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酶工程在医药工业中的应用 总被引:1,自引:0,他引:1
酶工程是现代生物技术的重要组成部分,它作为一项高新技术将为各工业的发展起重要推动作用。介绍了酶固定化、基因工程菌(细胞)的固定化、植物细胞培养产酶、酶的化学修饰、核酸酶、抗体酶、酶标药物的理论和技术研究的最新进展以及酶工程在医药工业中的应用,对酶工程的发展前景进行了探讨。 相似文献
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二氯苯生产技术进展与发展趋势 总被引:7,自引:0,他引:7
介绍了二氯苯生产方法,用途,市场需求及发展趋势,重点介绍了二氯苯异构体分离技术,针对国内对,邻二氯苯生产现状,提出一些发展建议。 相似文献
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论述了深入研究中药制剂分离技术创新进展的意义,概述了固液分离技术在中药制剂中的重要作用,首次全面总结了14种制药分离与纯化主要设备的重大发展历程及创新特征,首次系统剖析了14种中药制剂提取分离与纯化高新技术原理特性和应用效果,首次研究阐明了现代中药制剂分离与纯化技术主要呈现的新老技术复合化、高技术超常化和新技术多样化三大发展趋势。 相似文献
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阐述了酶应用的历史起源及酶在化工中应用的发展过程,介绍了酶在化学工业中的覆盖面、地位和现状以及生物工程酶与化工融合发展的潜力和趋势. 相似文献
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我国在80年代初即将生物工程确定为科技和产业发展的重要领域,制订了发展的战略目标和具体规划,组织了攻关队伍,采取各种措施,使我国生物工程的发展走上了有计划的迅速发展道路,取得了许多重大的突破性进展,为在本世纪末形成一定规模的生物工程新产业,跻身世界生物工程先进行列,打下了坚实基础。 相似文献
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目录导言1什么是假体生物工程材料?2假体生物工程材料制备方法2.1金属粉末焙烧2.2造孔剂的应用2.3电场活性固化2.4复制方法 相似文献
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用酶防污,消除毒素对环境的危害,这是环境友好型防污涂料的重要发展方向之一。阐述了酶防污涂料的发展历程、防污机理以及就"留住"防污涂料中的酶及其发展前景作了粗浅的探索。 相似文献
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P. D. Sarkisov E. G. Vinokurov N. B. Gradova E. S. Babusenko V. V. Bondar’ 《Theoretical Foundations of Chemical Engineering》2013,47(1):14-18
The possibility of implementing a new scientific field—bioengineering of glass surface—was considered. The growth of different diatom algal cultures and the density of their immobilization on the surface of glass were studied. The experimental results that confirm the possibility of the bioengineering formation of glass surface micro- and nanostructures using diatom algae were represented. 相似文献
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Arie J. Zuckerman 《Journal of chemical technology and biotechnology (Oxford, Oxfordshire : 1986)》1988,43(4):301-311
It has been said that ‘never in the history of human progress has a better and cheaper method of preventing illness been developed than immunisation’. This is well illustrated by the WHO Expanded Programme on Immunisation (EPI), which in developing countries is now preventing nearly a million deaths annually from measles, pertussis, and neonatal tetanus, and for which there is a commitment by the WHO and UNICEF to protect all children by immunisation by the end of the decade. This enormous undertaking will be facilitated by the rapid advances in molecular biology and recombinant DNA technology, in the understanding of immunological mechanisms and by the production and application of monoclonal antibodies so that the structure and location of important antigenic determinants or epitopes can be determined. Chemical synthesis of oligopeptides has been simplified, and computer programmes and X-ray crystallography provide the tools for the determination of three-dimensional structure of proteins, so that the structure and location of important antigenic determinants or epitopes can be predicted. These techniques have opened the way to the improvement of existing vaccines and to the development and production of new vaccines against infections for which vaccines are not available. New vaccines under development include vaccines against hepatitis B, hepatitis A, malaria, vaccines for typhoid, cholera, rotavirus infection and other diarrhoeal diseases, leprosy, rabies, fertility regulating vaccines and the acquired immune deficiency syndrome (AIDS). 相似文献
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Giulio Gasparini Marta Dal Molin Stefano Corrà Patrizia Galzerano Paolo Scrimin Leonard J. Prins 《Israel journal of chemistry》2013,53(1-2):122-126
The development of a serine protease model using a self-selection protocol is described. The developed system mimics the regeneration step of an enzyme involved in covalent enzyme catalysis. A transition-state analogue of a transesterification reaction is used to self-select functional groups able to accelerate ester cleavage. It is shown that the insertion of a tertiary amine substituent flanking the reaction center reinforces transition-state stabilization by directing the reactive center towards the self-selected functionality. In addition, the tertiary amine activates a bland (solvent) nucleophile for attack on an ester bond similar to what occurs in a serine protease. A quantitative correspondence is observed between the amplification factors and catalytic activity, illustrating the potential of the dynamic covalent capture strategy to precisely detect and quantify weak noncovalent interactions. 相似文献
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Inflammatory processes occur as a generic response of the immune system and can be triggered by various factors, such as infection with pathogenic microorganisms or damaged tissue. Due to the complexity of the inflammation process and its role in common diseases like asthma, cancer, skin disorders or Alzheimer's disease, anti-inflammatory drugs are of high pharmaceutical interest. Nature is a rich source for compounds with anti-inflammatory properties. Several studies have focused on the structural optimization of natural products to improve their pharmacological properties. As derivatization through total synthesis is often laborious with low yields and limited stereoselectivity, the use of biosynthetic, enzyme-driven reactions is an attractive alternative for synthesizing and modifying complex bioactive molecules. In this minireview, we present an outline of the biotechnological methods used to derivatize anti-inflammatory natural products, including precursor-directed biosynthesis, mutasynthesis, combinatorial biosynthesis, as well as whole-cell and in vitro biotransformation. 相似文献