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木瓜蛋白酶编码cDNA的克隆与测序

Cloning and sequencing of papain-encoding cDNA.

作者信息

Cohen L W, Coghlan V M, Dihel L C

出版信息

Gene. 1986;48(2-3):219-27. doi: 10.1016/0378-1119(86)90080-6.

Abstract

Messenger RNA extracted from Carica papaya fruit was converted to cDNA and cloned into the PstI restriction site of plasmid pBR322. Subclones of the approximately 1.4-kb fragment were sequenced. The nucleotide sequence matched that expected, based on the amino acid (aa) sequence for papain, with the following exceptions: at aa positions 47, 118 and 135 the codon for glutamate was found instead of glutamine; at aa position 169 the codon for asparagine was found instead of glycine; at aa positions 86-88, a difference in the order of the aa codons was observed, namely tyr-pro-tyr instead of the published pro-tyr-tyr. The upstream sequence revealed that papain is probably synthesized with a 133-aa prosegment, suggesting that the enzyme is synthesized as an inactive zymogen. The downstream segment revealed an unusual (AT)9AGAA sequence beginning 26 bp from the double TGA stop codon.

摘要

从番木瓜果实中提取的信使核糖核酸(mRNA)被转化为互补脱氧核糖核酸(cDNA),并克隆到质粒pBR322的PstI限制性酶切位点。对大约1.4千碱基(kb)片段的亚克隆进行了测序。根据木瓜蛋白酶的氨基酸(aa)序列,核苷酸序列与之相符,但有以下例外:在氨基酸位置47、118和135处,发现编码谷氨酸的密码子而非谷氨酰胺;在氨基酸位置169处,发现编码天冬酰胺的密码子而非甘氨酸;在氨基酸位置86 - 88处,观察到氨基酸密码子顺序不同,即酪氨酸 - 脯氨酸 - 酪氨酸,而非已发表的脯氨酸 - 酪氨酸 - 酪氨酸。上游序列表明木瓜蛋白酶可能是由一个133个氨基酸的前肽段合成的,这表明该酶是以无活性的酶原形式合成的。下游片段显示了一个不寻常的(AT)9AGAA序列,从双TGA终止密码子开始26个碱基对处。

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