Suppr超能文献

黄素还原酶:来自牛肝脏的cDNA序列及组织分布

Flavin reductase: sequence of cDNA from bovine liver and tissue distribution.

作者信息

Quandt K S, Hultquist D E

机构信息

Department of Biological Chemistry, University of Michigan, Ann Arbor 48109-0606.

出版信息

Proc Natl Acad Sci U S A. 1994 Sep 27;91(20):9322-6. doi: 10.1073/pnas.91.20.9322.

Abstract

Flavin reductase catalyzes electron transfer from reduced pyridine nucleotides to methylene blue or riboflavin, and this catalysis is the basis of the therapeutic use of methylene blue or riboflavin in the treatment of methemoglobinemia. A cDNA for a mammalian flavin reductase has been isolated and sequenced. Degenerate oligonucleotides, with sequences based on amino acid sequences of peptides derived from bovine erythrocyte flavin reductase, were used as primers in PCR to selectively amplify a partial cDNA that encodes the bovine reductase. The template used in the PCR was first strand cDNA synthesized from bovine liver total RNA using oligo(dT) primers. A PCR product was used as a specific probe to screen a bovine liver cDNA library. The sequence determined from two overlapping clones contains an open reading frame of 621 nucleotides and encodes 206 amino acids. The amino acid sequence deduced from the bovine liver flavin reductase cDNA matches the amino acid sequences determined for erythrocyte reductase-derived peptides, and the predicted molecular mass of 22,001 Da for the liver reductase agrees well with the molecular mass of 21,994 Da determined for the erythrocyte reductase by electrospray mass spectrometry. The amino acid sequence at the N terminus of the reductase has homology to sequences of pyridine nucleotide-dependent enzymes, and the predicted secondary structure, beta alpha beta, resembles the common nucleotide-binding structural motif. RNA blot analysis indicates a single 1-kilobase reductase transcript in human heart, kidney, liver, lung, pancreas, placenta, and skeletal muscle.

摘要

黄素还原酶催化电子从还原型吡啶核苷酸转移至亚甲蓝或核黄素,这种催化作用是亚甲蓝或核黄素用于治疗高铁血红蛋白血症的治疗基础。一种哺乳动物黄素还原酶的cDNA已被分离并测序。以来源于牛红细胞黄素还原酶的肽段氨基酸序列为基础设计的简并寡核苷酸用作PCR引物,以选择性扩增编码牛还原酶的部分cDNA。PCR中使用的模板是用寡聚(dT)引物从牛肝总RNA合成的第一链cDNA。PCR产物用作特异性探针筛选牛肝cDNA文库。从两个重叠克隆确定的序列包含一个621个核苷酸的开放阅读框,编码206个氨基酸。从牛肝黄素还原酶cDNA推导的氨基酸序列与针对红细胞还原酶衍生肽段确定的氨基酸序列匹配,肝脏还原酶预测的分子量为22,001 Da,与通过电喷雾质谱法确定的红细胞还原酶21,994 Da的分子量非常吻合。还原酶N端的氨基酸序列与吡啶核苷酸依赖性酶的序列具有同源性,预测的二级结构β-α-β类似于常见的核苷酸结合结构基序。RNA印迹分析表明在人心脏、肾脏、肝脏、肺、胰腺、胎盘和骨骼肌中有一个1千碱基的还原酶转录本。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/05d2/44804/085eadd7033d/pnas01142-0136-a.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验