it did not present positive effects on inhibiting acid phosphatase and cathepsin B.Conventional plate count enumerationand polymerase chain reaction-denatured gradient gel electrophoresis(PCR-DGGE)indicated that AEW ice had the capability ofinhibiting the growth of bacteria on raw fish,and the maximum reduction in bacterial population reached0.34(lg(CFU/g))on the7th day.Therefore,AEW ice has a broad application prospect and can be more useful than TW ice for preserving seafood.
作者
姚鑫
赵爱静
杜苏萍
孙晓红
潘迎捷
赵勇
YAO Xin;ZHAO Aijing;DU Suping;SUN Xiaohong;PAN Yingjie;ZHAO Yong(College of Food Science and Technology, Shanghai Ocean University, Shanghai 201306, China;Shanghai Engineering Research Center of Aquatic-Product Processing & Preservation, Shanghai 201306, China;Laboratory of Quality & Safety Risk Assessment for Aquatic Product on Storage and Preservation (Shanghai), Ministry of Agriculture, Shanghai 201306, China)
出处
《食品科学》
EI
CAS
CSCD
北大核心
2017年第13期244-250,共7页
Food Science
基金
国家自然科学基金面上项目(31271870)
上海市科委科研计划项目(14DZ1205100
14320502100)
上海市科技兴农重点攻关项目(沪农科攻字2014第3-5号
2015第4-8号)
上海水产品加工及贮藏工程技术研究中心项目(11DZ2280300)
关键词
酸性电解水冰
小黄鱼
酶活性
聚合酶链式反应-变性梯度凝胶电泳
acidic electrolyzed water (AEW) ice
small yellow croaker
enzyme activity
polymerase chain reactiondenatured gradient gel electrophoresis (PCR-DGGE)