抗震高可靠电子枪的设计

电视跟踪、电视制导是导弹武器系统的重要组成部份,摄象器件又是其中的关键器件。本文着重从抗震、高可靠方面介绍摄象器件电子枪的结构和性能设计,该电子枪应用于重点军事工程,经多次试验和实际使用,性能稳定,达到了高可靠的要求,是目前国内唯一的抗震高可靠电子枪。     

自动送粉激光熔覆装置及工艺研究

研制了一种工作稳定性好、粉末流量连续可调的自动送粉装置。经A_3钢表面激光熔覆WF-150不锈钢合金粉末的研究表明,所获得的激光熔覆层均匀连续、无宏观气孔和裂纹,粉末利用率高达94％。     

纳米酶在食品保鲜中的应用

具有优异广谱抗菌特性的纳米酶,为解决由微生物引起的食品腐败问题提供了一种全新策略。纳米酶可在生理环境中催化相应的底物而产生活性氧,因其制备简便、成本低、催化效率高,易于规模化生产和稳定性高等优点,故在食品保鲜领域具有广阔的应用前景。本文综述纳米酶的分类,包括金属或金属氧化物基纳米酶、碳基纳米酶、聚合物基纳米酶及其它材料,调控纳米酶抗菌活性的主要因素(大小、形态、涂层及改性、组成成分等),为如何设计高效抗菌纳米酶提供了参考。本文还阐述纳米酶在食品保鲜中的应用,包括纳米酶基抗菌薄膜应用及其在检测食品中细菌污染水平中的应用。由于其广谱抗菌特性和可忽略的生物毒性,抗菌纳米酶能降低食品工业中微生物的危害,而且有助于控制食品生产及加工中的交叉污染问题,对保障食品安全,促进食品工业健康可持续发展具有十分重要的现实意义。总而言之,抗菌纳米酶有望成为一种新型的抗菌剂和/或策略,在食品保鲜中展现出广阔的应用前景。     

极大节旋藻(Arthrospira maxima)生物钟基因kaiC的克隆及分析

以kaiC基因簇部分已知序列为引物设计位点,采用PCR反应池法从节旋藻基因组fosmid文库中筛选到kaiC基因克隆,通过步移测序获得了kaiC基因全长序列。kaiC基因编码区长1554bo,基因GC碱基含量平均为41．76％,密码子第三位明显偏向于U。在基因上游385bp范围内发现一个可能的启动子序列和一些基因调控元件。KaiC蛋白分析发现了Walker A、DXXG、不完整的Walker B等重要模体和具有催化作用的功能位点。Southem杂交的结果证明kaiC基因在极大节旋藻中为单拷贝。极大节旋藻kaiC基因的特殊结构特征为研究kai基因簇的进化提供了重要的启示。     

测试条件对聚氯乙烯树脂稀溶液粘数的影响

聚氯乙烯树脂稀溶液粘数是聚氯乙烯树脂的一项重要指标,它的高低决定着产品的不同用途。本实验测试了几种不同测试条件如测试温度、黏度计毛细管直径、溶剂浓度等对聚氯乙烯树脂稀溶液粘数结果所产生的影响,通过实验数据的理论分析和计算,对原因进行了具体的分析。这些分析结果的获得对提高粘数分析的准确性,对于指导实际生产,规范检验操作,修订检验标准都有着重要的意义。     

混凝沉淀工艺对不同优势藻类的去除特性研究

为了考察混凝沉淀工艺的除藻性能在不同藻类优势期内的变化,将试验过程分为绿藻优势期和蓝藻优势期两个阶段,进行进水藻类群落结构特征及其变化对混凝沉淀除藻效能的影响研究.结果表明,混凝沉淀在绿藻优势期和蓝藻优势期的除藻效率分别为68.3%和40.4%,且各种藻类的去除效能并无明显的相互影响.蓝藻优势期的藻类去除率大大低于绿藻优势期,其根本原因在于占优势地位的微囊藻的生理生态特征.因此,把水中的所有藻类笼统地作为一个去除对象是不适宜的,应分析水中藻类群落结构特征,并根据特定原水中的优势藻种类进行针对性的除藻方案研究.     

Discovery of Five New Ethylene-Forming Enzymes for Clean Production of Ethylene in E. coli

Ethylene is an essential platform chemical with a conjugated double bond, which can produce many secondary chemical products through copolymerisation. At present, ethylene production is mainly from petroleum fractionation and cracking, which are unsustainable in the long term, and harmful to our environment. Therefore, a hot research field is seeking a cleaner method for ethylene production. Based on the model ethylene-forming enzyme (Efe) {"type":"entrez-protein","attrs":{"text":"AAD16440.1","term_id":"4323597","term_text":"AAD16440.1"}}AAD16440.1 (6vp4.1.A) from Pseudomonas syringae pv. phaseolicol, we evaluated five putative Efe protein sequences using the data derived from phylogenetic analyses and the conservation of their catalytic structures. Then, pBAD expression frameworks were constructed, and relevant enzymes were expressed in E. coli BL21. Finally, enzymatic activity in vitro and in vivo was detected to demonstrate their catalytic activity. Our results show that the activity in vitro measured by the conversion of α-ketoglutarate was from 0.21–0.72 μmol ethylene/mg/min, which varied across the temperatures. In cells, the activity of the new Efes was 12.28–147.43 μmol/gDCW/h (DCW, dry cellular weight). Both results prove that all the five putative Efes could produce ethylene.     

Exploring the Effects of the Interaction of Carbon and MoS2 Catalyst on CO2 Hydrogenation to Methanol

Hydrogenation of CO₂ to form methanol utilizing green hydrogen is a promising route to realizing carbon neutrality. However, the development of catalyst with high activity and selectivity to methanol from the CO₂ hydrogenation is still a challenge due to the chemical inertness of CO₂ and its characteristics of multi-path conversion. Herein, a series of highly active carbon-confining molybdenum sulfide (MoS₂@C) catalysts were prepared by the in-situ pyrolysis method. In comparison with the bulk MoS₂ and MoS₂/C, the stronger interaction between MoS₂ and the carbon layer was clearly generated. Under the optimized reaction conditions, MoS₂@C showed better catalytic performance and long-term stability. The MoS₂@C catalyst could sustain around 32.4% conversion of CO₂ with 94.8% selectivity of MeOH for at least 150 h.     

华蟾素注射液对人肝癌HepG-2细胞增殖及周期的影响

Objective: The aim of our study was to investigate the effect of Cinobufacini injection on the proliferation and cell cycle of human hepatoma HepG-2 cells. Methods: Cell proliferation was assessed by MTT assay, cell cycle distributionwas detected by the flow cytometry (FCM). The expression of Cyclin A, CDK2 mRNA levels were examined by RT-PCR.Quantitative colorimetric assay was used to analyze Cyclin NCDK2 activity in HepG-2 cells. Results: Cinobufacini injection significantly inhibited HepG-2 cells proliferation in dose- and time-dependent ways; FCM analysis showed Cinobufacini injection induced cell cycle arrest at S phase; RT-PCR assay showed Cinobufacini injection down-regulated Cyclin A, CDK2expression at mRNA levels; Quantitative colorimetric assay showed Cinobufacini injection deceased Cyclin A/CDK2 activity in HepG-2 cells. Conclusion: Cinobufacini injection can inhibit human hepatoma HepG-2 cells growth, induce cell apoptosis and induce cell cycle arrest at S phase, the mechanism of which might be partly related to the down-regulation of Cyclin A,CDK2 mRNA expression and inhibition of Cyclin A/CDK2 activity.