期刊文献+
共找到6篇文章
< 1 >
每页显示 20 50 100
海栖热袍杆菌来源的极耐热碱性果胶裂解酶的表达、纯化及定性 被引量:10
1
作者 李平 景庆庆 邵蔚蓝 《生物工程学报》 CAS CSCD 北大核心 2009年第2期223-229,共7页
将来源于极端嗜热菌属海栖热袍杆菌Thermotoga maritima MSB8的编码碱性果胶裂解酶的结构基因pelA与新型热激质粒pHsh连接,得到重组质粒pHsh-pelA,运用mRNA二级结构预测软件对pHsh-pelA的翻译起始区的二级结构进行优化,得到了具有最佳m... 将来源于极端嗜热菌属海栖热袍杆菌Thermotoga maritima MSB8的编码碱性果胶裂解酶的结构基因pelA与新型热激质粒pHsh连接,得到重组质粒pHsh-pelA,运用mRNA二级结构预测软件对pHsh-pelA的翻译起始区的二级结构进行优化,得到了具有最佳mRNA二级结构及自由能的质粒pHsh-pelC。将重组质粒pHsh-pelC转入大肠杆菌JM109(DE3)进行表达,得到了一种极耐热性碱性果胶裂解酶(PelC)。对重组酶的酶学性质研究发现,该酶的最适反应温度为90℃,最适反应pH为8.5,在pH 8.2-9.8之间酶活力稳定,95℃酶活半衰期为2 h,并且该酶依赖Ca^2+作为活性离子。在工业生产常用温度60℃下,该酶能够长时间保持稳定,并具有较高的酶活力。以多聚半乳糖醛酸(PGA)为底物时,其动力学参数Km值为0.11 mmol/L,Vmax值为327 U/mg。SDS-PAGE结果显示该重组酶的分子量为43 kD,与理论值相符。基于热激载体pHsh的重组表达系统具有诱导表达简便、诱导方式廉价的优点,且重组酶热稳定性非常好,这对该酶的大规模发酵应用具有重要意义。 展开更多
关键词 耐热碱性果胶裂解酶 纯化定性 热激载体
原文传递
Purification and Stability of an Antithrombus Enzyme from Bacillus subtilis
2
作者 关怡新 姚善泾 +1 位作者 俞丽华 梅乐和 《Chinese Journal of Chemical Engineering》 SCIE EI CAS CSCD 2004年第5期707-710,共4页
An antithrombus enzyme (ATE) was precipitated by (NH4)2SO4 or ethanol from supernatant of Bacillus subtilis culture broth then purified using ion exchange chromatography on CM-sepharose fast flow. The effects of ionic... An antithrombus enzyme (ATE) was precipitated by (NH4)2SO4 or ethanol from supernatant of Bacillus subtilis culture broth then purified using ion exchange chromatography on CM-sepharose fast flow. The effects of ionic strength and pH value on protein adsorption, the gradient elution at different flow rates and step elution were examined respectively. The recovery yield of the optimised process was 74.5% with a purification factor 8.1. The ATE molecular weight was estimated as 30ku by SDS-PAGE. The experimental results showed that the enzyme was stable in the range of pH 7 to pH11, and temperature 25℃ to 37℃. 展开更多
关键词 antithrombus enzyme PURIFICATION ion exchange chromatography ADSORPTION STABILITY
下载PDF
Perspectives in application of biosensors for the modernization of traditional Chinese medicine
3
作者 Qiang Chen Hong-Cai Shang +1 位作者 Bing-Kai Han Jun Jiao 《TMR Modern Herbal Medicine》 2018年第1期39-46,共8页
Biosensor is an instrument which is sensitive to biological material and converts its concentration into electrical signals.Organisms such as enzymes, antibodies, tissues, cells and so on can selectively identify spec... Biosensor is an instrument which is sensitive to biological material and converts its concentration into electrical signals.Organisms such as enzymes, antibodies, tissues, cells and so on can selectively identify specific substances. Thesemolecular recognition functions can be combined with the target, such as the binding of antibodies and antigens, and thebinding of enzymes to the substrate through the recognition process. Biosensor has the advantages of high specificity,high sensitivity, fast reaction speed, low cost and easy operation. It has wide application prospect in food, pharmacy,chemical industry, clinical examination, biomedicine, environmental monitoring and so on, especially as a newtechnology means, in the field of modern herbal medicine research influence. Studies have demonstrated that thebiosensing technology has been applied to, traditional Chinese medicine (TCM) targets, isolation and purification ofTCM, the mechanism of TCM, quality control of TCM, the active ingredients detection of TCM and other basicresearches. Biosensor technology has made an important contribution to the research of modern herbal medicine, and hasbecome a Hot-spot in future research. 展开更多
关键词 BIOSENSOR Traditional Chinese medicine PURIFICATION Active compound identification MECHANISM Qualitycontrol
下载PDF
Comparison of methods of purification and identification of Verticillium dahliae toxins
4
作者 JIA Zhi-qi SHI Fu-mei YUAN Hai-yong HOU Yan-yan LI Ying-zhang 《Journal of Life Sciences》 2007年第1期67-72,81,共7页
The complexes excreted by VerticiUium dahliae are phytotoxins, which are responsible for most of the symptoms associated with Verticillium wilt disease. Verticillium dahliae toxins (VD-toxins) can be purified by dif... The complexes excreted by VerticiUium dahliae are phytotoxins, which are responsible for most of the symptoms associated with Verticillium wilt disease. Verticillium dahliae toxins (VD-toxins) can be purified by different methods. In the present study, we reported a simpler, more effective method to purify VD-toxins. The supematant of V. dahliae culture was frozen, lyophilized and dialyzed by 1 kDa Dialysis Membranes (MWCO). We also partially identified the characteristics of the purified VD-toxins. The results showed that the components of VD-toxins include glycoprotein within 35.8-83.2 kDa. The phytotoxic activity of VD-toxins was remained after VD-toxins were pretreated by high temperature, Concanavalin-A, and proteinase E, respectively. These data suggest that VD-toxins are heat-stable, and the protein fraction and glycosyl are both important contributors to the phytotoxic activity. VD-toxins purified effectively from the culture filtrates of V. dahliae may help in further understanding the mechanisms of interactions between V. dahliae and plants. 展开更多
关键词 GLYCOPROTEIN PHYTOTOXICITY PURIFICATION Verticillium dahliae toxins
下载PDF
罗非鱼肝脏中辅酶Q_(10)的研究 被引量:2
5
作者 吴燕燕 郝志明 +3 位作者 李来好 岑剑伟 郝淑贤 陈胜军 《中国食品学报》 EI CAS CSCD 2006年第1期195-199,共5页
辅酶Q10是一种重要的类维生素有机物,是促进生物氧化的酶类生化药物。通过L16(45)正交实验,研究皂化法提取辅酶Q10的工艺条件;用硅胶柱层析及制备硅胶板分离纯化;用薄层色谱、紫外光谱对提纯样品进行定性及定量分析。结果表明:皂化法提... 辅酶Q10是一种重要的类维生素有机物,是促进生物氧化的酶类生化药物。通过L16(45)正交实验,研究皂化法提取辅酶Q10的工艺条件;用硅胶柱层析及制备硅胶板分离纯化;用薄层色谱、紫外光谱对提纯样品进行定性及定量分析。结果表明:皂化法提取罗非鱼肝脏辅酶Q10的最佳工艺条件是:皂化温度70℃、皂化时间30min、萃取4次。经硅胶柱层析,每100g罗非鱼肝脏可以提取纯化辅酶Q103.39mg。 展开更多
关键词 辅酶Q10提取纯化定量定性分析
原文传递
Purification and characterization of CHpro1, a thermotolerant, alkali-stable and oxidation-resisting protease of Chumathang hotspring
6
作者 Reena Singh Chirag Chopra +3 位作者 Vishnu Kumar Gupta Bashir Akhlaq Vijeshwar Verma Shafaq Rasool 《Science Bulletin》 SCIE EI CAS CSCD 2015年第14期1252-1260,共9页
Metagenomic approaches are recently used for searching novel open reading frames (ORFs) coding enzymes employed in pharmaceutical, rood industries, etc. In this study, a metagenornic library was constructed from Chu... Metagenomic approaches are recently used for searching novel open reading frames (ORFs) coding enzymes employed in pharmaceutical, rood industries, etc. In this study, a metagenornic library was constructed from Chumathang hotspring sediment DNA. The library consisted of approximately 9,000 clones and was screened for protease activity. A clone exhibiting protease activity was identified and named CHprol. Sequencing of CHprol revealed that the ORF encoded a functional protein of 363 amino acids belonging to peptidase S8-S53 superfamily. CHprol shared 41% sequence similarity with a reported protease (subtilase family) and 35 % structural similarity with the crystal structure of Pro-Tk sps. of Thermococcus kodarkaenasis. In silico modeling the 3D structure of CHprol showed that it has two beta sheets, 10 alpha helices and 11 strands. Catalytic triad prediction implied CHprol to be a serine protease. The optimum temperature and pH of the purified protease were found to be 80 ℃ and 11.0, respectively. The enzyme was active at 5 % concentration of hydrogen peroxide and retained 60 % of activity at 10 % concentration. The thermotolerant, alkalophilic and oxidant stable properties of the protease make it a potential can- didate for biotechnological applications. 展开更多
关键词 Thermotolerant. Alkalophilic Oxidantstable PROTEASE Hotspring METAGENOMICS
原文传递
上一页 1 下一页 到第
使用帮助 返回顶部