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鉴定酿酒酵母第八条染色体上的YHR068w为脱氧hypusine合酶基因。该酶的表达与特性研究。

Identification of YHR068w in Saccharomyces cerevisiae chromosome VIII as a gene for deoxyhypusine synthase. Expression and characterization of the enzyme.

作者信息

Kang K R, Wolff E C, Park M H, Folk J E, Chung S I

机构信息

Enzyme Chemistry Section, NIDR, National Institutes of Health, Bethesda, Maryland 20892-4330, USA.

出版信息

J Biol Chem. 1995 Aug 4;270(31):18408-12. doi: 10.1074/jbc.270.31.18408.

Abstract

Deoxyhypusine synthase catalyzes the formation of deoxyhypusine, the first step in hypusine biosynthesis. Amino acid sequences of five tryptic peptides from rat deoxyhypusine synthase were found to match partially the deduced amino acid sequence of the open reading frame of gene YHR068w of Saccharomyces cerevisiae chromosome VIII (AC:U00061). In order to determine whether the product of this gene corresponds to yeast deoxyhypusine synthase,a 1.17-kilobase pair cDNA with an identical nucleotide sequence to that of the YHR068w coding region was obtained from S. cerevisiae cDNA by polymerase chain reaction and was expressed in Escherichia coli B strain BL21 (DE3). The recombinant protein was found mostly in the E. coli cytosol fraction and comprised approximately 20% of the total soluble protein. The purified form of the expressed protein effectively catalyzed the formation of deoxyhypusine in yeast eIF-5A precursors as well as in human precursor and in those from Chinese hamster ovary cells. The molecular mass of the enzyme was estimated to be 172,000 +/- 4,300 Da by equilibrium centrifugation. The mass of its polypeptide subunit was determined to be approximately 43,000 Da, in close agreement with that calculated for the coding region of the YHRO68w gene. These findings show that this gene is a coding sequence for yeast deoxyhypusine synthase and that the product of this gene exists in a tetrameric form.

摘要

脱氧hypusine合酶催化脱氧hypusine的形成,这是hypusine生物合成的第一步。发现来自大鼠脱氧hypusine合酶的五个胰蛋白酶肽的氨基酸序列与酿酒酵母VIII号染色体基因YHR068w(AC:U00061)开放阅读框推导的氨基酸序列部分匹配。为了确定该基因的产物是否对应于酵母脱氧hypusine合酶,通过聚合酶链反应从酿酒酵母cDNA中获得了一个1.17千碱基对的cDNA,其核苷酸序列与YHR068w编码区的相同,并在大肠杆菌B株BL21(DE3)中表达。重组蛋白主要存在于大肠杆菌胞质溶胶部分,约占总可溶性蛋白的20%。纯化形式的表达蛋白能有效催化酵母eIF-5A前体、人源前体以及中国仓鼠卵巢细胞来源的前体中脱氧hypusine的形成。通过平衡离心法估计该酶的分子量为172,000 +/- 4,300 Da。其多肽亚基的质量确定约为43,000 Da,与根据YHRO68w基因编码区计算的结果非常一致。这些发现表明该基因是酵母脱氧hypusine合酶的编码序列,且该基因的产物以四聚体形式存在。

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