Molecular cloning of a Mycoplasma meleagridis-specific antigenic domain endowed with a serodiagnostic potential

A recombinant phage library harbouring Mycoplasma meleagridis (MM) genomic DNA fragments was generated in the bacteriophage lambda gt11 expression vector. The library was screened for expression of MM specific antigens with a polyclonal antiserum that had been preadsorbed with antigens of the most common unrelated avian mycoplasma species. A 49-amino acid antigenic domain unique to MM was isolated, expressed in Escherichia coli, and its serodiagnostic potential was demonstrated. An antiserum raised against this MM-specific antigenic domain recognized a cluster of seven membrane-associated MM proteins with molecular masses ranging from 34 to 75 kDa. Overall, this study resulted in the identification of a potent serodiagnostic tool and revealed the complex antigenic nature of MM.     

国内外致泻大肠埃希氏菌O157:H7的检测标准比较及建议

致泻大肠埃希氏菌O157:H7（STEC O157:H7）是大肠埃希氏菌中致病性最严重的一种食源性致病菌,主要存在于牛肉、牛奶、水果及其制品中,对身体健康造成很大危害,甚至引发死亡。食品中STEC O157:H7检测尤为重要。本文对国内外STEC O157:H7的检测标准进行比较,提出我国标准在样品前处理、快速筛选方法的应用等方面需要加强,以便为该菌快速准确检测提供帮助,实现与国际标准化体系建设接轨,满足实验室检测需要。     

白菜型油菜DFR基因的克隆与序列分析

By using RACE (rapid amplification ofcDNA ends) based homologous cloning strategy, we have successfully isolated the genomic and full-length cDNA sequences of a gene encoding typical DFR (dihydroflavonol-4-reductase) from black-seeded Brassica campestris L. var. oleifera DC.. The gene, designated BcDFR here, is 1 722bp in length and harbors 5 introns with typical splice sites of plant DFR genes. BcDFR cDNA is 1311bp in length with a 1 158bp ORF as well as a 25bp 5‘ UTR and a 128bp 3‘ UTR. The encoded BcDFR protein is 385 aa with a calculated Mw of 42.85kD and a pI value of 5.55. The nucleotide and amino acid sequences of this gene share extensive homologies to plant DFR genes of wide origins especially high similarities to Cruciferous DFR genes. Sequence analyses such as phylogenetic analysis, conserved domain search and substrate specificity region detection all indicated that BcDFR gene is a quite potentially biofunctional gene. Its cloning enables us to further dissect the possible relatedness between DFR gene and Brassica seed coat color traits and to create transgenic novel yellow-seeded rapeseed germplasm through antisense- or RNAi-suppression of DFR gene expression in black-seeded elite cultivars.     

基于ARM7的智能灌溉模糊控制系统

介绍了基于ARM7和模糊控制算法开发的温室花卉智能灌溉系统。软件设计中移植了 操作系统，采用多任务程序设计方法设计，大大降低了编写程序的复杂度。针对灌溉过程中营养液混合系统的时变性、延时性、随机性等特点，提出采用模糊逻辑控制技术来实现系统的控制。在一定程度上解决了传统控制方法不易得到系统数学模型，难于对控制系统进行有效控制的不足。实践表明系统设计可靠，能够达到良好的控制效果。     

分解蔗渣的研究I.菌株的选育及其固态发酵条件的研究

从蔗渣腐烂域筛选出一株高纤维素酶活力的特异青霉（Ｐ．ｎｏｔａｔｕｍ）ＹＢ－５，经紫外线和亚硝基胍诱变，获得一突变株ＹＢ－７，其生长快，产孢子多且无毒性。并研究了碳源、氮源、金属离子和表面活性剂对产酶的影响。在正交优化的固体培养基和优化培养条件下，６０ｈ时ＣＭＣａｓｅ、ＦＰＡ和β－葡萄糖苷酶活力分别可达２９．４ＩＵ／ｍｌ、８．４０ＩＵ／ｍｌ和２５．１ＩＵ／ｍｌ。     

高校数字图书馆有效服务模式研究

在分析高校数字图书馆有效服务模式、主要特征的基础上,构建了一个以用户为中心的高校数字图书馆这一信息服务模式,并探讨了实现这一有效服务模式的途径与策略。

     

网络环境下省疾控中心图书馆工作

网络环境下,疾控中心图书馆应围绕其职能特点提供服务,其建设目标是收集和提供信息资源、提高信息咨询能力、提供专题化信息服务和加强员工的培训,因此必须加强图书馆人才队伍建设。     

面向用户服务体系的图书馆形态

面向用户服务体系的流动图书馆、盲人图书馆、家庭虚拟图书馆、电视图书馆、手机图书馆和泛在图书馆的本质和使命就是为一切用户服务。     

高校图书馆批量退证系统的设计与实现

针对高校图书馆在毕业生退证高峰期所面临的问题,介绍了惠州学院图书馆批量退证系统的设计目标及思路,并对批量退证系统实现过程中对相关表的解读、数据库的连接方法和功能的实现过程进行了详细的论述。