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应用16S rDNA序列同源性分析鉴定放射线照射后的口腔链球菌 被引量:2
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作者 佟卉春 东秀珠 高学军 《现代口腔医学杂志》 CAS CSCD 2004年第2期101-103,共3页
目的 对受放射线影响 ,糖发酵特征发生改变的口腔链球菌进行鉴定。方法 生理、生化试验 ;16SrDNA序列同源性分析 :提取待鉴定细菌的基因组DNA ,用多聚酶链式反应 (PCR)扩增 16SrDNA ,对其测序后输入GenBank中与已知序列进行比较。结... 目的 对受放射线影响 ,糖发酵特征发生改变的口腔链球菌进行鉴定。方法 生理、生化试验 ;16SrDNA序列同源性分析 :提取待鉴定细菌的基因组DNA ,用多聚酶链式反应 (PCR)扩增 16SrDNA ,对其测序后输入GenBank中与已知序列进行比较。结果 应用 16SrDNA序列同源性分析方法可对因受放射线影响 ,糖发酵特征发生改变而无法通过生化试验进行鉴定的菌株做出准确鉴定。结论 在无法通过生化试验方法对细菌作出准确鉴定时 。 展开更多
关键词 16S rDNA序列同源性分析 鉴定 放射线照射 口腔链球菌 放射治疗 鼻咽癌
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2株间日疟原虫18SrDNA的克隆及其同源性分析 被引量:1
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作者 高世同 李晓恒 +4 位作者 耿艺介 黄达娜 谢旭 梅树江 张仁利 《国际医学寄生虫病杂志》 CAS 2013年第6期317-320,共4页
目的克隆间日疟原虫河南分离株与湖北分离株红内期18SrDNA,并进行同源性分析。方法采用PCR方法从间日疟患者血样DNA中扩增间日疟原虫18SrDNA,纯化后与pGEM.Teasy质粒连接,转化大肠埃希氏菌JMl09;阳性克隆质粒经双酶切鉴定后,进行... 目的克隆间日疟原虫河南分离株与湖北分离株红内期18SrDNA,并进行同源性分析。方法采用PCR方法从间日疟患者血样DNA中扩增间日疟原虫18SrDNA,纯化后与pGEM.Teasy质粒连接,转化大肠埃希氏菌JMl09;阳性克隆质粒经双酶切鉴定后,进行序列测定,采用BLAST和MEGA4生物软件分析同源性。结果间日疟原虫18SrDNA扩增片段大小为998bp:阳性克隆重组质粒经双酶切鉴定,与预期结果相符;序列测定结果显示,河南、湖北2分离株间日疟原虫18SrDNA序列完全相同.与GenBank中报道的12株间日疟原虫相同序列进行比对,其同源性均大于99%:用邻位连接法(neigh—bor-joining,NJ)和非加权组平均法(UPGMA)2种方法构建系统发生树发现,河南分离株、湖北分离株与间日疟原虫X13926.1株遗传距离小.同属一个分支。结论克隆了间日疟原虫河南与湖北分离株红内期18SrDNA,该基因序列在不同地理株间遗传稳定。 展开更多
关键词 间日疟原虫 18SrDNA 序列同源性分析
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昆虫质多角体病毒研究的若干新进展 被引量:9
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作者 洪靖君 彭辉银 段家龙 《昆虫学报》 CAS CSCD 北大核心 2002年第6期815-821,共7页
质多角体病毒隶属呼肠孤病毒科质多角体病毒属 ,病毒粒子为二十面体球形颗粒 ,具有 3~ 5种结构蛋白 ,基因组由10或 11个节段双链RNA构成。按病毒基因组RNA片段在聚丙烯酰胺或琼脂糖凝胶中电泳图谱的差异 ,将质多角体病毒分为 15个电泳... 质多角体病毒隶属呼肠孤病毒科质多角体病毒属 ,病毒粒子为二十面体球形颗粒 ,具有 3~ 5种结构蛋白 ,基因组由10或 11个节段双链RNA构成。按病毒基因组RNA片段在聚丙烯酰胺或琼脂糖凝胶中电泳图谱的差异 ,将质多角体病毒分为 15个电泳型。随着RNA病毒序列测定策略的逐步成熟与完善 ,质多角体病毒的序列测定方面取得一定的进展 ,家蚕质多角体病毒 1的两个毒株 (H株和I株 ) ,舞毒蛾质多角体病毒 1和 14 ,及粉纹夜蛾质多角体病毒 15的基因组全序列得到了测定 ,但质多角体病毒的进化与起源的研究因缺乏足够的遗传信息仍受到限制。 展开更多
关键词 昆虫质多角体病毒 双链RNA 电泳型 序列同源性分析 研究进展
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朱砂叶螨HSP90基因克隆及原核表达 被引量:2
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作者 冯宏祖 刘映红 +3 位作者 何林 李明 卢文才 薛传华 《昆虫学报》 CAS CSCD 北大核心 2009年第8期845-851,共7页
采用RT-PCR及RACE技术克隆朱砂叶螨Tetranychus cinnabarinus的热激蛋白90(HSP90)基因,并进行序列分析,得到一条长2595bp的cDNA序列,该序列开放阅读框(open reading frame,ORF)为2169bp,编码722个氨基酸,分子量约为83.45kDa,理论等电点... 采用RT-PCR及RACE技术克隆朱砂叶螨Tetranychus cinnabarinus的热激蛋白90(HSP90)基因,并进行序列分析,得到一条长2595bp的cDNA序列,该序列开放阅读框(open reading frame,ORF)为2169bp,编码722个氨基酸,分子量约为83.45kDa,理论等电点为4.81,3′非编码区(untranslated region,UTR)为249bp,5′UTR为177bp。通过Antheprot分析发现5个HSP90家族的签名序列及胞质HSP90特征序列MEEVD。同源性分析表明,朱砂叶螨HSP90编码区核苷酸序列和其他已知的HSP90,尤其是节肢动物昆虫的HSP90,具有很高的相似性。将鉴定正确的原核重组表达质粒pET43a-TcHSP90,转化大肠杆菌Escherichia coli BL21(origami)进行原核表达,应用SDS-PAGE和Western blotting技术分离并检测融合蛋白,结果表明构建的原核表达质粒可以在宿主菌中稳定、正确表达。朱砂叶螨TcHSP90基因的克隆、原核表达,为进一步研究HSP90的性质和功能的研究提供有用的实验材料。 展开更多
关键词 朱砂叶螨 热激蛋白90 基因克隆 序列同源性分析 原核表达
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对巴通体及其所致疾病的新认识 被引量:5
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作者 翁心华 朱利平 《国外医学(微生物学分册)》 2004年第2期39-40,共2页
早在1907年,秘鲁科学家Alberto Barton首次在Carrion病患者红细胞内发现杆菌状致病性病原体,后将其命名为杆菌状巴通体(Bartonella bacilli-formis),其所引起的疾病称之为巴通体病(bartonel-losis).长期以来,杆菌状巴通体被认为是巴通... 早在1907年,秘鲁科学家Alberto Barton首次在Carrion病患者红细胞内发现杆菌状致病性病原体,后将其命名为杆菌状巴通体(Bartonella bacilli-formis),其所引起的疾病称之为巴通体病(bartonel-losis).长期以来,杆菌状巴通体被认为是巴通体属中唯一的一种病原体.在其分类上,<伯杰系统细菌学分类手册>中将巴通体科、立克次体科和无形体科归属为立克次体目.其中,巴通体科包括巴通体属和格雷汉体属(Grahamella).巴通体属仅有杆菌状巴通体1个种,格雷汉体属有2个种,分别为G-tal-pae和G.peromysci;立克次体科包括罗卡利马属(Rochalimaea)、立克次体属和柯克斯体属,其中罗卡利马属有2个种,分别为R.quintana和R.vinsonii,但在1992年又新增2个种,即R.henselae和R.eliza-bethae. 展开更多
关键词 巴通体 致病性病原体 巴通体病 分子鉴定 分子流行病学 基因序列同源性分析
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反相液相色谱-串联质谱法筛选牙鲆鱼蛋白质中潜在的过敏原 被引量:2
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作者 张晶宇 翟子扬 +2 位作者 顾盼 赵前程 祁艳霞 《食品安全质量检测学报》 CAS 2019年第7期1797-1803,共7页
目的建立反相液相色谱-串联质谱法(reversed phase liquid chromatography coupled with tandem mass spectrometry, RPLC-MS/MS)筛选牙鲆鱼(Paralichthys olivaceus)中潜在过敏原。方法采用RPLC-MS/MS技术对牙鲆鱼的蛋白质样品进行蛋... 目的建立反相液相色谱-串联质谱法(reversed phase liquid chromatography coupled with tandem mass spectrometry, RPLC-MS/MS)筛选牙鲆鱼(Paralichthys olivaceus)中潜在过敏原。方法采用RPLC-MS/MS技术对牙鲆鱼的蛋白质样品进行蛋白质组学分析。再将牙鲆鱼蛋白质样品在体外模拟胃液中消化,通过十二烷基硫酸钠-聚丙烯酰胺凝胶(sodium dodecyl sulfate-polyacrylamide gel electrophoresis, SDS-PAGE)电泳观察不同酶解时间下鱼蛋白的酶解情况,将耐酶解的蛋白通过胶内酶解处理后采用RPLC-MS/MS法进行分析。最后将鉴定到的蛋白质与已知过敏原进行序列同源性分析。结果在SDS-PAGE中酶解时间为3 h时位于40 kDa处的条带仍清晰可见,此处的蛋白为耐酶解的蛋白质,经胶内酶解后共鉴定到5种蛋白质。与已知过敏原蛋白进行蛋白序列同源性分析,牙鲆鱼的原肌球蛋白alpha-1与已知过敏原Ore m4的序列相似度较高。2种蛋白质的一致性和相似性分别为96.5%和97.9%。甘油醛-3-磷酸脱氢酶与已知过敏原Tri a 34序列对比一致性和相似性分别为72%和83%。肌酸激酶1与已知过敏原Penm2序列对比的一致性和相似性分别为42%和63%,2组序列相似度大于35%,说明也具有相似性。结论耐胃蛋白酶酶解的大部分蛋白质是潜在的过敏原,其序列与其他物种已知的蛋白过敏原高度相似。该方法可作为筛选食物中潜在过敏原的一种新方法。 展开更多
关键词 牙鲆鱼 过敏原 液相色谱-串联质谱法 序列同源性分析
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肠道病毒71型福建分离株(FJ08089)全基因组序列分析
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作者 吴冰珊 沈晓娜 +4 位作者 王美爱 王金章 谢剑锋 陈炜 严延生 《海峡预防医学杂志》 CAS 2010年第6期10-12,共3页
[目的]分析2008年福建省手足口病患儿标本肠道病毒71型(EV71)分离株FJ08089全基因组序列特征。[方法]应用RD细胞,从患者疱疹液标本分离EV71,用RT-PCR方法扩增分离株病毒的全基因组,分析其基因组特征。[结果]FJ08089株的基因组长度为7 40... [目的]分析2008年福建省手足口病患儿标本肠道病毒71型(EV71)分离株FJ08089全基因组序列特征。[方法]应用RD细胞,从患者疱疹液标本分离EV71,用RT-PCR方法扩增分离株病毒的全基因组,分析其基因组特征。[结果]FJ08089株的基因组长度为7 404 bp,其中包括5′端非编码区(5′UTR)长743 bp,病毒基因组编码区(ORF)全长6 576个核苷酸及3′端非编码区(3′UTR)长81 bp。ORF编码含2 192个氨基酸残基的多聚蛋白。[结论]FJ08089株基因组的结构与安徽地方株ANHUI703814十分相近,整个基因组的核苷酸同源性为93.8%,氨基酸同源性为92.6%,均属于C4亚型,而与Cox.A16国际标准株G10(U05876)差别较大,两者核苷酸同源性仅为77.9%,氨基酸同源性为84.0%。 展开更多
关键词 肠道病毒71型 基因组 手足口病 同源性序列分析
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Molecular Characterization of Viral G Gene in Emerging and Re-emerging Areas of Rabies in China, 2007 to 2011 被引量:20
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作者 Shu-LinLang Xiao—YanTao +5 位作者 Zhen-YangGuo QingTang HaoLi Cui.PingYin YingLi Guo—DongLiang 《Virologica Sinica》 SCIE CAS CSCD 2012年第3期194-203,共10页
In recent years (2007 to 2011), although the overall number of rabies cases in China has decreased, there is evidence of emerging or re-emerging cases in regions without previous rabies cases or with low incidence of ... In recent years (2007 to 2011), although the overall number of rabies cases in China has decreased, there is evidence of emerging or re-emerging cases in regions without previous rabies cases or with low incidence of rabies. To investigate the origin and the factors affecting the spread of rabies in China, specimens were collected from 2007 to 2011 from provinces with emerging and re-emerging cases and tested for the presence of the rabies virus. Positive specimens were combined with sequences from GenBank to perform comparisons of homology and functional sites, and to carry out phylogenetic analyses. Out of these regions, five provinces had 9 positive specimens from canine and cattle, and 34 canine or human specimens were obtained from previously high-incidence provinces. Complete sequences of G gene were obtained for these samples. Homology of the sequences of these 43 specimens was 87%-100% at the nucleotide level and 93.7% -100% at the amino acid level. These G gene sequences were combined with reference sequence from GenBank and used to construct a phylogenetic tree. The results showed that 43 specimens were all assigned to China clade I and clade II, with all specimens from emerging and re-emerging areas placed within clade I. Specimens isolated from Shanxi and Inner Mongolia in 2011 were distinct from previously-isolated local strains and had closer homology to strains from Hebei, Beijing and Tianjin whereas new isolates from Shanghai were tightly clustered with strains isolated in the 1990s. Finally, Shaanxi isolates were clustered with strains from adjacent Sichuan. Our results suggest that the rabies cases in emerging and re-emerging areas in China in the last 5 years are a consequence of the epidemic spreading from of neighboring provinces and regions experiencing a serious epidemic of rabies. 展开更多
关键词 Rabies virus G gene Genetic variation Molecular characteristics
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The Characteristics of vasa Gene from Japanese Sea Bass(Lateolabrax japonicas) and Its Response to the External Hormones 被引量:1
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作者 CHI Meili WEN Haishen +3 位作者 NI Meng QIAN Kun ZHANG Pei CHAI Senhao 《Journal of Ocean University of China》 SCIE CAS 2015年第4期717-723,共7页
The RNA helicase Vasa is an important regulator of primordial germ cell development. Its function in mature fish, espe- cially the hormone-related differences in maturing male fish has seldom been documented. In this ... The RNA helicase Vasa is an important regulator of primordial germ cell development. Its function in mature fish, espe- cially the hormone-related differences in maturing male fish has seldom been documented. In this study, a full length cDNA sequence of the vasa gene was cloned from Japanese sea bass, Lateolabraxjaponicas, and it was namedjsb-vasa. Homology analysis showed thatjsb-vasa was closely related to its teleost homologs. The spatial distribution ofjsb-vasa indicated that it was only highly ex- pressed in testis, showing its germ cell-specific expression pattern. During the testicular development cycle, jsb-vasa was highly expressed during early period of spermatogenesis, and reduced when spermatogenesis advanced. In addition, the jsb-vasa gene ex- pression was significantly inhibited at 6 h, 12 h and 24 h after injecting hCG (human ehorionic gonadotropin) and GnRHa (Gonad- otropin-releasing hormone analogue), indicating thatjsb-vasa gene may play an important role in spermatogenesis of Japanese sea bass, and be under the regulation of external sex hormones. 展开更多
关键词 vasa gene Japanese sea bass hCG/GnRHa treatment SPERMATOGENESIS
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Characterization of the Xenopus homolog of animmediate early gene associated with cell activation: sequence analysis and regulation of its expression by thyroid hormone during amphibian metamorphosis
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作者 VIVIACTLIANG TIFFANYSEDGWICK 《Cell Research》 SCIE CAS CSCD 1997年第2期179-193,共15页
The complex transformation of a tadpole to a frogduring amphibian development is under the control of thyroid hormone (T3). T3 is known to regulate gene transcription through its nuclear receptors. We have previouslyi... The complex transformation of a tadpole to a frogduring amphibian development is under the control of thyroid hormone (T3). T3 is known to regulate gene transcription through its nuclear receptors. We have previouslyisolated many genes which are up-regulated by T3 in theintestine of Xenopus laevis tadpoles. We have now cloneda full- length cDNA for one such gene (IU12). Sequenceanalysis shows that the IU12 cDNA encodes a plasmamembrane protein with 12 transmembrane domains andhomologous to a mammalian gene associated with cell activation and organ development. Similarly, we have foundthat IU12 is activated during intestinal remodeling whenboth cell death and proliferation take place. Furthermore,IU12 is an early T3-response gene and its expression in theintestine during T3-induced metamorphosis mimics thatduring normal development. These results argue for a roleof IU12 in the signal transduction pathways leading to intestinal metamorphosis. 展开更多
关键词 Thyroid hormone Xenopus laevis cell proliferation ORGANOGENESIS transcription factor
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鼠伤寒沙门氏菌purB受purR调控的实验证据
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作者 张海宁 黄谊 +1 位作者 秦浚川 王敖全 《科学通报》 EI CAS CSCD 北大核心 2001年第2期145-149,共5页
通过遗传图和序列同源性分析获得了鼠伤寒沙门氏菌purB核苷酸序列. 为揭示鼠伤寒沙门氏菌purB是否受purR调控, 对purB基因的PUR box进行了功能分析. PCR扩增野生型PUR box和其第14位保守碱基发生突变(C→T)的DNA片段, 分别与从鼠伤寒沙... 通过遗传图和序列同源性分析获得了鼠伤寒沙门氏菌purB核苷酸序列. 为揭示鼠伤寒沙门氏菌purB是否受purR调控, 对purB基因的PUR box进行了功能分析. PCR扩增野生型PUR box和其第14位保守碱基发生突变(C→T)的DNA片段, 分别与从鼠伤寒沙门氏菌野生型菌株LT2提取的PurR粗制品进行了凝胶阻滞实验. 结果表明, purB基因的PUR box与PurR阻遏蛋白有很好的结合能力, 而突变的PUR box则不能与PurR阻遏蛋白结合. 可见, 野生型鼠伤寒沙门氏菌purB与嘌呤从头合成途径中其他结构基因一样是受purR基因协同调控的. 此外还对不受调控的实验现象的机制做了研究. 结果表明purB组成型表达是purB∷MudJ基因融合发生在PUR box上游(-554 bp)的结果. 这一结果还为鼠伤寒沙门氏菌purB基因与其上游ycfC基因属于同一个操纵子提供了有力的证据. 展开更多
关键词 鼠伤寒沙门氏菌 PURB 序列同源性分析 PURBOX PU
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CLONING AND COMPARISON OF THE GENES ENCODING PREPROAPAMIN FROM THE VENOM OF 2 HONEYBEE AND 4 WASP SPECIES 被引量:3
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作者 张素方 施婉君 +1 位作者 程家安 张传溪 《Entomologia Sinica》 CSCD 2003年第1期21-26,共6页
Preproapamin genes were amplified by RT-PCR from total RNA from the venom glands of 2 honeybee species, Apis mellifera, A. cerana cerana, and 4 wasp species, Vespa magnifica, V. velutina nigrothorax and Polistes hebra... Preproapamin genes were amplified by RT-PCR from total RNA from the venom glands of 2 honeybee species, Apis mellifera, A. cerana cerana, and 4 wasp species, Vespa magnifica, V. velutina nigrothorax and Polistes hebraeus, respectively. Their PCR products were ligated into pGEM -T easy vector and the nucleotide sequences analyzed. The six fragments were all 141?bp in length and contained a n ORF coding the precursor of apamin. The apamin precursors of V. magnifica, V. velutina nigrothorax and P. hebraeus had 95% and 93% similarity with that of A. melliera in nucleotide and amino acid sequences, respectively. That of Vespu la maculifrons was identical to that of A. mellifera in nucleotide and amino acid sequences. Apamin precursors of V. magnifica, P. hebraeus and V. velutina nigrothorax also had the same nucleotide sequences. The nucleotide sequences o f preproapamin genes from the Chinese honeybee, A. cerana cerana and 4 wasp sp ecies are described for the first time. A notable discovery was that the wasps species had exactly same apamins as the honeybees despite the fact they belong to different insect families. 展开更多
关键词 VENOM preproapamin APAMIN sequence comparison HONEYBEE WASP
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