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Analysis of Saccharina japonica transcriptome using the high-throughput DNA sequencing technique and its vanadium-dependent haloperoxidase gene 被引量:1
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作者 LIANG Xiayuan WANG Xumin +6 位作者 CHI Shan WU Shuangxiu SUN Jing LIU Cui CHEN Shengping YU Jun LIU Tao 《Acta Oceanologica Sinica》 SCIE CAS CSCD 2014年第2期27-36,共10页
Saccharina is one of the most important cold-water living marine brown algal genera. In this study we ana-lyzed the transcriptome of S. japonica, which belongs to the 1 000 Plants (OneKP) Project, by using a next-ge... Saccharina is one of the most important cold-water living marine brown algal genera. In this study we ana-lyzed the transcriptome of S. japonica, which belongs to the 1 000 Plants (OneKP) Project, by using a next-generation high-throughput DNA sequencing technique. About 5.16 GB of raw data were generated, and 65 536 scaffolds with an average length of 454 bp were assembled with SOAP de novo assembly method. In total, 19 040 unigenes were identified by BLAST;25 734 scaffolds were clustered into 37 Gene ontology functional groups;6 760 scaffolds were classified into 25 COG categories, as well as 2 665 scaffolds that were assigned to 306 KEGG pathways. Majority of the unigenes exhibited more similarities to algae including brown algae and diatom than other cyanobacteria, marine diatom, and plant. Saccharina japonica has the outstanding capability to accumulate halogen such as Br and I via halogenation processes from seawater. We acquired 42 different vanadium-dependent haloperoxidases (vHPO) in S. japonica transcriptome data, including 5 segments of vanadium-dependent iodoperoxidase (vIPO) and 37 segments of vanadium-de-pendent bromoperoxidase (vBPO). Complicated analyses of identified fulllength S. japonica vBPO1 and S. japonica vBPO2 revealed the importance of vBPO among species of brown algae and the strong relationship between marine algal vBPOs and vIPOs. This study will enhance our understanding of the biological charac-teristics and economic values of S. japonica species. 展开更多
关键词 Saccharina japonica transcriptomic sequencing vanadium-dependent haloperoxidase phylogenic analysis
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Vanadium Haloperoxidases Model Compounds: Synthesis, Structural Characterization and Mimic Catalytic Bromination Activity of [VO(C_2O_4)(2,2′-bipy)(H_2O)]·C_2H_5OH and VO(C_2O_4)(phen)(H_2O) 被引量:1
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作者 REN Dong-xue CAO Yun-zhu +1 位作者 CHEN Chen XING Yong-heng 《Chemical Research in Chinese Universities》 SCIE CAS CSCD 2012年第5期768-774,共7页
Two oxo-vanadium(IV) complexes, [VO(C2O4)(2,2′-bipy)(H2O)]·C2H5OH(1) and VO(C2O4)(phen)(H2O) (2), where 2,2′-bipy=2,2′-bipyridyl, phen=1,10-phenanthroline, were synthesized as potential funct... Two oxo-vanadium(IV) complexes, [VO(C2O4)(2,2′-bipy)(H2O)]·C2H5OH(1) and VO(C2O4)(phen)(H2O) (2), where 2,2′-bipy=2,2′-bipyridyl, phen=1,10-phenanthroline, were synthesized as potential functional models of vanadium haloperoxidases(VHPOs) in mixed solvent of ethanol and water at room temperature. The complexes were characterized by elemental analysis, infrared(IR), UV-Vis and X-ray crystallography. Structural analyses showed that vanadium atom was coordinated by a terminal oxygen, one oxygen atom from coordinated water, two oxygen atoms from the carboxylate group of oxalic acid, and two nitrogen atoms(N1 and N2) from 2,2′-bipy/phen. Central vanadium atoms in complexes 1 and 2 were both in a distorted-octahedral environment, and some intermolecular hydrogen bonding linkages were also observed in each complex. Bromination reaction activity of the two complexes was evaluated with phenol red as organic substrate in the presence of H2O2, Br-and phosphate buffer, indicating that they can be considered as a potential functional model of VHPO. In addition, thermal analysis was also performed and discussed in detail. 展开更多
关键词 Oxo-vanadium complex Bromination reaction activity Vanadium haloperoxidase
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东方拟无枝酸菌中vcm14基因的敲除对万古霉素合成的影响 被引量:2
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作者 李航 魏维 +3 位作者 阮林高 李秋爽 陈代杰 罗敏玉 《中国抗生素杂志》 CAS CSCD 北大核心 2009年第6期329-332,共4页
PCR-targeting是一种用于敲除或阻断放线菌染色体上某一基因的快速高效的方法。本研究利用该方法在大肠埃希菌中构建破坏粘粒cLYLH17(Δvcm14::apr),通过结合转移首次敲除东方拟无枝酸菌HCCB10007中万古霉素生物合成基因簇中推测的halop... PCR-targeting是一种用于敲除或阻断放线菌染色体上某一基因的快速高效的方法。本研究利用该方法在大肠埃希菌中构建破坏粘粒cLYLH17(Δvcm14::apr),通过结合转移首次敲除东方拟无枝酸菌HCCB10007中万古霉素生物合成基因簇中推测的haloperoxidase基因——vcm14,得到一株双交换阻断突变株A.orientalis dvcm14(Δvcm14::apr)。该菌不产生万古霉素及其类似物,证实vcm14基因的编码蛋白不是haloperoxidase,且该蛋白不参与万古霉素的卤化反应,可能是万古霉素生物合成途径中的一个关键酶。本研究为阐明万古霉素生物合成途径中的卤化过程提供了有益线索。 展开更多
关键词 万古霉素 PCR—targeting 基因敲除 haloperoxidase
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