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光合细菌Rhodobacter sphaeroides glnBlacZ 融合子的构建与表达 被引量:1
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作者 梁莉 朱美珍 吴永强 《植物生理学报(0257-4829)》 CSCD 1999年第3期249-255,共7页
亚克隆了Rhodobacter sphaeroides glnB启动子,以pMP220 为载体构建成glnBlacZ融合子。将glnBlacZ、nifHlacZ、nifAlacZ分别导入R. sphaeroide... 亚克隆了Rhodobacter sphaeroides glnB启动子,以pMP220 为载体构建成glnBlacZ融合子。将glnBlacZ、nifHlacZ、nifAlacZ分别导入R. sphaeroides 谷氨酸合酶突变株gltB- 、gltD- 和野生型菌株中,分析了突变对固氮基因转录表达的影响。试验证明,在gltBD 突变株中nifH 的表达受阻遏,nifA 表达水平很低。这证明glt 基因的突变引起固氮酶结构基因和固氮正调节基因的转录被阻遏,而glnB 基因的表达几乎不受影响。试验还测定了环境中结合态氮和有机酸等信号分子对glnB 和nifH 表达的影响,发现加入氨或谷氨酰胺后,nifH 的表达受到明显的阻遏作用,glnBlacZ的β半乳糖苷酶活性虽下降30 % 左右但不随结合态氮浓度升高而变化,仍维持在一个较高的水平。α酮戊二酸和丙酮酸对nifH 展开更多
关键词 浑球红细菌 blnB-lacZ 融合子 glt变种
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巴西固氮螺菌Yu62 glnB基因的克隆及其功能分析
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作者 李周华 陈三凤 李季伦 《Acta Genetica Sinica》 SCIE CAS CSCD 北大核心 2001年第10期964-970,共7页
通过原位杂交从巴西固氮螺菌Yu62的基因文库中 ,筛选到glnB基因的阳性克隆 ,将3 7kb/EcoRI+PstI的阳性克隆亚克隆到pUC1 9中 ,进行了全序列分析 ,其在GenBank中的登记号是AF32 3960。DNA序列分析表明该阳性克隆含有完整的glnB基因 ,gln... 通过原位杂交从巴西固氮螺菌Yu62的基因文库中 ,筛选到glnB基因的阳性克隆 ,将3 7kb/EcoRI+PstI的阳性克隆亚克隆到pUC1 9中 ,进行了全序列分析 ,其在GenBank中的登记号是AF32 3960。DNA序列分析表明该阳性克隆含有完整的glnB基因 ,glnB基因下游是编码谷氨酰胺合成酶 (GS)的glnA基因 ,glnB基因上游是一个编码未知蛋白的ORF。glnB基因编码区长 336bp,编码 1 1 2个氨基酸 ,与肺炎克氏杆菌、大豆慢生根瘤菌、豌豆根瘤菌及大肠杆菌在氨基酸顺序的同源性分别高达 71 %、77%、79%和 69%。将卡那霉素抗性片段 (Km -cas sette)插入glnB基因的BglII位点 ,通过三亲杂交法将其引入到巴西固氮螺菌Yu62中 ,通过同源重组 ,获得GlnB- 突变株 (glnB ::Km)。为了进一步分析glnB基因的功能 ,将glnB基因的编码区 ( 339bp)构建在pVK1 0 0中 ,置于Km启动子下组成型表达 ,形成重组质粒pVK -II。将重组质粒pVK -II转入到GlnB- 突变株 ,构建成互补株C -glnB(glnB ::Km/glnB)。对GlnB-突变株和互补株的固氮酶活性和生长性能的测定表明 ,GlnB- 突变体无固氮酶活性 ,即表型为Nif- ;而互补株像野生型菌株一样具有固氮酶活性。突变株、互补株及野生型在菌落生长速度上基本相同。将含有glnB基因的重组质粒pVK -II分别转移到野生型Yu62? 展开更多
关键词 巴西固氮螺菌YU62 glnb基因 PⅡ蛋白 glnb^-突变标 基因克隆 功能
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巴西固氮螺菌中P_Ⅱ和P_Z在固氮调节中的不同作用 被引量:1
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作者 陈三凤 管乐 +3 位作者 应娇妍 李周华 王娟 李季伦 《微生物学报》 CAS CSCD 北大核心 2001年第5期523-529,共7页
在巴西固氮螺菌 (Azospirillumbrasilense)中 ,glnB和glnZ是两个高度同源基因 ,分别位于 3 7kb EcoRI+PstI和 3 7kb SalI的两个不同的染色体片段上。用卡那霉素盒 (Kmr cas sette)插入法 ,对glnB和glnZ分别进行定位诱变 ,并获得相应的... 在巴西固氮螺菌 (Azospirillumbrasilense)中 ,glnB和glnZ是两个高度同源基因 ,分别位于 3 7kb EcoRI+PstI和 3 7kb SalI的两个不同的染色体片段上。用卡那霉素盒 (Kmr cas sette)插入法 ,对glnB和glnZ分别进行定位诱变 ,并获得相应的突变株 ,即glnB- 和glnZ- 。研究表明 ,glnB- 突变株丧失固氮酶活性 ,表现为Nif- ,而glnZ- 象野生型菌株一样具有固氮酶活性。为了进一步研究这两个基因的功能 ,将glnB和glnZ分别构建在pVK1 0 0载体上形成重组质粒pVK -Ⅱ和pVK -Z ,对glnB- 和glnZ- 突变株进行互补实验 ,进一步证明了glnB与固氮酶活有直接相关性 ,而glnZ无此作用。同时 ,通过三亲接合法将pVK -Ⅱ和pVK -Z分别转移到巴西固氮螺菌野生型Yu62和具有一定抗铵能力的draT- 突变株中 ,使glnB和glnZ的拷贝数增加 ,进一步比较它们的固氮酶活性。结果表明多拷贝的glnB基因 ,能显著提高固氮酶活性 ,而多拷贝的glnZ对固氮酶活性无影响。同时 ,将pVK Ⅱ和pVK -Z分别转移到nifA- 突变株中 ,结果表明glnB和glnZ均不能恢复nifA- 展开更多
关键词 巴西固氮螺菌 glnb基因 glnZ基因 突变株 固氮酶活性
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African Swine Fever Virus MGF-110-9L-deficient Mutant Has Attenuated Virulence in Pigs 被引量:13
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作者 Dan Li Yinguang Liu +6 位作者 Xiaolan Qi Yuan Wen Pan Li Zhao Ma Yongjie Liu Haixue Zheng Zhijie Liu 《Virologica Sinica》 SCIE CAS CSCD 2021年第2期187-195,共9页
African swine fever virus(ASFV)is the etiological agent of African swine fever(ASF),an often lethal disease in domestic and wild pigs.ASF represents a major threat to the swine industry worldwide.Currently,no commerci... African swine fever virus(ASFV)is the etiological agent of African swine fever(ASF),an often lethal disease in domestic and wild pigs.ASF represents a major threat to the swine industry worldwide.Currently,no commercial vaccine is available because of the complexity of ASFV or biosecurity concerns.Live attenuated viruses that are naturally isolated or genetically manipulated have demonstrated reliable protection against homologous ASFV strain challenge.In the present study,a mutant ASFV strain with the deletion of ASFV MGF-110-9L(ASFV-D9L)was generated from a highly virulent ASFV CN/GS/2018 parental strain,a genotypeⅡASFV.Relative to the parental ASFV isolate,deletion of the MGF-110-9L gene significantly decreased the ability of ASFV-D9L to replicate in vitro in primary swine macrophage cell cultures.The majority of animals inoculated intramuscularly with a low dose of ASFV-D9L(10 HAD50)remained clinically normal during the 21-day observational period.Three of five ASFV-D9L-infected animals displayed low viremia titers and low virus shedding and developed a strong virus-specific antibody response,indicating partial attenuation of the ASFV-D9L strain in pigs.The findings imply the potential usefulness of the ASFV-D9L strain for further development of ASF control measures. 展开更多
关键词 African swine fever virus(ASFV) MGF-110-9L mutant Attenuated virulence PIG
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Crystallization of Nitrogenase MoFe Protein (NifB Av1) from a nifB Mutated Strain UW45 of Azotobacter vinelandii
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作者 赵颖 吕玉兵 +4 位作者 赵剑峰 周军贤 潜忠兴 王耀萍 黄巨富 《Acta Botanica Sinica》 CSCD 2003年第7期820-824,共5页
Six hundred and 28 mg of NifB(-) Av1 was obtained by a chromatography twice on DE 52 columns and Sephacryl S-300 column from the crude extract (37 677 mg) of a nifB mutated strain UW45 of Azotobacter vinelandii Lipman... Six hundred and 28 mg of NifB(-) Av1 was obtained by a chromatography twice on DE 52 columns and Sephacryl S-300 column from the crude extract (37 677 mg) of a nifB mutated strain UW45 of Azotobacter vinelandii Lipmann. The protein was almost homogeneous as determined by Coomassie staining of SDS gels. The analysis by SDS-PAGE showed that NifB(-)Av1 was similar to Av1 from wild-type strain of A. vinelandii (OP) in the kinds of subunits (alpha and beta subunit). When complemented with Av2, NifB(-)Av1 had hardly any H-reducing activity, but could be significantly activated by FeMoco extracted from Av1. Under a suitable condition for crystallization, short dark-brown rhombohedral crystals could be obtained from NifB(-)Av1. Both of the longest sides of the biggest crystal were 0.1 mm. The time of the formation of crystals and number, size, quality and shape of crystals obviously depended not only on the kinds and concentrations of the components in the precipitant solution, but also on the methods for crystallization and technical bias, etc. The preliminary results showed that the crystal seemed to be formed from NifB(-)Av1. 展开更多
关键词 mutant strain UW45 of Azotobacter vinelandii nitrogenase NifB(-)Av1 CRYSTALLIZATION
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Cancer-derived C-terminus-extended p53 mutation confers dominant-negative effect on its wild-type counterpart
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作者 Shibo Huang Bo Cao +6 位作者 Jieqiong Wang Yiwei Zhang Elisa Ledet Oliver Sartor Yuqin Xiong Shelya X.Zeng Hua Lu 《Journal of Molecular Cell Biology》 SCIE CAS CSCD 2022年第1期11-20,共10页
The vast majority of p53 missense mutants lose the wild-type (wt) function and/or exert ‘dominant-negative’ effects on their wt counterpart. Here, we identify a novel form of p53 mutation with an extended C-terminus... The vast majority of p53 missense mutants lose the wild-type (wt) function and/or exert ‘dominant-negative’ effects on their wt counterpart. Here, we identify a novel form of p53 mutation with an extended C-terminus (p53 long C-terminus, p53LC) in a variety of human cancers. Interestingly, the two representative mutants (named ‘p53-374*48’ and ‘p53-393*78’) as tested in this study show both loss-of-function and dominant-negative phenotypes in cell proliferation and colony formation assays. Mechanistically, p53LCs interact with and retain wt p53 in the cytoplasm and prevent it from binding to the promoters of target genes, consequently inhibiting its transcriptional activity. Also, p53LCs are very stable, though not acetylated in cells. Remarkably, the p53LCs can desensitize wt p53-containing cancer cells to p53-activating agents. Together, our results unveil a longer form of p53 mutant that possesses a dominant-negative effect on its wt counterpart, besides losing its wt activity. 展开更多
关键词 mutant p53-393*78 mutant p53-374*48 P53 longer C-terminus p53 dominant-negative effect drug resistance ACETYLATION
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Chromatin architectural alterations due to null mutation of a major CG methylase in rice
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作者 Jinbin Wang Xiaochong Li +13 位作者 Qianli Dong Changping Li Juzuo Li Ning Li Baoxu Ding Xiaofei Wang Yanan Yu Tianya Wang Zhibin Zhang Yiyang Yu Man Lang Zixian Zeng Bao Liu Lei Gong 《Journal of Integrative Plant Biology》 SCIE CAS CSCD 2022年第12期2396-2410,共15页
Associations between 3D chromatin architectures and epigenetic modifications have been characterized in animals.However,any impact of DNA methylation on chromatin architecture in plants is understudied,which is confin... Associations between 3D chromatin architectures and epigenetic modifications have been characterized in animals.However,any impact of DNA methylation on chromatin architecture in plants is understudied,which is confined to Arabidopsis thaliana.Because plant species differ in genome size,composition,and overall chromatin packing,it is unclear to what extent findings from A.thaliana hold in other species.Moreover,the incomplete chromatin architectural profiles and the low-resolution high-throughput chromosome conformation capture(Hi-C)data from A.thaliana have hampered characterizing its subtle chromatin structures and their associations with DNA methylation.We constructed a high-resolution Hi-C interaction map for the null OsMET1-2(the major CG methyltransferase in rice)mutant(osmet1-2)and isogenic wild-type rice(WT).Chromatin structural changes occurred in osmetl-2,including intra-/inter-chromosomal interactions,compartment transition,and topologically associated domains(TAD)variations.Our findings provide novel insights into the potential function of DNA methylation in TAD formation in rice and confirmed DNA methylation plays similar essential roles in chromatin packing in A,thaliana and rice. 展开更多
关键词 3D chromatin architectures DNA methylation Hi-C osmet1-2 mutant
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