1) 3D polymerase
3D聚合酶
1.
Three-dimensional structure modeling and functional analysis of 3D polymerase of foot-and-mouth disease virus strain AF72;
口蹄疫病毒AF72株3D聚合酶的三维结构模拟和功能分析
2) 3D polymerase gene
3D聚合酶基因
1.
The 3D polymerase gene of Foot-and-mouth disease virus strain AF72 was amplified by reverse transcription polymerase chain reaction(RT-PCR),The purified PCR products were cloned into pGEM-T easy Vectors,and the nucleotide sequences were highly homologous to other four reference strains from GenBank.
采用RT-PCR方法扩增口蹄疫病毒(FMDV)AF72株的3D聚合酶基因,并将其克隆至pGEM-T easy载体,测序分析结果表明,AF72 3D聚合酶基因与GenBank中公布的其他4个参考序列均具有较高的同源性。
3) Taq DNA polymerase
TaqDNA聚合酶
1.
coli DH5α was transformed with p Taq expressing plasmid within which the Taq DNA polymerase gene was inserted.
用含有TaqDNA聚合酶基因的 pTaq表达质粒转化E 。
4) Enzymatic polymerization
酶促聚合
1.
Novel Functional Block Copolymer Combining Enzymatic Polymerization and ATRP and Its Self-Assembly Behavior Study;
酶促聚合方法和ATRP方法结合制备新型功能嵌段共聚物及其自组装行为研究
5) Polyketide synthase
聚酮合酶
1.
Gene deletion vector pXL05 was used to disrupt oligomycin polyketide synthase (PKS) encoding genes(olmA) in Streptomyces a.
本研究以产阿维菌素B和寡霉素的阿维链霉菌CZ8-73为出发菌株,构建了基因缺失载体pXL05,并将其转入CZ8-73中,通过缺失载体和染色体之间的同源双交换,对染色体上长达90kb的寡霉素聚酮合酶(PKS)基因簇(olmA)进行了缺失。
2.
The recombinant Sorangium cellulosum in which the epoK gene has been inactivated by random mutagenesis and so produces only epothilone D and C,does not produce epothilone A or B,duo to an alteration in the genes coding for the epothilone polyketide synthase(PKS).
重组纤维堆囊菌的epoK基因因随机诱变而失活,由于埃博霉素聚酮合酶(PKS)基因编码的改变,生产菌株只产生埃博霉素D和C,而不产生埃博霉素A和B。
3.
OBJECTIVE To clone and characterize type Ⅲ polyketide synthases (PKSs) gene from Fallopia multiflora.
目的克隆并表征中药材何首乌(Fallopia multiflora)中的Ⅲ型聚酮合酶(polyketide synthases,PKS)基因。
6) RNA polymerase
RNA聚合酶
1.
Subcloning and expression of influenza virus RNA polymerase PB1-1 fragment;
流感病毒RNA聚合酶PB1-1亚基片段的克隆及表达
2.
Isolation and purification of RNA polymerase from influenza virus;
流感病毒RNA聚合酶的分离与纯化(英文)
3.
Stringent RNA polymerase of E. coli and its in vivo transcriptional activity;
大肠杆菌严谨型RNA聚合酶的筛选及体内转录活性测定
补充资料:DNA聚合酶I
分子式:
CAS号:
性质: 一般认为参与DNA损伤的修复(在切割修复中的修复复制阶段和切除阶段),它由一条多肽链(大约1000个氨基酸,分子量109 000)组成,具有外切酶活性,合成速率为每秒17个核苷酸,每个细菌细胞大约含有400个这样的酶分子。
CAS号:
性质: 一般认为参与DNA损伤的修复(在切割修复中的修复复制阶段和切除阶段),它由一条多肽链(大约1000个氨基酸,分子量109 000)组成,具有外切酶活性,合成速率为每秒17个核苷酸,每个细菌细胞大约含有400个这样的酶分子。
说明:补充资料仅用于学习参考,请勿用于其它任何用途。
参考词条