重组逆转录病毒载体的包装

将3.7kb的LacZ基因片段克隆到含标志基因Neo的逆转录病毒载体，pLXSN与pLNCX的多克隆位点，构建了含有LacZ基因的重组逆转录病毒载体pLLSN和pLNCL.在测定了G418对饥装细胞系PA317的最小致剂量后（最小致死剂量为0.3g/L），通过脂质体Lipofectin与磷酸钙2种介质，分别将2种重组逆转录病毒载体导入包装细胞系PA317进行包装，并以0.3g/L，的G418进行筛选，得到多个G418抗性克隆，经扩大培养，传代，分别得到包装pLLSN与pLNCL的2株阳性细胞，电镜下可见阳性细胞的培养上清中具有逆转录病毒形态特征的成熟病毒粒子，本0研究为运用逆转录病毒载体系统，解决转角因效率低的问题奠定了基础。     

有源负载恒温槽性能分析

本文阐述了有源负载恒温槽的工作原理，推导了描述其静态特性的缩减因数表达式，并对这种恒温槽的性能和应用作出了评价。     

番茄果实采后一氧化氮处理对活性氧代谢的影响

 以番茄品种‘百利’为试材, 研究了NO处理对其采后活性氧代谢的影响。结果表明: NO处理可推迟果实呼吸和乙烯高峰的出现, 抑制O·₂ 和H₂O₂ 的累积, 保持了贮藏后期SOD、CAT、POD、APX 较高的活性以及GSH和AsA含量的较高水平, 延缓了MDA含量和膜相对透性的升高, 降低膜脂过氧化程度, 延缓了果实衰老。     

Functional Analysis of ABC Transporter Genes From Botrytis cinerea Identifies BcatrB as a Transporter of Eugenol

The role of multiple ATP-binding cassette (ABC) and major facilitator superfamily (MFS) transporter genes from the plant pathogenic fungus Botrytis cinerea in protection against natural fungitoxic compounds was studied by expression analysis and phenotyping of gene-replacement mutants. The expression of 11 ABC (BcatrA–BcatrK) and three MFS genes (Bcmfs1, Bcmfs2 and Bcmfs4) was studied. All genes showed a low basal level of expression, but were differentially induced by treatment with cycloheximide and the plant defence compounds camptothecin, eugenol, psoralen, resveratrol and rishitin. The latter compounds induced expression of BcatrB at a high level. Eugenol was more toxic to BcatrB gene-replacement mutants than to the control isolates. Eugenol also caused an instantaneous increase in mycelial accumulation of the fungicide fludioxonil, a known substrate of BcatrB. However, there was no difference in virulence between the wild-type and BcatrB gene-replacement mutants on Ocimum basilicum, a plant known to contain eugenol. The results indicate that BcatrB is a transporter of lipophilic compounds, such as eugenol, but its role in virulence remains uncertain.     

冰核细菌对仁用杏胚珠超微结构的影响

 应用透射电镜对两个仁用杏品种‘白玉扁’和‘一窝蜂’接种冰核细菌并低温处理后的胚珠超微结构进行了观察, 发现冰核细菌对胚珠的超微结构有一定影响: (1) 使珠心细胞发生严重的质壁分离,细胞质中存在大量泡状结构, 线粒体的内部结构完全被破坏, 呈透明状, 而且有些珠心细胞中形成同心圆状的多膜内含物; (2) 使胚囊中卵细胞的细胞核外膜膨胀, 甚至核膜局部解体, 细胞质中细胞器减少。这些变化致使胚珠发育不正常, 影响受精而导致减产或绝收。接种冰核细菌并低温处理比单纯低温处理对胚珠超微结构的破坏程度重。     

党参小包装饮片养护方法研究

[目的]通过对比不同包装、贮藏条件对党参小包装饮片内外质量的影响,建立适合党参小包装饮片的养护贮藏方法.[方法]党参饮片分别采用聚乙烯塑料、铝箔、牛皮凝膜纸袋3种包装材料包装,做真空/非真空处理后,藏于不同温湿度的环境中,定期考察外观性状、水分、浸出物、多糖及其总黄酮等指标的变化.[结果]前6个月内,各组的检测指标均无明显变化;12个月时,非真空包装样品中的多糖、总黄酮含量均呈显著变化,且室温下贮存的纸袋包装样品出现了虫蛀,色泽变暗、变深的现象;18个月时,除真空包装冷藏处理的各样品以及阴凉条件下的铝箔真空包装样品各检测指标与0个月差异不大外,其余均有明显的性状或含测指标变化.[结论]结合养护成本综合考虑,党参小包装饮片可采用真空塑料或铝箔包装,存放于阴凉干燥处.     

酸奶营养品质提升的加工工艺研究

牛奶中含有丰富的活性营养物质,包括乳铁蛋白、免疫球蛋白、乳过氧化物酶、α-乳白蛋白、β-乳球蛋白等。传统工艺生产的酸奶经过高温杀菌,活性营养物质几乎完全损失。为了避免这一情况,本文推出一种新的酸奶生产工艺,生产出的酸奶可保留大部分活性营养物质。首先将牛奶的乳脂进行分离,乳脂部分进行125 ℃、5 s杀菌,脱脂牛奶部分进行75 ℃、15 s杀菌,将两部分料液混合后加入菌种发酵至酸度75~85°T,破乳后冷却后熟8 h以上。经测定,新工艺酸奶中α-乳白蛋白、β-乳球蛋白、乳铁蛋白、免疫球蛋白、乳过氧化物酶含量分别为966 mg/L、1 963 mg/L、23.4 mg/L、102 mg/L、1 025 U/L,远高于传统工艺酸奶的68 mg/L、200 mg/L、0.7 mg/L、14 mg/L、0 U/L。通过对比新工艺与传统工艺酸奶保质期内的活菌数、黏度、酸度和口感,并无显著差异。     

环保包装及环保包装的设计

在当今社会,包装扮演着越来越重要的角色.本文从实际出发,阐述了环保包装的重要性,环保包装是未来包装行业的发展趋势.文章从包装材料、设计等方面进一步阐明了环保包装的设计理念、设计方法,并且明确了作为设计师的职责及作为社会公民应具有环保意识.环保的设计理念必将成为未来包装行业的核心理念,环保、绿色包装是时代发展的必然要求.     

果蔬籽油生物活性研究进展

果蔬籽油是由果蔬籽经压榨或萃取工艺制得的植物油脂。果蔬籽油含有丰富的维生素、多不饱和脂肪酸、有机酸等活性成分,这些成分赋予了果蔬籽油抗氧化、抗癌、调节血脂和调节免疫系统等生物活性。本文综述了果蔬籽油生物活性的研究进展,旨在为果蔬籽油的综合开发和利用提供理论依据和指导。     

Establishment and Optimization of INH Epitope Peptide Vaccine for Detection of Antibody

In this study, an indirect ELISA method was established to detect inhibin hormone (INH) epitope peptide vaccine antibody, it would provide oretical reference for the determination of Fine-wool sheep after active immune body INH epitope peptide vaccine antibody. On the basis of the predecessors, using indirect ELISA method to determinate serum INH epitope peptide antibody levels of sheep, and through control different experimental conditions to look for the best experimental conditions. Through explorating the experimental conditions, finally, the testing experiment conditions were determined, which was blocked solution with skimmed milk powder, INH and GnIH synthetic peptides dilution degrees for 20 000 times, the optimum reaction time was 60 min, the best color action time was 15 min. In this experiment, a kind of method to detection antibody in the body after INH active immune sheep was built, it would provide a reference for future research.