荧光灯灯头的快速自动化装配方案设计

荧光灯灯头装配的最大特点在于要求速度快、成本低，本文以GB13－02型荧光灯灯光为例，对其装配过程进行了详细的研究。并对灯头的自动化装配单元中装配动作最多的装配工位提出了合理的设计方案，为实现灯头快速自动化装配打下了基础。     

3-苯基-7-氨基香豆素的合成及应用

3 ,7 取代香豆素类荧光增白剂的白度高、耐光性能优良、增白后的制品不带蓝光头或红光头 ,制品外观更悦目 ,具有更高的商业价值 ,广泛用在纺织印染业和塑料加工业。这类荧光增白剂生产工艺较复杂 ,国内对此研究不多 ,目前达到工业化规模生产的几乎还是空白 ,国内市场需要的品种都是从国外进口 ,具有潜在的市场前景。而 3 苯基 7 氨基香豆素是合成该类荧光增白剂的重要中间体 ,本文介绍了 4种合成该中间体的工艺路线     

6-甲氧基-2-[5-甲氧基-2-(4-甲基苯磺酰氨基)]苯基-4-苯并噁嗪酮的合成及荧光性能

以3 羟基苯甲醛为原料,通过硝化、醚化、氧化、还原等过程,找出制备中间体5 甲氧基邻氨基苯甲酸的较佳条件。在吡啶中,5 甲氧基邻氨基苯甲酸和对甲苯磺酰氯反应,得到荧光发射波长为590nm的荧光剂6 甲氧基 2 [5 甲氧基 2 (4 甲苯磺酰氨基)]苯基 4 苯并口恶嗪酮,并配制油墨:黏度54 3Pa·s,黏性4 71,细度11μm。适应于轮转胶印印刷。     

生物标记用发光材料研究现状

综述了生物标记用材料及其应用,对各种材料的特点进行了分析,得出以绿色荧光蛋白等为代表的荧光材料将是未来生物标记的主流.     

日光照射对荧光增白剂VBL顺-反异构现象影响的研究

用紫外光谱和荧光光谱法对日光照射荧光增白剂VBL溶液进行了研究。结果表明、随日光照射时间的延长，VBL溶液在432nm处荧光强度下降；而在267nm处有所增强，低浓度溶液对日光照射更加敏感。1mg／1在避光时测得吸光度为0.449，而在日光照射15分钟后，其吸光度下降至0.141，证明日光照射使VBL溶液中的顺式异构体增加。     

Lanthanide-binding tags as versatile protein coexpression probes

Comprehensive proteomic analyses require new methodologies to accelerate the correlation of gene sequence with protein function. Key tools for such efforts include biophysical probes that integrate into the covalent architecture of proteins. Lanthanide-binding tags (LBTs) are expressible, multitasking fusion partners that are optimized to bind lanthanide ions and have several desirable attributes, which include long-lived luminescence, excellent X-ray scattering power for phase determination, and magnetic properties to facilitate NMR spectroscopic structure elucidation. Herein, we present peptide sequences with a 40-fold higher affinity for Tb(3+) ions and significantly brighter luminescence intensity compared with existing peptides. Incorporation of an LBT onto ubiquitin as a prototype fusion protein allows the use of powerful protein-visualization techniques, which include rapid luminescence detection of LBT-tagged proteins in SDS-PAGE gels, as well as determination of protein concentrations in complex mixtures. The LBT strategy is a new alternative for expressing fluorescent fusion proteins by routine molecular biological techniques.     

荧光染料用于涤纶织物染色的荧光性能研究

在实验条件下，染色织物的荧光反射率随荧光染料的浓度增加而增加，超过一定浓度后，有下降趋势；在pH=5左右，荧光反射率最高；荧光增白剂会提高染色织物的荧光反射率，在荧光黄2GFL中，当荧光增白剂的浓度由0.1％增加到5％时，荧光反射率由8．43增加至18．59，而对非荧光染料只有增艳的作用，不产生荧光。荧光染料染色织物的荧光反射率随着加入非荧光染料量的增加而减弱。     

煤的荧光特性与其工艺性能的关系研究

简述了煤中镜质组荧光产生的机理及荧光参数的测量方法,通过测定一系列煤的粘结性和10kg小焦炉结焦性试验,探讨了煤的荧光特性与其工艺性能的关系。煤的荧光参数与其反射率呈正的线性相关关系,与其挥发分含量呈负的线性相关关系;煤的粘结性、结焦性均与其荧光参数有关;当煤化程度相同、煤岩组成基本相同时,煤的荧光强度愈强,其结焦性能愈好。     

新型不对称结构荧光增白剂的合成及其性能

用4-硝基-4′-氨基二苯乙烯-2,2′-二磺酸替代4,4′-二氨基二苯乙烯-2,2′-二磺酸,与三聚氯氰和氨基化合物经过四步缩合得到2个新型不对称结构和用作参比的3个传统对称结构荧光分子。对比研究这两类增白剂在水溶液中的紫外吸收、荧光发射、光致异构化现象及其应用性能。结果显示不对称结构增白剂紫外吸收和染色性能提高,但其荧光发射性能下降,且同样存在较为明显的光致异构化现象,耐光性也较差。     

Construction, properties and specific fluorescent labeling of a bovine prothrombin mutant engineered with a free C-terminal cysteine

To define the role of phosphatidylserine-induced conformationalchanges in prothrombin activation during blood coagulation,a recombinant bovine prothrombin was constructed, characterizedand shown to have a globally native-like conformation. We introduceda cysteine to replace the penultimate residue (Gly581) of apreviously constructed active site mutant, and expressed thedouble mutant in Chinese hamster ovary cells at the level of0.6 µg/ml of cell culture medium. Specific labeling withfluorescein maleimide was accomplished by limited reductionwith dithiothreitol to free the engineered cysteine while maintainingthe native-like functional properties of the molecule. The averagestoichiometry of labeling was 0.84 probe/protein. The locationof the probe at the C-terminus was confirmed by proteolysisby native thrombin, by Taipan venom, and by carboxypeptidaseY. Both the double mutant and labeled prothrombin could be activatedby snake venoms and the prothrombinase but, as expected, thedouble mutant meizothrombin did not autolyze as does nativemeizothrombin. Thus, for the first time, a native-like but specificallylabeled prothrombin has been constructed. This molecule willbe an essential tool for elucidating the structural role ofmembranes during prothrombin activation. In addition, the methodsdescribed might be usefully applied to labeling of an odd, engineeredcysteine in other disulfide bond-containing proteins.