首页 | 本学科首页   官方微博 | 高级检索  
   检索      

低温对螺旋藻可溶性蛋白和游离氨基酸外渗的影响
引用本文:栗淑媛,马华山,王俊琴,乔辰.低温对螺旋藻可溶性蛋白和游离氨基酸外渗的影响[J].西北植物学报,2005,25(6):1195-1198.
作者姓名:栗淑媛  马华山  王俊琴  乔辰
作者单位:1. 内蒙古师范大学,生命科学与技术学院,呼和浩特,010022
2. 内蒙古农业大学,农学院,呼和浩特,010019
基金项目:国家自然科学项目 No.3 9960 0 62,内蒙古自然科学基金项目 No.2 0 0 3 0 80 2 0 3 10
摘    要:以鄂尔多斯高原碱湖特有的钝顶螺旋藻S1、引进的钝顶螺旋藻S2和极大螺旋藻S3为材料,采用Folin法和茚三酮法分别测定低温下细胞外渗液中可溶性蛋白和游离氮基酸含量。结果表明:处理温度越低,时间越长,螺旋藻细胞外渗液中可溶性蛋白和游离氨基酸的含量越高。S1膜损伤程度最轻,比引进种S2、S3有较强的抗寒能力。判断低温对螺旋藻膜损伤的程度,用可溶性蛋白较游离氨基酸更接近于实际。

关 键 词:螺旋藻(节旋藻)  低温  可溶性蛋白  游离氨基酸
文章编号:1000-4025(2005)06-1195-04

Effect of Low Temperature on the Exosmosises of Soluble Protein and Free Amino Acid from Spirulina (Arthrospira)
LI Shu-yuan,MA Hua-shan,WANG Jun-qin,QIAO Chen.Effect of Low Temperature on the Exosmosises of Soluble Protein and Free Amino Acid from Spirulina (Arthrospira)[J].Acta Botanica Boreali-Occidentalia Sinica,2005,25(6):1195-1198.
Authors:LI Shu-yuan  MA Hua-shan  WANG Jun-qin  QIAO Chen
Institution:LI Shu-yuan 1,MA Hua-shan 1,WANG Jun-qin 1,QIAO Chen 2*
Abstract:Folin procedure and ninhydrin method were adopted to determine the contents of soluble proteins and free amino acids in the cellular extravasations of Spirulina (Arthrospira) platensis (S_1) only found in the natron lakes of the Ordos Plateau,introduced S. (A.) platensis (S_2) and S. (A.) maxima (S_3) .The results showed that the lower the treating temperature was and the longer the treating time lasted,the higher the contents of soluble protein and free amino acids in the cellular extravasation of Spirulina (Arthrospira) would become.S_1 suffered the least membrane damage,which indicated that it had a stronger frost resistance than S_2 and S_3.The damage of low temperature to Spirulina (Arthrospira) membrane that was evaluated according to soluble proteins would be closer to its ;ractical damage than that according to free amino acids.
Keywords:Spirulina (Arthrospira)  low temperature  soluble protein  free amino acid
本文献已被 CNKI 维普 万方数据 等数据库收录!
点击此处可从《西北植物学报》浏览原始摘要信息
点击此处可从《西北植物学报》下载免费的PDF全文
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号