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作 者:王凤荣[1] 乔长晟[1] 江建梅[1] 钟堃[1] 李鹏举[1] 贾士儒[1]
机构地区:[1]天津市工业微生物重点实验室,工业微生物教育部重点实验室,天津科技大学,天津300457
出 处:《食品工业科技》2010年第6期347-349,352,共4页Science and Technology of Food Industry
基 金:天津市高等学校科技发展基金(ZD200703)
摘 要:应用α-2,7-萘二酚法和酶试剂盒法分别对L-苹果酸标准品和出芽短梗霉(Aureobasidium pullulans)发酵液中的聚苹果酸进行检测,比较二者的差异,并研究了酸解过程对两种检测方法的影响。结果表明:检测L-苹果酸标准品,α-2,7-萘二酚法回收率为99.58%~100.1%,相对标准偏差为0.71%~0.95%,酶试剂盒法回收率为99.6%~100.22%,相对标准偏差为0.55%~0.6%,经统计学分析两种方法的准确度和精密度无显著性差异;检测发酵液中聚苹果酸,α-2,7-萘二酚法相对标准偏差为2.49%~3.61%,酶试剂盒法相对标准偏差为0.81%~1.18%,经统计学分析两种方法的准确度和精密度无显著性差异;酸解过程对两种检测方法均无显著影响。α-2,7-hydronaphthoquinone method and L-MALATE kit method were used for L-malic acid and poly (β-L-malic acid) in culture broth produced by Aureobasidium pullulans,as well as the influence of acidolysis on the two determination methods.The results showed that the return-ratio and relative standard deviation of α-2,7- hydronaphthoquinone method were 99.58%- 100.1% and 0.71 %-0.95%, respectively, the return- ratio and relative standard deviation of L-MALATE kit method were 99.6%-100.22% and 0.55%-0.6%, respectively, there were no significant different in the accuracy and precision of the two methods.Results of determination of poly (13-L-malic acid) in culture broth by these methods were as follows: the relative standard deviation of α- 2, β- hyd ronaphthoquinone method and L- MALATE kit method was 2.49 %--3.61% and 0.81%~ 1.18 %, respectively, there were no significant different in the accuracy and precision of the two methods. Acidolysis had neither notable infhfluence on the α-2 β-hydronaphthoquinone method nor L-MALATE kit method.
关 键 词:α-2 7-茶二酚法 L-苹果酸酶试剂盒法 L-苹果酸 聚苹果酸
分 类 号:TS207.3[轻工技术与工程—食品科学]
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