摘要
通过间苯三酚-冰醋酸法测定10种小麦及其麦芽的阿拉伯木聚糖含量、DNS法测定其木聚糖酶酶活,反应在间苯三酚-冰醋酸法和DNS法的最适反应条件下进行。结果表明:间苯三酚-冰醋酸法的最适条件是反应液用量10mL、反应20min,冷却后30min内基本稳定(P>0.05)。DNS反应最适条件为反应液用量3mL、反应15min,反应完成后35min内基本稳定(P>0.05)。8、9、10号小麦中碱溶性阿拉伯木聚糖含量最低(P>0.05),分别为0.5811±0.0127%、0.6605±0.0620%和0.6603±0.0301%;9、10号麦芽中碱溶性阿拉伯木聚糖最低(P>0.05),含量分别为0.9746±0.0085%和0.7797±0.0508%。4、8、10号小麦中水溶性阿拉伯木聚糖含量最低(P>0.05),分别为0.5423±0.0645%、0.4681±0.0127%和0.3828±0.0403%;而在麦芽中,7、8号品种最低(P>0.05),含量为0.3362±0.0518%和0.2429±0.0467%。小麦发芽后,大部分品种碱溶性阿拉伯木聚糖含量升高,增大最多的是4、7、8号品种(P>0.05),只有3号品种略微减少;水溶性阿拉伯木聚糖含量都降低。小麦发芽后木聚糖酶酶活均增大,小麦的酶活都在60.00~75.00IU/g之间,而在麦芽中各个品种间的差异不显著(P>0.05),都在100.00~120.00IU/mL之间。
The contents of arabinoxylans of 10 cultivars of wheat and their malts were determined using the method of phloroglucin-glacier acetic acid,and their xylanase activities were determined using the way of DNS under the optimal conditions,respectively.The results show that the optimal determination condition of arabinoxylans was 10mL phloroglucin-glacier acetic acid reagent,react time 20min,and within 30min after cooled the reaction product was stable(P0.05).Moreover,the optimal determination conditions of xylanase activities were as follows:3mL DNS,react time 15min,and within 35min the reaction product was stable(P0.05).In addition,the No.8,No.9 and No.10 of wheat had the lowest contents of AEAX,which were 0.5811±0.0127%,0.6605±0.0620% and 0.6603±0.0301%,respectively(P0.05);the No.9 and No.10 of wheat malts had the lowest content of AEAX,which were 0.9746±0.0085% and 0.7797±0.0508% respectively(P0.05).For content of WEAX,the No.4,No.8 and No.10 of wheats(P0.05) and the No.7 and No.8 of wheat malts(P0.05) had the lowest,which were 0.5423±0.0645%,0.4681±0.0127%,0.3828±0.0403%,0.3362±0.0518% and 0.2429±0.0467% severally.After germination,the content of AEAX in most wheats was raised except for the No.3,in which the increase of the No.4,No.7 and No.8 was maximum(P0.05);all the contents of WEAX were declined,and all the activities of xylanase were raised.In the wheats researched,the xylanase activities were between 0.6 and 0.8 IU/mL,and 0.9-1IU/mL after malting(P0.05).
出处
《酿酒》
CAS
2010年第3期56-60,共5页
Liquor Making