服务质量管理体系在大学图书馆中的应用

本文介绍了服务质量管理体体系及其在大学图书馆中的应用,以实例说明图书馆服务质量管理的内容,以及服务质量管理测评对图书馆产生的效益。     

副猪嗜血杆菌单克隆抗体的制备及其B细胞抗原表位的鉴定

为筛选具有临床诊断价值的副猪嗜血杆菌(H.parasuis)单克隆抗体(MAb),本研究采用H.parasuis 5型强毒株(HPS-5)免疫BALB/c小鼠,利用常规细胞融合技术制备了一株稳定分泌MAb的杂交瘤细胞株。Western blot结果表明该MAb能够特异性识别所有H.parasuis标准菌株;免疫共沉淀技术与蛋白质谱分析显示该MAb所识别的蛋白为ATP结合盒转运蛋白(ABCT)家族的寡肽透过酶(OppA);利用MAb对噬菌体12肽库进行淘选,8个阳性噬菌体克隆展示有"KTPAE-R"保守序列,对应于H.parasuis SH29755株和SH0165株的469位~475位的氨基酸残基。对OppA氨基酸序列比对结果表明H.parasuis与其它10种猪常见细菌病病原序列一致性为9.1%~74.5%,本研究结果为进一步研究H.parasuis感染的病原学诊断建立了良好的基础。     

我国绿系蜂胶的探讨

绿系蜂胶的概念主要来自巴西蜂胶。近些年来，我国出现的大炒巴西蜂胶的现象源于对巴西蜂胶狭隘和浅薄的认识及商业利益的驱动。我们通过赴巴西对巴西蜂胶及相关情况的实地考察，引发了我们对以巴西蜂胶为代表的绿系蜂胶的探讨。     

木耳菌糠袋栽滑菇配方研究

本试验采用不同比例的木耳菌糠替代部分木屑袋栽滑菇,以培养料（木屑89%、麦麸10%、石膏1%）为对照,探讨木耳菌糠栽培滑菇的可行性。结果表明,木耳菌糠添加量25%～45%时,可缩短发菌天数,其中菌糠添加量为45%时,满袋天数仅需52 d,并且长势较好;但菌糠添加量为55%～65%时,则延长了发菌天数,而且菌丝稀疏,长势也弱。对照（CK）与木耳菌糠添加量是25%～45%时,子实体生长良好,并且出菇整齐;菌糠添加量为55%～65%,则出菇不整齐。CK的生物学效率最高,但配方4（菌糠45%、木屑34%、麦麸10%、石膏1%）的生物学效率与CK差异不大,从成本和生态效益考虑,配方4栽培滑菇具有可行性,并已在广灵县进行推广。     

硅酸盐解钾菌对含钾矿物的选择性风化机理

从棉花根际土壤中筛选、分离、纯化了硅酸盐解钾菌,进行了硅酸盐解钾菌与7种含钾矿物在厌氧密闭系统中的生物风化解钾试验,探讨了硅酸盐解钾菌对不同含钾矿物生物风化作用的规律。试验结果表明,生物风化反应释放出K+最多的前3个组合是白云母和QY17、黑云母和QY19、白云母和QY19,反应释放出K+的量分别为1 235.76、1 010.71、916.61μg/g。生物风化反应固定K+最多的4个组合是黑云母和QY4、蒙脱石和QY3、黑云母和QY10、高岭石和QY17,反应中含K矿石固定K+的量分别为78.35、39.92、32.71、22.56μg/g。形成差异的原因可能是硅酸盐解钾菌(包括其次生代谢物)与含钾矿物的晶体结构之间的双向选择过程。硅酸盐解钾菌浓度越大,硅酸盐解钾菌类群对矿物生物风化作用有选择性倾向越明显。造成硅酸盐解钾菌的解钾数量、速率的差异的原因是界面交换过程的不同,机理是硅酸盐解钾菌(次生代谢物)与含钾矿物之间空间构效关系(CQSAR)。风化作用是硅酸盐细菌剥蚀作用、机械破碎、次生有机酸解钾过程交替循环所产生的。腐殖酸的加入促进了硅酸盐解钾菌解钾的过程,延长了解钾时间,同时向硅酸盐解钾菌提供C、N养分。     

Evaluation on Tolerance of Montmorillonite as a Mycotoxin Adsorbent

In order to study the tolerance dose of Kunming mice to montmorillonite as a mycotoxin adsorbent in diets,the experiment selected 60 healthy male Kunming mice with initial average body weight of (17±0.12)g,randomly divided them into 5 treatments with two replicates per group and 6 mice per replicate.Five experimental diets were added to 0 (control group),0.5%,1%,2% and 5% montmorillonite,respectively.After 30 days,the growth performance,nutrients apparent digestibility,serum biochemical indices and internal organization were tested to determine the tolerance dose of montmorillonite for Kunming mice.The results showed that the ADFI was significantly increased in 0.5% group (P< 0.05),while there were no significant differences in ADFI and ADG between 1% group and control group (P> 0.05),then the ADFI was significantly decreased with the increasing of montmorillonite supplemental level (P< 0.05).The ADG in 2% group had no significant difference when compared with the control group (P> 0.05),while significantly lower than that in 0.5% and 1% groups (P< 0.05).The apparent digestibility of DM,CP and EE showed no significant effect at any level of montmorillonite (P> 0.05).Serum ALT,AST activities and MDA content were gradually increased with the montmorillonite supplemental level increasing,and that in 1%,2% and 5% groups were significantly higher than that in control group (P< 0.05),but there were no significant differences between 0.5% group and control group (P> 0.05).Tissue sections showed that mice livers were damaged in varying degrees when the montmorillonite supplemental level was 5%.In conclusion,based on a comprehensive consideration of all indexes,it could be seen that the tolerance dose of the tested montmorillonite for Kunming mice was between 0.5% and 2% when mycotoxin contents in diets were in security range.     

教室排椅设计

大学校园是神圣、严肃的学术殿堂,教室里的排椅是学生求知、问道的物质基础.在大学校园中,排椅不仅仅为学生提供了听课、自习的基本使用功能,也通过其造型美感体现出学校的校园文化和学术气息[1].对于生产商来说,排椅是具有较高定制性和批量性特征的产品.一方面,生产商需要为学校设计适合其文化和理念的造型.另一方面,学校为了形成统一的校园文化和形象,对排椅产品的需求量比较大,要求生产商能够提供大批量的产品.因此,排椅设计的研究有非常重要的现实意义.笔者将重点从大学教室排椅的功能和造型两个方面进行论述.     

F-box domain is involved in regulating the proliferation of MCF-7 cells by FBXO39 protein

AIM: To investigate the effect of F-box domain on the regulation of MCF-7 cell proliferation by FBXO39 protein. METHODS: The effect of F-box domain on the localization of FBXO39 protein in the MCF-7 cells was investigated. MCF-7 cell cDNA library was used as the template resource. The full-length cDNA sequence of FBXO39 was amplified by PCR method and subcloned into eukaryotic expression vector pEGFP-C2. The pEGFP-FBXO39ΔF (F-box domain deletion mutation) plasmid was successfully constructed with the template resource of pEGFP-FBXO39 plasmid. The recombinant plasmids were transfected into the MCF-7 cells, and then the expression of FBXO39 and FBXO39ΔF were determined by Western blot. The cellular localization of FBXO39 and FBXO39ΔF were observed by confocal microscopy. The localization of endogenous FBXO39 in the MCF-7 cells was detected by immunofluorescence staining. In addition, MTT and EdU assays were used to measure the cell proliferation, flow cytometry was used to measure the cell cycle distribution, and immunohistochemical staining was used to observe the expression of FBXO39 in the breast cancer and para-carcinoma tissues. RESULTS: The eukaryotic expression vector pEGFP-FBXO39 and pEGFP-FBXO39ΔF were constructed successfully. F-box domain had no effect on the cell localization of FBXO39. FBXO39 promoted MCF-7 cell proliferation but FBXO39ΔF did not. FBXO39 was highly expressed in the breast cancer tissues. CONCLUSION: F-box domain had no effect on the cellular localization of FBXO39 protein. However, it plays an important role in the biological function of FBXO39. FBXO39 may be related to breast cancer tumorigenesis.