...
首页> 外文期刊>Fish & Shellfish Immunology >Molecular cloning and characterization of a cytosolic manganese superoxide dismutase (cytMnSOD) and mitochondrial manganese superoxide dismutase (mtMnSOD) from the kuruma shrimp Marsupenaeus japonicus.
【24h】

Molecular cloning and characterization of a cytosolic manganese superoxide dismutase (cytMnSOD) and mitochondrial manganese superoxide dismutase (mtMnSOD) from the kuruma shrimp Marsupenaeus japonicus.

机译:k虾 Marsupenaeus japonicus 胞质锰超氧化物歧化酶(cytMnSOD)和线粒体锰超氧化物歧化酶(mtMnSOD)的分子克隆和鉴定。

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

A cytosolic manganese superoxide dismutase (cytMnSOD) gene and a mitochondrial manganese superoxide dismutase (mtMnSOD) gene were cloned from the kuruma shrimp Marsupenaeus japonicus using reverse transcription-polymerase chain reaction (RT-PCR) and rapid amplification of cDNA ends (RACE) method. The open reading frame (ORF) of cytMnSOD is 861 bp and encodes a 287 amino acids (aa) protein with a 61 aa leader sequence, whereas the ORF of mtMnSOD is 663 bp and encodes a 221 aa protein with a 21 aa mitochondrial-targeting sequence in the N-terminus. The calculated molecular mass of translated protein of cytMnSOD and mtMnSOD is 31.4 kDa and 24.3 kDa with an estimated pI of 5.62 and 7.27, respectively. The deduced amino acid sequence of cytMnSOD has similarity of 50.2% to that of mtMnSOD. Both cytMnSOD and mtMnSOD contain a manganese superoxide dismutase domain (DVWEHAYY), and four conserved amino acids responsible for binding manganese. Both cytMnSOD and mtMnSOD of M. japonicus were expressed in haemocytes, eyestalk, muscle, intestine, gill, and hepatopancreas. Both cytMnSOD and mtMnSOD transcripts in haemocytes of M. japonicus significantly increased 6 h after injection of Vibrio alginolyticus, and 12 h after injection of beta -glucan, indicating induction of SOD system response in a short time.
机译:利用逆转录-聚合酶链反应(RT-PCR)和快速扩增技术,从黑马虾 Marsupenaeus japonicus 中克隆了胞质锰超氧化物歧化酶(cytMnSOD)基因和线粒体锰超氧化物歧化酶(mtMnSOD)基因。 cDNA末端(RACE)方法。 cytMnSOD的开放阅读框(ORF)为861 bp,编码一个具有61个氨基酸的前导序列的287个氨基酸(aa)蛋白,而mtMnSOD的ORF为663 bp,编码为一个21 aa的线粒体靶向蛋白N末端的序列。 cytMnSOD和mtMnSOD的翻译蛋白的计算分子量为31.4 kDa和24.3 kDa,估计pI I分别为5.62和7.27。推导的cytMnSOD的氨基酸序列与mtMnSOD的相似性为50.2%。 cytMnSOD和mtMnSOD均包含锰超氧化物歧化酶结构域(DVWEHAYY),以及负责结合锰的四个保守氨基酸。 M的cytMnSOD和mtMnSOD两者。刺参在血细胞,眼球,肌肉,肠,muscle和肝胰腺中均有表达。 iM血细胞中的cytMnSOD和mtMnSOD转录本。注射溶藻弧菌6小时后和注射β-葡聚糖后12小时,刺参明显增加,表明在短时间内诱导了SOD系统反应。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号