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peroxidase gene
    Effect of selenium on human myocardial glutathione peroxidase gene expression
    硒对人心肌谷胱甘肽过氧化物酶基因表达影响的研究
    The Sequence of Lycopersicon esculentum Thylakoid-Bound Ascorbate Peroxidase Gene TtAPX
    番茄类囊体膜抗坏血酸过氧化物酶基因TtAPX序列(英文)
    Effects of Waterlogging on Some Physiological and Biochemical Indexes of Transgenic Tobacco (Nicotiana tobacum L.) Lines with Superoxide Dismutase or Peroxidase Gene
    淹水对转超氧化物歧化酶或过氧化物酶基因烟草某些生理生化指标的影响
    Homologous Cloning of the 3′End of Cytosolic Ascorbate Peroxidase Gene(cAPX) from Dimocarpus longan Embryogenic Callus
    龙眼胚性愈伤组织胞浆型抗坏血酸过氧化物酶基因3'末端序列的同源克隆
    Intrauterine therapy of goitrous hypothyroidism in a boy with a new compound heterozygous mutation (Y453D and C800R) in the thyroid peroxidase gene: A long-term follow-up
    甲状腺过氧化物酶基因的一种新复合杂合型突变(Y453D和C800R)男胎甲状腺肿和甲状腺功能减退的宫内治疗:一项长期随访研究
    Fusion Expression and Preparation of Antibody of Ascorbate Peroxidase Gene from Chinese Wild Vitis Pseudoreticulata in E.coli
    中国华东葡萄抗坏血酸过氧化物酶基因的原核表达及抗体制备
    Relationship of phenylalanine ammonia lyase gene (PAL), cytosolic ascorbate peroxidase gene (apx) and peroxidase K gene (POX K) with resistance to Exserohilum turcicum in maize was analysed by PCR and RT-PCR, in which resistant and susceptible isolines of maize were used as experimental materials.
    以玉米抗、感大斑突脐孢菌近等基因系为材料 ,采用PCR和RT -PCR技术 ,初步研究了苯丙氨酸解氨酶基因 (PAL)、胞液抗坏血酸过氧化物酶基因 (apx)和过氧化物酶K基因 (POXK)等防卫基因与玉米对大斑病菌抗性的关系。
    The5' regulation sequence of wound-inducible peroxidase gene(tpoxN1)from tobacco was obtained using GenomeWalker. Sequence analysis demonstrated that the conservative sequence5' YTCAATCA at the tran scription start position(tspA)of tpoxN1gene was quite similar to that of other plant genes and that transcription started at downstream tsp-79bp.
    利用GenomeWalker的方法获得了烟草伤诱导过氧化物酶基因(tpoxN1)的5'调控序列,序列分析表明,烟草的tpoxN1基因的转录起始位点(tspA)的保守序列5'TCAATCA与其它植物基因非常一致,转录从tsp下游79bp处开始。
    MOLECULAR CLONING AND ANALYSIS OF A LIGNIN PEROXIDASE GENE FROM PHANEROCHAETE CHRY SOSPORIUM
    黄孢平革霉(Phanerochaete chrysosporium)木质素过氧化物酶基因的克隆与分析
    To Construct the cDNA Library of Orychophragmus violaceus and Screen the cDNA Sequence of Peroxidase Gene(OvRCI)
    从诸葛菜cDNA文库中筛选过氧化物酶基因
    Cloning and Sequence Analysis of 5'Regulator Region for Wound-Inducible Peroxidase Gene from Tobacco
    烟草伤诱导型过氧化物酶基因(tpoxN1)启动子的克隆及分析
    The Transcript Accumulation of Peroxidase Gene in Rice Suspension-Cultured Cells Treated by Zhongshengmycin
    中生菌素对水稻悬浮细胞过氧化物酶基因转录表达的影响
    THE EFFECT OF POLYSACCHARIDE KRESTIN ON PEROXIDASE GENE EXPRESSION IN MACROPHAGES
    云芝多糖对巨噬细胞谷胱甘肽过氧化物酶基因表达的影响
    New peroxidase gene from Orychophragmus violaceus was cloned. The full-length cDNA of Orychophragmus violaceus peroxidase gene(OvRCI, GenBank Acc. No.bankit 569146) was 1220bp and contained a 1128bp open reading frame encoding a protein of 376 amino acids.
    在200mmol/LNaCl诱导下构建诸葛菜苗期的cDNA文库,并从cDNA文库中筛选到一个新的过氧化物酶基因OvRCI,该基因cDNA全长1220bp,包含了一个1128bp的开放阅读框.
    The 9 of them was applied successfully in the experiment, they are toxin,RNA Cytotoxin Ribonuclease gene, RNA Ribonuclease inhibitor organidation gene, Chitinase gene, β-1,3-Giucanase gene, Ribosome-inactivating protein gene, phytoalexing gene, phytoalexing gene, antibacterial peptide gene, peroxidase gene and pathogenesis-related protein gene.
    在试验研究中应用比较成功的主要有9类,分别是:细胞毒素RNA酶基因、RNA酶抑制剂编码基因、几丁质酶基因、β-1,3-葡聚糖酶基因、核糖体失活蛋白基因、植保素合成酶基因、抗真菌蛋白基因、过氧化物酶基因和病程相关蛋白基因。
    It was found that one of the fragments was similar to the Peroxidase gene located on the rice chromosome 1 completely, another fragment was partially similar to the protein Phosphorylase gene located on the rice chromosome 12 with 99.99% homology.
    对克隆后的差异条带进行了测序和Blast,发现这些差异片段与一些幼穗发育的EST有很高的同源性,同源性均在99%以上。 其中一个与位于水稻第一号染色体的过氧化物酶基因的部分片段有100%相似性,另一个与位于第十二号染色体上的蛋白磷酸化酶基因有99.99%的同源性,分别与两个LTSS基因所在的染色体一致。
    The medium and fermentation method of Pichia methanolica with lignin peroxidase gene(LipH8)of Phanerochaete chrysosporium was investigated. The optimum fermentation method of lignin peroxidase was studied by shake-flask culture. It is good that Pichia methanolica was cultured in the 11°Bx wort medium and then induced in the high temperature malt extract medium.
    对含有黄孢原毛平革菌木质素过氧化物酶基因(LipH8)的甲醇毕赤酵母培养基和发酵方法进行了研究.摇瓶培养条件研究结果表明:用11°Bx麦芽汁培养工程菌,然后用高温浸提液置换诱导产酶较好.5 L发酵罐产酶放大实验结果表明,木质素过氧化物酶较稳定,在72 h木质素过氧化物酶酶活达到最高7 568 U/L.
 

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