An extension of Bernstein-Bézier surface over the triangular domain
来自乳杆菌GG的益生化合物及其用途[发明专利]
![来自乳杆菌GG的益生化合物及其用途[发明专利]](https://img.taocdn.com/s3/m/72bb10254028915f814dc26c.png)
专利名称:来自乳杆菌GG的益生化合物及其用途专利类型:发明专利
发明人:E·B·常,E·O·彭托夫
申请号:CN200580019583.1
申请日:20050420
公开号:CN1997748A
公开日:
20070711
专利内容由知识产权出版社提供
摘要:本发明提供了用于治疗炎性病症例如炎性肠病(IBD)的方法和组合物。
使用不含细菌的、从益生菌衍生的化合物而不用活细菌提供了优于使用活细菌的安全性优点。
此外,已显示分离的化合物的临床功效比益生菌更一致,后者依赖于建立和维持细菌定殖的能力。
申请人:芝加哥大学
地址:美国伊利诺斯州
国籍:US
代理机构:中国国际贸易促进委员会专利商标事务所
代理人:陈轶兰
更多信息请下载全文后查看。
北美的五倍子

北美的五倍子
李勇民
【期刊名称】《贵州农学院学报》
【年(卷),期】1994(013)001
【摘要】在亚洲和北美大陆同时存在着倍蚜—盐肤木—藓类生物群落。
在北美有一种五倍子,形似我国的倍蛋,其倍蚜虫为美国倍蚜MelaphisrhoisFitch,它的生活史与中国倍蚜虫几乎相似。
【总页数】4页(P24-27)
【作者】李勇民
【作者单位】无
【正文语种】中文
【中图分类】S759.73
【相关文献】
1.北美自贸协定的实施对北美自贸区区内及中国矿产资源供应的影响分析 [J], 王娟;柳群义;樊礼军;姜孟源;岳俊鹏
2.五倍子及五倍子倍花中油脂的提取工艺研究 [J], 龚力民;张楚晗;汪兰;卓海燕;王文茂;汤先赤;汤赫;李顺祥
3.开眼界,拓思路,北美涂料商务考察开启——中国涂料北美商务考察团及中国涂料工业协会G20游学团商务考察纪实 [J], 赵中国;丁艳梅
4.不同种源北美乔柏和北美香柏幼苗叶挥发性成分的比较 [J], 倪妍妍;肖文发;刘建锋;张玉婷;胡军
5.梅贻琦与中国科学社北美分社的重组(1930-1931)——兼论中国科学社北美分社的兴衰 [J], 郭洋
因版权原因,仅展示原文概要,查看原文内容请购买。
微生物名人堂John E. Walker

微生物名人堂John E. WalkerJohn E. Walker AutobiographyI was born in Halifax , Yorkshire on January 7th, 1941 to Thomas Ernest Walker and Elsie Walker (ne Lawton ). My father was a stone mason, and a talented amateur pianist and vocalist. I was brought up with my two younger sisters, Judith and Jennifer, in a rural environment overlooking the Calder valley near Elland, and then in Rastrick. I received an academic education at Rastrick Grammar School , specializing in Physical Sciences and Mathematics in the last three years. I was a keen sportsman, and became school captain in soccer and cricket. In 1960, I went to St. Catherine's College, Oxford , and received the B.A. degree in Chemistry in 1964.In 1965, I began research on peptide antibiotics with E. P. Abraham in the Sir Willian Dunn School of Pathology, Oxford , and was awarded the D. Phil. degree in 1969. During this period, I became aware of the spectacular developments made in Cambridge in the 1950s and early 1960s in Molecular Biology through a series of programmes on BBC television given by John Kendrew, and published in 1966under the title The Thread of Life. These programmes made a lasting impression on me, and made me want to know more about the subject. Two books, Molecular Biology of the Gene by J. D. Watson, first published in 1965, and William Hayes' Bacterial Genetics helped to assuage my appetite for more information. My knowledge of this new field was extended by a series of exciting lectures for graduate students on protein structure given in 1966 by David Phillips, the new Professor of Molecular Biophysics at Oxford . Another series of lectures given by Henry Harris, the Professor of Pathology and published in book form undThen followed a period of five years working abroad, from 1969-1971, first at The School of Pharmacy at theUniversity of Wisconsin, and then from 1971-1974 in France, supported by Fellowships from NATO and EMBO, first at the CNRS at Gif-sur-Yvette and then at the Institut Pasteur.Just before Easter in 1974, I attended a research workshop in Cambridge entitled Sequence Analysis of Proteins. It was sponsored by EMBO (The European Molecular Biology Organization), and organised by Ieuan Harris fromthe Medical Research Council's Laboratory of Molecular Biology (LMB) and by Richard Perham from the Cambridge University Department of Biochemistry. At the associated banquet, I found myself sitting next to someone that I had not met previously, who turned out to be Fred Sanger. In the course of our conversation, he asked if I had thought about coming back to work in England . I jumped at the suggestion, and with some trepidation, approached Ieuan Harris about the possibility of my joining his group. After discussions with Fred Sanger, it was agreed that I could come to the Protein and Nucleic Acid Chemistry (PNAC) Division at the LMB for three months from June 1974. More than 23 years later, I am still there.It goes without saying that this encounter with Fred Sanger and Ieuan Harris transformed my scientific career. In 1974, the LMB was infused throughout its three Divisions with a spirit of enthusiasm and excitement for research in molecular biology led by Max Perutz (the Chairman of the Laboratory), Fred Sanger, Aaron Klug, Francis Crick, Sidney Brenner, Hugh Huxley, John Smith and Csar Milstein, which was coupled with extraordinary success. For example, alongthe corridor from my laboratory Fred was inventing his methods for sequencing DNA, immediately across the corridor Csar Milstein and Georges Kouml;hler were inventing monoclonal antibodies, and elsewhere in the building, Francis Crick and Aaron Klug and their colleagues were revealing the structures of chromatin and transfer RNA.Fred's new DNA sequencing methods were applied first to the related bacteriophages fX174 and G4, and then to DNA from human and bovine mitochondria. I analyzed the sequences of the proteins from G4 and from mitochondria uIn 1978, I decided to apply protein chemical methods to membrane proteins, since this seemed to be both a challenging and important area. Therefore, in search of a suitable topic, I read the literature extensively. The enzymes of oxidative phosphorylation from the inner membranes of mitochondria were known to be large membrane bound multi-subunit complexes, but despite their importance, they had been studied hardly at all from a structural point of view. Therefore, the same year, I began a structural study of the ATP synthase from bovine heart mitochondriaand from eubacteria. These studies resulted eventually in acomplete sequence analysis of the complex from several species, and in the atomic resolution structure of the F catalytic domain of the enzyme from bovine mitochondria, giving new insights into how ATP is made in the biological world. Michael Runswick has worked closely with me throughout this period, and has made contributions to all aspects of our studies.In 1959, I received the A. T. Clay Gold Medal. I was awarded the Johnson Foundation Prize by the University of Pennsylvania in 1994, in 1996, the CIBA Medal and Prize of the Biochemical Society, and The Peter Mitchell Medal of the European Bioenergetics Congress, and in 1997 The Gaetano Quagliariello Prize for Research in Mitochondria by the University of Bari, Italy. In 1995, I was elected a Fellow of the Royal Society. In 1997, I was made a Fellow of Sidney Sussex College, Cambridge and became an Honorary Fellow of St. Catherine's College, Oxford .I married Christina Westcott in 1963. We have two daughters, Esther, aged 21 and Miriam, aged 19. At present, both of them are university students, studying Geographyand English, respectively, at Nottingham-Trent and Leeds Universities .From Les Prix Nobel 1997.。
Method for the preparation of a protein by yeasts

专利名称:Method for the preparation of a protein by yeasts using an inducible system, vectorsand corresponding transformed strains发明人:Pierre H. Chambon,Daniel Metzger,JohnWhite申请号:US08/453888申请日:19950530公开号:US05817503A公开日:19981006专利内容由知识产权出版社提供摘要:The present invention relates to a method for the preparation of a protein by yeasts, according to which:yeast cells which contain the following are cultured:a DNA sequence coding for the protein under the control of elements providing for its expression in yeasts, the elements comprising a transcription control sequence which is inducible by a complex formed by a receptor and a ligand,a DNA sequence which is functional in yeast, coding for the receptor, the receptor comprising two essential portions, one of which recognizes the ligand so as to form a complex with the ligand and the other binds to the said transcription control sequence; the portion of the receptor which recognizes the ligand is of higher eukaryotic origin, and the ligand is not necessary for the culturing of the cells but is capable of entering the cells when added to the culture medium,the ligand is added to the culture medium at an appropriate time point for induction,the synthesized protein is recovered.申请人:CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (C.N.R.S.)代理机构:Cushman Darby & Cushman IP Group of Pillsbury Madison & Sutro LLP 更多信息请下载全文后查看。
杏鲍菇废弃菌渣中D-氨基葡萄糖盐酸盐的制备工艺及生物学活性分析

张倩如,吴启赐,薛钰,等. 杏鲍菇废弃菌渣中D-氨基葡萄糖盐酸盐的制备工艺及生物学活性分析[J]. 食品工业科技,2023,44(17):263−271. doi: 10.13386/j.issn1002-0306.2022110139ZHANG Qianru, WU Qici, XUE Yu, et al. Preparation and Biological Activity of D-Glucosamine Hydrochloride from the Waste Residues of Pleurotus eryngii [J]. Science and Technology of Food Industry, 2023, 44(17): 263−271. (in Chinese with English abstract).doi: 10.13386/j.issn1002-0306.2022110139· 工艺技术 ·杏鲍菇废弃菌渣中D-氨基葡萄糖盐酸盐的制备工艺及生物学活性分析张倩如1,吴启赐1, *,薛 钰1,林志超1,黄家福1,吕昊坤1,彭 伟1,潘裕添1,林进妹2,*(1.闽南师范大学菌物产业福建省高校工程研究中心,福建漳州 363000;2.闽南师范大学化学化工与环境学院,福建漳州 363000)摘 要:本文以杏鲍菇废弃菌渣为原料,探究了D-氨基葡萄糖盐酸盐(D-glucosamine hydrochloride ,GAH )的制备工艺、液相-质谱(HPLC-MS )、红外光谱、理化指标及其对斑马鱼胚胎发育的影响。
采用单因素和响应面优化试验,获得盐酸水解制备GAH 的最佳条件:盐酸浓度31%,水解时间4 h ,水解温度82 ℃,液固比5 mL/g ,此时GAH 得率可达23.61%。
液相-质谱、红外光谱和理化指标分析显示,GAH 纯化样品纯度是标准品的101.9%,质谱和红外光谱图与标准品一致,各项指标均符合甚至优于美国药典43-国家处方集38(USP43-NF38)的质量标准,砷含量仅0.21 μg/g 。
Method of producing a hollow turbine blade and mul

地址:FR
国籍:FR
更多信息请下载全文后查看
专利内容由知识产权出版社提供
专利名称:Method of producing a hollow turbine blade and multiple effect furnace-press for carrying out method
发明人:BERGUE, JEAN-PIERRE SERGES,BICHON, MATHIEU PHILIPPE ALBERT,LACUISSE, JEAN-FRANCOIS GEORGES JULIEN,LORIEUX, ALAIN GEORGES HENRI
申请号:EP 974 01325.2 申请日:19970612 公开号:EP 081264 9B 1 公开日:20020731
摘要:A procedure for manufacturing a hollow turbine blade, especially a large-chord fan rotor blade, uses computer-assisted design to simulate the components of the blade, followed by forging and machining the primary components, depositing diffusion barriers, assembling and inflating. The procedure also includes an operation for isothermic shaping of the titanium alloy blank (9) under pressure and at a temperature of 700 - 940 degrees C. The operation uses two or more dies (46), a blank holder (45) and a matrix (21), ensuring a controlled deformation speed so that the fibres of the material are distributed evenly on either side of its lengthwise axis.
SPE 168243 英语翻译

SPE 168243
在高温井内的电缆牵引器;一个当地的故事集
马特人民,提姆-哈米尔,奥利维尔Alferez和加里将,华大®
版权所有2014,石油工程师学会
本文是2014 年 3 月25-26,在美国得克萨斯州准备在SPE/连续性油管& 井干预会议&在林地举行展览的演示文稿。
本论文由SPE程序委员会选择来表示在以下的评论信息中一个作者(S)提出的摘要。
本文的内容未被由石油工程师学会查看,也没有被作者(S)修改。
材料不一定代表其中任一管理人员,或成员在石油工程师协会的职位。
没有石油工程师协会的书面同意,禁止电子复制,分发,或储存的任何部分的文章用于商业目的,印刷复制许可限制不超过摘要的300个字;包含摘要必须被 SPE版权承认。
摘要
德克萨斯和路易斯安那通常不被认为是极端的环境,但海恩斯维尔和鹰福特有一些热点和深地区正在开发中。
高温环境要求专业的,强有力的干预工具设计能够承受长时间的极端高温。
Mixture of catechins or rather polyphenols extract

专利名称:Mixture of catechins or rather polyphenols extracted from chinese greentea or othervegetables for the prevention of prostatecancer and for the treatment of prostatehypertrophy (bph)发明人:BETTUZZI, SAVERIO,CORTI,ARNALDO,CORVETTA, SERGIO申请号:IB2005002107申请日:20050721公开号:WO2006013420B1公开日:20060608专利内容由知识产权出版社提供摘要:The formulation and modality of use of a pharmaceutical preparation having the properties described below is described. This preparation is a product comprising a mixture of catechins or polyphenols extracted from chinese green tea or other vegetables that has proven to be efficacious in the chemical prevention of prostate cancer in a clinical pilot study when administered in adequate systemic dosage without the aid of other conventional drugs or remedies and without adverse effects in a group of subjects at risk of development of the illness. The same reduction of the preparation proved efficacious in symptomatology of benign prostate hypertrophy and especially as concerns the difficulty of urination when administered in adequate dosage systemically without the aid of other drugs or conventional remedies and without adverse effects in the patients subject of the study.申请人:GENPROFILER S.R.L.,BETTUZZI, SAVERIO,CORTI, ARNALDO,CORVETTA, SERGIO更多信息请下载全文后查看。