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Molecular cloning, characterization and expression analysis of a catalase gene in Paphia textile 被引量:1
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作者 WU Xiangwei LI Jiakai +1 位作者 TAN Jing LIU Xiande 《Acta Oceanologica Sinica》 SCIE CAS CSCD 2016年第8期65-73,共9页
Catalase is an important antioxidant protein that can protect organisms against various forms of oxidative damage by eliminating hydrogen peroxide. In this study, the catalase c DNA of Paphia textile(Pt CAT) was clo... Catalase is an important antioxidant protein that can protect organisms against various forms of oxidative damage by eliminating hydrogen peroxide. In this study, the catalase c DNA of Paphia textile(Pt CAT) was cloned using RTPCR and rapid amplification of c DNA ends(RACE). Pt CAT is 1 921 bp long and consists of a 5′-UTR of 50 bp, a 3′-UTR of 349 bp, and an ORF of 1 542 bp that encodes 513 amino acids with a molecular weight of 58.4 k D and an estimated isoelectric point of 8.2. Sequence alignment indicated that Pt CAT contained a highly conserved catalytic signature motif(^(61)FNRERIPERVVHAKGAG^(77)), a proximal heme-ligand signature sequence(^(352)RLFSYSDP^(359)), and three catalytic amino acid residues(H^(72), N^(145), and Y^(356)). Pt CAT also contains two putative N-glycosylation sites(^(34)NKT^(36) and ^(437)NFT^(439)) and a peroxisome-targeting signal(^(511)AQL^(513)). Furthermore, Pt CAT shares 53%–88% identity and 29%–89% similarity with other catalase amino acid sequences. Pt CAT m RNA was present in all tested organs, including the heart, digestive gland, adductor muscle, gonad, gill, and mantle, but its expression was highest in the digestive gland. High-temperature-induced stress produced two expression patterns of Pt CAT m RNA: first, an initial up-regulation followed by a down-regulation in the heart, digestive gland, and gonad and, second, consistent down-regulation in all other organs. These results demonstrate that Pt CAT is a typical member of the catalase family and might be involved in the responses to harmful environmental factors. 展开更多
关键词 Paphia textile catalase(CAT) cloning sequence analysis expression analysis high temperature stress
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Molecular Cloning of Myostatin Partial cDNA of Beijing Duck and Its Expression in Breast Muscle 被引量:3
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作者 WANG Yong-sheng HOU Shui-sheng HUANG Wei KANG Jun-mei 《Agricultural Sciences in China》 CAS CSCD 2006年第6期468-472,共5页
In this experiment, 500 bp cDNA of myostatin gene was cloned from a Beijing duck's breast, The duck myostatin gene was found to have 98, 96, 95, 88, and 87% sequence similarity at the cDNA level with domestic goose, ... In this experiment, 500 bp cDNA of myostatin gene was cloned from a Beijing duck's breast, The duck myostatin gene was found to have 98, 96, 95, 88, and 87% sequence similarity at the cDNA level with domestic goose, chicken, domestic pigeon, human, and pig, respectively. The predicted amino acid sequence has an overall similarity with a comparable region of turkey 99%, domestic goose 98%, and chicken 99%. Conserved domains of deduced amino acids showed that it belonged to the TGF-beta family. Myostatin expression in breast muscle was higher at 28, 35, and 42 days than at 7, 14, and 21 days. The pattern of myostatin expression was closely parallel to the trend of breast muscle growth, suggesting that myostatin might play an important role in breast muscle development. It was possible to postulate that myostatin may be a major determinant of muscle mass in breast muscle, as shown in other species. 展开更多
关键词 Beijing duck MYOSTATIN cloning and sequence analysis EXPRESSION
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c D N Acloning and sequence analysis of hepatitis G virus genome isolatedfrom a Chinese blood donor 被引量:1
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作者 王海林 陈红松 +9 位作者 夏宁邵 谭文杰 陈刚 刘玉兰 丛郁 孙婧 曾定 侯云德 王宇 詹美云 《Chinese Medical Journal》 SCIE CAS CSCD 1999年第8期75-77,共3页
Objective To obtain full length sequence of a Chinese hepatitis G virus (HGV) strain (HGVch) and investigate the genetic characteristic of HGVch and its identity to other isolates Methods Reverse transcription (RT... Objective To obtain full length sequence of a Chinese hepatitis G virus (HGV) strain (HGVch) and investigate the genetic characteristic of HGVch and its identity to other isolates Methods Reverse transcription (RT) and nested PCR were used to screen HGV RNA positive serum and amplify cDNA fragments A positive serum without known hepatitis virus markers was selected for isolating HGV RNA template The HGV genome was divided into 12 overlapping fragments and directly cloned into pGEM T vector Sequences were determined by dideoxy terminus end method of DNA sequencing and then analyzed by computer Results The twelve fragments of HGVch cover 9213 nucleotides in length, containing a large open reading frame (ORF) encoding 2873 animo acids polyprotein that began with a methonine residue and ended at termination codon HGVch is about 86 5%-89 5% identical to other known HGV isolates at the nucleotide level and about 93 9%-96 2% at the deduced animo acid level Conclusion HGV is a non A E hepatitis causal agent, proved to be related with posttransfusion hepatitis in all over the world Chinese HGV isolate has very close relationship to other isolates from Africa, Europe, Japan, without significant difference across the entire genome It is suggested that the sequences of HGV isolates are very conservative and the evolution is very slow 展开更多
关键词 HGVch · cloning · sequence analysis
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Continuous desulfurization and bacterial community structure of an integrated bioreactor developed to treat SO_2 from a gas stream 被引量:6
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作者 Jian Lin Lin Li +2 位作者 Wenjie Ding Jingying Zhang Junxin Liu 《Journal of Environmental Sciences》 SCIE EI CAS CSCD 2015年第11期130-138,共9页
Sulfide dioxide(SO2) is often released during the combustion processes of fossil fuels. An integrated bioreactor with two sections, namely, a suspended zone(SZ) and immobilized zone(IZ), was applied to treat SO2... Sulfide dioxide(SO2) is often released during the combustion processes of fossil fuels. An integrated bioreactor with two sections, namely, a suspended zone(SZ) and immobilized zone(IZ), was applied to treat SO2 for 6 months. Sampling ports were set in both sections to investigate the performance and microbial characteristics of the integrated bioreactor. SO2 was effectively removed by the synergistic effect of the SZ and IZ, and more than 85%removal efficiency was achieved at steady state. The average elimination capacity of SO2 in the bioreactor was 2.80 g/(m3·hr) for the SZ and 1.50 g/(m3· hr) for the IZ. Most SO2 was eliminated in the SZ. The liquid level of the SZ and the water content ratio of the packing material in the IZ affected SO2 removal efficiency. The SZ served a key function not only in SO2 elimination, but also in moisture maintenance for the IZ. The desired water content in IZ could be feasibly maintained without any additional pre-humidification facilities. Clone libraries of 16 S r DNA directly amplified from the DNA of each sample were constructed and sequenced to analyze the community composition and diversity in the individual zones.The desulfurization bacteria dominated both zones. Paenibacillus sp. was present in both zones, whereas Ralstonia sp. existed only in the SZ. The transfer of SO2 to the SZ involved dissolution in the nutrient solution and biodegradation by the sulfur-oxidizing bacteria.This work presents a potential biological treatment method for waste gases containing hydrophilic compounds. 展开更多
关键词 Biological deodorization Integrated bioreactor Sulfur dioxide Sulfur bacteria DNA sequence analysis Clone library
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Difference in DNA sequences in SSU rDNA variable regions among pathogens isolated from different epidemic foci of visceral leishmaniasis in China
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作者 胡孝素 卜玲毅 +3 位作者 马莹 王雅静 敬保迁 易桃林 《Chinese Medical Journal》 SCIE CAS CSCD 2002年第10期17-19,143,共4页
To confirm the existence of point mutations in the SSU rDNA variable regions of 5 Leishmania donovani (L d ) isolates from different epidemic foci in China Methods Specific SSU rDNA fragments from nuclear DNA of 7... To confirm the existence of point mutations in the SSU rDNA variable regions of 5 Leishmania donovani (L d ) isolates from different epidemic foci in China Methods Specific SSU rDNA fragments from nuclear DNA of 7 Leishmania species/isolates were amplified by PCR and then cloned into pGEM R T Easy Vectors After that, the specific fragments were sequenced by an automated DNA sequencer Results Sequence analysis showed that the amplified DNA fragments of 7 Leishmania species/isolates were all 392 bp in length All 5 point mutations were located in two unique sequence blocks (UQ Ⅰ and UQ Ⅱ), and no insertions or deletions were found The identities of comparison of Leishmania in GeneBank were more than 98% Conclusion Five point mutations exist in the SSU rDNA variable region of 5 L d isolates from different epidemic foci of visceral leishmaniasis (VL) in China Sequence differences of the SSU rDNA variable region exist among L d isolates from different foci 展开更多
关键词 visceral leishmaniasis · Leishmania · point mutation · small subunit ribosomal DNA · polymerase chain reaction · cloning · sequence analysis · epidemic foci
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