{"title":"Interference of electromagnetic waves in dynamic metabolism.","authors":"K Huang, J Tang, Y Liu, L Xu","doi":"","DOIUrl":"","url":null,"abstract":"<p><p>Life is a continuous process of the dynamic metabolism. The influence of electromagnetic waves on the process of metabolism cannot be neglected. Here a new theory of electromagnetic interference in the dynamic metabolism of life is proposed. The statistical dynamic equations of ion and free radical in the biochemical reaction radiated by electromagnetic waves are given. The intensity of electromagnetic interference could be described with an interference factor. Good agreement can be seen between the calculated and measured results for a famous experiment of radio-frequency radiation-induced calcium ion efflux enhancement.</p>","PeriodicalId":21648,"journal":{"name":"Science in China. Series B, Chemistry, life sciences & earth sciences","volume":"38 11","pages":"1355-60"},"PeriodicalIF":0.0,"publicationDate":"1995-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"19719003","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
J Duan, J Wang, J Han, S Peng, M Zou, J Miao, C Zhao, X Ma
{"title":"Cloning, expression and purification of the ligand-binding region of human IL-6R in E. coli and its preliminary functional identification.","authors":"J Duan, J Wang, J Han, S Peng, M Zou, J Miao, C Zhao, X Ma","doi":"","DOIUrl":"","url":null,"abstract":"<p><p>The ligand-binding region of human IL-6R is taken as the target gene fragment to be cloned and expressed. With pET-3b as expressing vector, two recombinants pET-6R(B) and pET-6R(B)4 have been constructed encoding the ligand-binding region (28 kD) of hIL-6R and its dimmer (53 kD), respectively. After induction with IPTG, they produced two proteins rIL6R-28 of 28 kD and rIL6R-53 of 53 kD amounting to 50% and 30% of total bacteria proteins, respectively. The expressed products were mainly recovered as inclusion bodies. After purification and renaturation, both of them were capable of augmenting the growth-stimulating effect of IL-6 on 7TD1 cells, an IL-6 dependent cell line. The result of ELISA also revealed that both rIL6R-28 and rIL6R-53 had the obvious ligand-binding activity.</p>","PeriodicalId":21648,"journal":{"name":"Science in China. Series B, Chemistry, life sciences & earth sciences","volume":"38 11","pages":"1321-31"},"PeriodicalIF":0.0,"publicationDate":"1995-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"19717742","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Cloning and expression of Kluyveromyces fragilis LAC4 gene.","authors":"K Huo, Y Li","doi":"","DOIUrl":"","url":null,"abstract":"<p><p>The genomic library of Kluyveromyces fragilis was constructed in E. coli TG1, and 5 beta-galactosidase gene (LAC4) clones have been obtained from the library by complementation of the Kluyveromyces lactis lac4-8 mutation. The studies on the structure and the function of the LAC4 gene revealed that (i) the gene can also complement E. coli lacZ mutation; (ii) the physical map of the K. fragilis LAC4 gene was very similar to that of K. lactis; (iii) the beta-galactosidase levels expressed by the clone strains were much higher than that expressed by the original strain; (iv) the variation of the beta-galactosidase level of different clone strains induced by lactose or galactose was related to the retained degree of the 5' flanking region of LAC4 gene, suggesting that there might be a lactose specific transcription activating element in the region.</p>","PeriodicalId":21648,"journal":{"name":"Science in China. Series B, Chemistry, life sciences & earth sciences","volume":"38 11","pages":"1332-40"},"PeriodicalIF":0.0,"publicationDate":"1995-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"19717743","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"H 2 +NO→H+HNO( 3 A ″)选态反应动力学理论研究","authors":"李顺来 李宗和 冯文林, Li Zong-He Feng Wen-Lin Li Shun-Lai","doi":"10.1360/ZB1995-25-10-1026","DOIUrl":"https://doi.org/10.1360/ZB1995-25-10-1026","url":null,"abstract":"对H 2 +NO→H+HNO反应,用从头算方法(UHF/6-31G)做了IRC解析,计算活化能与实验值相符。用Miller的反应Hamilton理论进行了反应动态学分析,指出H 2 及NO振动模式可近似地被认为是可分离的模。并用Truhlar等的选态反应速率理论计算了高振动激发态的选态反应速率常数,获得与实验相近的结果。","PeriodicalId":21648,"journal":{"name":"Science in China. Series B, Chemistry, life sciences & earth sciences","volume":"411 1","pages":"1026-1032"},"PeriodicalIF":0.0,"publicationDate":"1995-10-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"73584758","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Cloning, expression and characterization of a single-chain antibody PS-9 targeted to pancreatic cancer.","authors":"X Yan, B Tien, L Li, M Yuan","doi":"","DOIUrl":"","url":null,"abstract":"<p><p>Genes encoding single-chain antibodies have been first constructed, which consist of the heavy and light chain variable domains of antibody PS-9 joined together by a flexible peptide linker. The genes were cloned into coat protein g3p genes of pCANTAB5 phagemids, and expressed as fusion proteins on the phage tips. Immunological assay demonstrated that the engineered antibodies specifically bound to cancer cells LS-174-T as well as to pure bovine submaxillary gland mucin. Their specificity and affinity appeared the same as their parent antibodies. Our results supposed that the single-chain antibodies will be a target for the diagnosis and treatment of cancer.</p>","PeriodicalId":21648,"journal":{"name":"Science in China. Series B, Chemistry, life sciences & earth sciences","volume":"38 10","pages":"1230-6"},"PeriodicalIF":0.0,"publicationDate":"1995-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"19535542","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}