The Study On Chinese Copyright Pledge system

质押是著作权利用制度的重要组成部分，但我国现行法律规范对其实体内容规定不多。随着人们对知识产权重要性的认识增强，著作权质押将会更多的用于实践中。本文主要从以下三章来分析著作权质权。 第一章介绍了著作权质押的概念和法律依据。著作权是民法上的私权利，著作权质押是一种权利质押，通过一般性的分析，界定好著作权质押的概念，为著作权的质押找到了《物权法》、《担保法》、《著作权法》等方面的法律依据。此外，第二节对著作权质押的性质特征进行分析，著作财产权具有可质性，著作权包括著作人格权和著作财产权，明确了著作权质押的是著作财产权；此外，著作权是一种无形的财产权，因此，著作权质权除了具备一般权利质权的性质外...The copyright pledge is an important part of the copyright-use system.However,there is not much regulation content in the current law regulation. With the enhancement in the recognition of the importance of intellectual property rights,the copyright will be more applied in practice.The article which includes three parts will analyze the copyright pledge: The first part describes the concept and ...学位：法律硕士院系专业：法学院法律系_法律硕士(JM)学号：1302009115029

光环境生物效应及其模拟实验装备研究进展

光是人、动物和植物赖以生存的基本条件。光环境作为一种物理环境因素,其生物效应具有十分重要的理论和应用价值。光环境对人的生理、心理及行为产生重要影响,对动物昼夜节律、定位系统和生长繁育的影响也已受到诸多关注;同时,光是植物赖以生存的基础,是植物一切生化反应的能量来源。综述了光环境生物效应的研究进展,指出已有的文献仅限于以复色光为研究对象,对特定波长的光效应、光暴露时间及光质效应的研究甚少。进一步阐明目前光环境模拟实验装备的研制所遇到的关键\"瓶颈\"是缺乏能够在一定波长范围内输出较高功率的单色光光源,且无配备生物学培养装置,不可能在实验室实现对单色光环境的模拟。因此,其发展当务之急是先构建光环境暴露的科学实验平台。同时对光环境生物效应的研究方向及光模拟实验装备的应用前景进行了展望。中国科学院科研装备研制项目(YZ201104,YZ201303);中国科学院STS计划(Y6I0921A20)资

Research Progress of α-Glucuronidase, an Enzyme for Degrading Hemicellulose Side-Chain

半纤维素是自然界中最丰富的可再生资源之一,将半纤维素降解为单糖并转化为燃料或化学品一直是科学界研究的热点。半纤维素是由木糖基主链以及α-葡萄糖醛酸等侧链共同组成的异质多聚体。α-葡萄糖醛酸酶是半纤维素完全降解过程中的关键酶之一,能够水解4-O-甲基葡萄糖醛酸与木糖之间的α-1,2-糖苷键。本文综述了α-葡萄糖醛酸酶的分类、催化机制及晶体结构、酶学性质和基因克隆表达等方面的研究进展,同时对该研究进行了展望。Hemicellulose is one of the most abundant renewable resources in nature.The bioconversion of hemicellulose into biofuels or chemicals is a research hotspot in the world.Hemicellulose consists of a backbone of xylan residues and some branches like glucuronic acid.α-Glucuronidase, which is capable to hydrolysis the α-1,2-glycosidic bond between xylan and glucuronic acid, is one of the key enzyme to degrade hemicellulose completely.The recent research progresses on catalysis mechanism, structure, charaterization, and gene cloning of α-glucuronidase are summarized in this paper.国家自然科学基金(31170067;21303142); 国家重点基础研究发展计划(973计划;2010CB732201); 福建省自然科学基金(2012J05029); 农业部“引进国际先进农业科学技术”项目(2013-Z70

Cloning and heterologous expression of a novel GH10 xylanase gene from Hypocrea orientalis EU7-22

木聚糖酶是降解半纤维素最主要的酶,对于开发可再生生物能源具有重要的应用价值。分别以东方肉座菌(HyPOCrEA OrIEnTAlIS)Eu7-22的基因组dnA和C dnA为模板,利用染色体步移和PCr技术首次克隆获得该菌gH10家族木聚糖酶Ⅲ的基因(XynⅢ),并对其进行生物信息学分析。结果表明:该基因全长1283 bP(gXynⅢ),含有3个内含子;CdS序列为1044 bP(CXynⅢ),编码347个氨基酸,n端含有一个16 AA的信号肽序列;XynⅢ氨基酸序列与TrICHOdErMA PSEudOkOnIngII的EndOXylAnASE具有较高的同源性。经生物信息学分析,XynⅢ成熟蛋白可能含有18个n-糖基化位点,其理论等电点(P I)为6.14,蛋白质分子质量为36.55 ku,属于亲水性蛋白;SWISS-MOdEl建模预测,XynⅢ成熟蛋白中含有11个α螺旋,其核心结构为8个β折叠片围成一个柱状结构。同时将编码成熟蛋白的基因片段MXynⅢ与P PIC9k质粒连接构建表达载体后转化毕赤酵母,对重组子表达产物进行酶活检测显示该基因能在毕赤酵母中表达有生物活性的XynⅢ并分泌到胞外,发酵液中的木聚糖酶活在诱导培养168 H后可达到127.5 Iu/M l。Endo-1,4-xylanase( E.C.3.2.1.8) is the major enzyme to the conversion of hemicelluloses into xylo-oligosaccharide.In this research,a novel GH10 xylanase Ⅲ( xyn Ⅲ) gene was cloned from Hypocrea orientalis EU7-22 by chromosome walking and PCR.The results showed that the DNA fragment( 1283 bp) encoding xynⅢ( gxynⅢ) contained three introns.The CDS of xynⅢ( cxynⅢ) encoded 331 amino acids of putative mature protein and a 16 aa signal in N terminator.The amino acid sequence of xynⅢ is highly homologous with the endoxylanase of Trichoderma pseudokoningii.The bioinformatics analysis showed that the theoretical isoelectric point and the molecular weight of putative mature protein of XYNⅢ were 6.14 and 36.55 ku,respectively.It is a soluble hydrophilic protein containing 18 N-glycosylation sites.The 3D structure predicted with SWISS-Model showed that XYNⅢ protein contained11 alpha helices and 8 extended strands.A recombinant plasmid p PIC9K-xynⅢ was constructed and then transformed into Pichia pastoris.The transformant identified by PCR was induced to produce XYNⅢ enzyme with 1% methanol.And after 168 hours induced expression,the produced crude enzyme was detected to reach a high enzymatic activity of 127.5 IU / m L.国家自然科学基金(21303142;31170067); 福建省海洋高新产业发展专项项目(闽海洋高新[2014]25号); 厦门市海洋经济发展专项资金项目(14GZP59HJ29

Measurement of integrated luminosity of data collected at 3.773 GeV by BESIII from 2021 to 2024

We present a measurement of the integrated luminosity e+e- of collision data collected by the BESIII detector at the BEPCII collider at a center-of-mass energy of Ecm = 3.773 GeV. The integrated luminosities of the datasets taken from December 2021 to June 2022, from November 2022 to June 2023, and from October 2023 to February 2024 were determined to be 4.995±0.019 fb-1, 8.157±0.031 fb-1, and 4.191±0.016 fb-1, respectively, by analyzing large angle Bhabha scattering events. The uncertainties are dominated by systematic effects, and the statistical uncertainties are negligible. Our results provide essential input for future analyses and precision measurements

Determination of the number of ψ(3686) events taken at BESIII

The number of ψ(3686) events collected by the BESIII detector during the 2021 run period is determined to be (2259.3±11.1)×106 by counting inclusive ψ(3686) hadronic events. The uncertainty is systematic and the statistical uncertainty is negligible. Meanwhile, the numbers of ψ(3686) events collected during the 2009 and 2012 run periods are updated to be (107.7±0.6)×106 and (345.4±2.6)×106, respectively. Both numbers are consistent with the previous measurements within one standard deviation. The total number of ψ(3686) events in the three data samples is (2712.4±14.3)×10^