不同参数对hunza品种野李粕中脂肪酶和磷脂酶溶脂活性的影响

A. Hifza
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引用次数: 0

摘要

李属Arminica。以氯仿与甲醇(2:1v/v)的混合物为溶剂,采用超声辅助提取技术对罕萨L种子进行脱脂。提取脂肪酶和磷脂酶,在400C和pH 6柠檬酸缓冲液中孵育1小时。测定了酶在不同温度(30 ~ 700c)、pH(1)、pH(3 ~ 9)和溶剂(1)、正庚烷、二异丙醚和环己烷)下的溶脂活性。10%卵磷脂乳液和橄榄油分别作为磷脂酶底物和脂肪酶底物。酶在较低温度(35 ~ 500℃)和微酸性至中性(pH 5 ~ pH 7)下表现出稳定性。用440nm吸光度法测定酶活性,并以游离脂肪酸浓度为指标。采用硬脂酸在正己烷和甲醇中不同浓度(1:1v/v)作标准曲线。本研究采用少量CaCl2的Cu-TEA试剂最大限度地提取Cu-FFA,并使空白值稳定。酶在450℃温度和6 pH条件下活性最高。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
EFFECTS OF DIFFERENT PARAMETERS ON THE LIPOLYTIC ACTIVITIES OF LIPASE AND PHOSPHOLIPASE EXTRACTED FROM PRUNUS ARMINICA MEAL OF HUNZA CULTIVAR
Prunus Arminica.L seeds of Hunza cultivar were defatted with chloroform, methanol mixture (2:1v/v) by ultrasonic assisted extraction technique. The lipase and phospholipase extracted, incubated at 400C and pH 6 in citrate buffer for 1 hour. The lipolytic activities of enzymes were measured at different temperatures i,e 30-700C , pH i,e 3-9 and solvents i,e n-heptane , Di-isopropyl ether and Cyclo hexane. 10 % emulsion of lecithin and olive oil used as the substrate for phospholipase and lipase substrates respectively. The enzymes showed stability at lower temperatures i,e 35-500C and slightly acidic to neutral i.e pH 5 to pH 7. Concentration of liberated fatty acids was the indicator of the enzymes activity which were measured by taking absorbance at 440nm. Stearic acid with different concentrations in hexane and methanol (1:1v/v) were used for the standard curve. Cu-TEA reagent with small quantity of CaCl2 was used for maximum extraction of Cu-FFA and for stable value of blanks in the present study. The enzymes showed maximum activities at 450 C temperature and 6 pH.
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