生物技术
生物技術
생물기술
BIOTECHNOLOGY
2010年
1期
62-65
,共4页
张一平%华洵璐%李靖%谢骏%何义进
張一平%華洵璐%李靖%謝駿%何義進
장일평%화순로%리정%사준%하의진
麦芽根%5'-磷酸二酯酶%核苷酸%超滤%盐析
麥芽根%5'-燐痠二酯酶%覈苷痠%超濾%鹽析
맥아근%5'-린산이지매%핵감산%초려%염석
barley rootlets%5' -phosphodiesterase%5' - nucleotides%ultrafiltration%salting out
目的:获得高活力5'-磷酸二酯酶液,提高核酸RNA酶解效率.方法:采用超滤和盐析技术对从麦芽根浸提液中纯化5'-磷酸二酯酶工艺进行研究,采用单因子试验法优化酶解工艺条件.结果:浸提液依次经过5万Da超滤膜浓缩、40%饱和度硫酸铵盐析、5万Da超滤膜脱盐后,酶活力可达1 500U/ml;第1次超滤膜透过液可作为浸提液循环使用,酶活力是水浸提的1.15倍;第2次超滤膜透过液浓缩5倍后,可回收56.46%硫酸铵,浓缩母液可按1:2比例循环使用;在底物浓度5.8%、酶用量8%、反应时间2h条件下,RNA酶解率可达95%.结论:初步建立了适合工业化规模的核苷酸生产新工艺.
目的:穫得高活力5'-燐痠二酯酶液,提高覈痠RNA酶解效率.方法:採用超濾和鹽析技術對從麥芽根浸提液中純化5'-燐痠二酯酶工藝進行研究,採用單因子試驗法優化酶解工藝條件.結果:浸提液依次經過5萬Da超濾膜濃縮、40%飽和度硫痠銨鹽析、5萬Da超濾膜脫鹽後,酶活力可達1 500U/ml;第1次超濾膜透過液可作為浸提液循環使用,酶活力是水浸提的1.15倍;第2次超濾膜透過液濃縮5倍後,可迴收56.46%硫痠銨,濃縮母液可按1:2比例循環使用;在底物濃度5.8%、酶用量8%、反應時間2h條件下,RNA酶解率可達95%.結論:初步建立瞭適閤工業化規模的覈苷痠生產新工藝.
목적:획득고활력5'-린산이지매액,제고핵산RNA매해효솔.방법:채용초려화염석기술대종맥아근침제액중순화5'-린산이지매공예진행연구,채용단인자시험법우화매해공예조건.결과:침제액의차경과5만Da초려막농축、40%포화도류산안염석、5만Da초려막탈염후,매활력가체1 500U/ml;제1차초려막투과액가작위침제액순배사용,매활력시수침제적1.15배;제2차초려막투과액농축5배후,가회수56.46%류산안,농축모액가안1:2비례순배사용;재저물농도5.8%、매용량8%、반응시간2h조건하,RNA매해솔가체95%.결론:초보건립료괄합공업화규모적핵감산생산신공예.
Objective: Obtained the high activity 5' - phosphodiesterase liquid, and raised the enzymatic hydrolysis yield of RNA. Method: The purification technology and enzyme hydrolysis condition were studied by ultrafiltration, salting out technique and individual factor experiment. Result: The best technology was concentrating by 50 000 Da ultrafiltration membrane, salting out with 40% saturation (NH_4)_2SO_4 ,and desalination by 50 000 Da ultrafiltration membrane in turn, so that the liquid of 1500 U/ml activity could be obtained;the filtrate of first ultrafiltration could be reused as new extract liquid, and its enzyme activity was 1. 15 times than the water extract; the filtrate of second ultrafiltration was concentrated to l/5 volume, then 56.46% (NH_4)_2SO_4 could be harvest, and the mother liquor could be reused in the ratio of 1:2; under the condition of 5.8% RNA,8% enzyme concention,and 2 hours reaction time, the 95% enzymatic hydrolysis yield of RNA could be reached. Conclusion: The technology of this paper could be used in nucleotide manufacture on industry scale.