Sung H G, Shin H T, Ha J K, Lai H-L, Cheng K-J, Lee J H
School of Agricultural Biotechnology, College of Agriculture and Life Sciences, Seoul National University, Seoul 151-742, Republic of Korea.
Bioresour Technol. 2005 Jul;96(11):1297-303. doi: 10.1016/j.biortech.2004.10.010. Epub 2005 Jan 25.
The effects of germination temperature on the growth of barley seedlings for phytase production were studied at 15, 20 and 25 degrees C for 6-10 days. The growth rate of the barley seedlings was increased as the germination temperature was increased. The initial rate of total protein production was closely coupled to that of the barley growth, and the rate of total protein production tended to increase as the germination temperature was increased. SDS-PAGE analysis of total protein from the barley seedlings showed time-dependent appearance and disappearance of protein bands. Although no significant phytase activity was detected at zero time of germination, a significant increase in phytase activity up to 7.9-fold occurred during the first several days of germination then decreased. Phosphate production (viz. phytate degradation) in the barley seedlings occurred rapidly at the beginning of germination. However, the rate of production continued to decrease with further germination. A time lag of about 1-2 days between the rate of total protein production and that of phytase production was observed. Unlike the extent of total protein production, that of phytase production was similar irrespective of germination temperature. Partial purification of a crude enzyme extract by hydrophobic interaction chromatography resulted in two phytase fractions (PI and PII). Zymogram analysis demonstrated that PI had two bands with molecular masses of about 66 and 123 kDa while PII had one band corresponding to a molecular mass of about 96 kDa. The optimal temperature for PI was found to be 55 degrees C, while it was 50 degrees C for PII. The enzyme fraction PI had a pH optimum at 6.0, whereas the optimum pH for PII was found to be 5.0. Addition of 0.1% (v/v) Tween 80 was found to increase enzyme activity significantly (i.e., 167% for PI and 137% for PII). Phytate in cereals including barley, rice, corn and soybean degraded effectively by the treatment of the barley phytases.
研究了在15、20和25摄氏度下,发芽温度对用于植酸酶生产的大麦幼苗生长的影响,处理时间为6至10天。随着发芽温度升高,大麦幼苗的生长速率增加。总蛋白产生的初始速率与大麦生长速率紧密相关,并且随着发芽温度升高,总蛋白产生速率趋于增加。对大麦幼苗总蛋白的SDS-PAGE分析显示,蛋白条带出现和消失具有时间依赖性。尽管在发芽零时未检测到显著的植酸酶活性,但在发芽的最初几天内,植酸酶活性显著增加,最高可达7.9倍,随后下降。大麦幼苗中的磷酸盐产生(即植酸盐降解)在发芽开始时迅速发生。然而,随着进一步发芽,产生速率持续下降。观察到总蛋白产生速率和植酸酶产生速率之间存在约1至2天的时间滞后。与总蛋白产生程度不同,无论发芽温度如何,植酸酶产生程度相似。通过疏水相互作用色谱法对粗酶提取物进行部分纯化,得到两个植酸酶组分(PI和PII)。酶谱分析表明,PI有两条分子量约为66和123 kDa的条带,而PII有一条对应分子量约为96 kDa的条带。发现PI的最适温度为55摄氏度,而PII为50摄氏度。酶组分PI的最适pH为6.0,而PII的最适pH为5.0。发现添加0.1%(v/v)吐温80可显著提高酶活性(即PI提高167%,PII提高137%)。包括大麦、水稻、玉米和大豆在内的谷物中的植酸盐通过大麦植酸酶处理可有效降解。