• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

奇特的细胞器——疟原虫线粒体缺乏丙酮酸脱氢酶复合体。

Strange organelles--Plasmodium mitochondria lack a pyruvate dehydrogenase complex.

作者信息

Ralph Stuart A

机构信息

Institut Pasteur, Biology of Host-Parasite Interactions Unit (CNRS URA2581) 25, rue du Docteur Roux, F-75724 PARIS CEDEX 15, France.

出版信息

Mol Microbiol. 2005 Jan;55(1):1-4. doi: 10.1111/j.1365-2958.2004.04314.x.

DOI:10.1111/j.1365-2958.2004.04314.x
PMID:15612911
Abstract

Our understanding of the Plasmodium mitochondrion and apicoplast has been greatly assisted by the genome sequence project. Sequence data have seeded recent research showing that the apicoplast is the site of several anabolic pathways including fatty acid synthesis. The discovery of an active apicoplast pyruvate dehydrogenase complex implies this enzyme generates the acetyl-CoA needed for fatty acid synthesis. However, the absence of a corresponding mitochondrial complex suggests that energy generation in Plasmodium is considerably different from pathways described in other eukaryotes.

摘要

疟原虫线粒体和顶质体的基因组序列项目极大地推动了我们对它们的认识。序列数据为近期的研究提供了基础,这些研究表明顶质体是包括脂肪酸合成在内的多种合成代谢途径的场所。活跃的顶质体丙酮酸脱氢酶复合体的发现意味着该酶产生了脂肪酸合成所需的乙酰辅酶A。然而,相应线粒体复合体的缺失表明疟原虫中的能量产生与其他真核生物中描述的途径有很大不同。

相似文献

1
Strange organelles--Plasmodium mitochondria lack a pyruvate dehydrogenase complex.奇特的细胞器——疟原虫线粒体缺乏丙酮酸脱氢酶复合体。
Mol Microbiol. 2005 Jan;55(1):1-4. doi: 10.1111/j.1365-2958.2004.04314.x.
2
The malaria parasite Plasmodium falciparum has only one pyruvate dehydrogenase complex, which is located in the apicoplast.疟原虫恶性疟原虫只有一种丙酮酸脱氢酶复合体,它位于顶质体中。
Mol Microbiol. 2005 Jan;55(1):39-53. doi: 10.1111/j.1365-2958.2004.04407.x.
3
The human malaria parasite Plasmodium falciparum possesses two distinct dihydrolipoamide dehydrogenases.人类疟原虫恶性疟原虫拥有两种不同的二氢硫辛酰胺脱氢酶。
Mol Microbiol. 2005 Jan;55(1):27-38. doi: 10.1111/j.1365-2958.2004.04398.x.
4
Plasmodium falciparum possesses organelle-specific alpha-keto acid dehydrogenase complexes and lipoylation pathways.恶性疟原虫拥有细胞器特异性的α-酮酸脱氢酶复合物和硫辛酰化途径。
Biochem Soc Trans. 2005 Nov;33(Pt 5):977-80. doi: 10.1042/BST20050977.
5
Diversity in mitochondrial metabolic pathways in parasitic protists Plasmodium and Cryptosporidium.寄生原生生物疟原虫和隐孢子虫线粒体代谢途径的多样性。
Parasitol Int. 2010 Sep;59(3):305-12. doi: 10.1016/j.parint.2010.04.005. Epub 2010 Apr 27.
6
Carbohydrate metabolism in the Toxoplasma gondii apicoplast: localization of three glycolytic isoenzymes, the single pyruvate dehydrogenase complex, and a plastid phosphate translocator.刚地弓形虫质体中的碳水化合物代谢:三种糖酵解同工酶、单一丙酮酸脱氢酶复合体及一种质体磷酸转运体的定位
Eukaryot Cell. 2007 Jun;6(6):984-96. doi: 10.1128/EC.00061-07. Epub 2007 Apr 20.
7
Localisation of gluconeogenesis and tricarboxylic acid (TCA)-cycle enzymes and first functional analysis of the TCA cycle in Toxoplasma gondii.弓形虫中糖异生和三羧酸(TCA)循环酶的定位及TCA循环的首次功能分析
Int J Parasitol. 2008 Aug;38(10):1121-32. doi: 10.1016/j.ijpara.2008.01.007. Epub 2008 Feb 13.
8
c-Jun N-terminal kinase regulates mitochondrial bioenergetics by modulating pyruvate dehydrogenase activity in primary cortical neurons.c-Jun氨基末端激酶通过调节原代皮质神经元中的丙酮酸脱氢酶活性来调控线粒体生物能量学。
J Neurochem. 2008 Jan;104(2):325-35. doi: 10.1111/j.1471-4159.2007.04957.x. Epub 2007 Oct 18.
9
[Mitochondrial Pyruvate dehydrogenase].[线粒体丙酮酸脱氢酶]
Nihon Rinsho. 2002 Apr;60 Suppl 4:118-21.
10
Pyruvate kinase type-II isozyme in Plasmodium falciparum localizes to the apicoplast.恶性疟原虫中的丙酮酸激酶II型同工酶定位于顶质体。
Parasitol Int. 2009 Mar;58(1):101-5. doi: 10.1016/j.parint.2008.10.005. Epub 2008 Oct 31.

引用本文的文献

1
Characterisation of the Piroplasm Proteome across Three Common Genotypes.三种常见基因型梨形虫蛋白质组的表征
Pathogens. 2022 Sep 30;11(10):1135. doi: 10.3390/pathogens11101135.
2
Macromeront Formation Induces Glycolytic Responses and Mitochondrial Changes in Primary Host Endothelial Cells.巨细胞形成诱导原代宿主内皮细胞的糖酵解反应和线粒体变化。
Front Cell Infect Microbiol. 2021 Jul 15;11:703413. doi: 10.3389/fcimb.2021.703413. eCollection 2021.
3
Annotation and characterization of Babesia gibsoni apicoplast genome.巴贝斯虫属 gibsoni 顶复体基因组的注释和特征描述。
Parasit Vectors. 2020 Apr 21;13(1):209. doi: 10.1186/s13071-020-04065-7.
4
Proteomic analysis revealed alterations of the metabolism following salicylhydroxamic acid exposure.蛋白质组学分析揭示了水杨羟肟酸暴露后代谢的变化。
Res Rep Trop Med. 2011 Sep 8;2:109-119. doi: 10.2147/RRTM.S23127. eCollection 2011.
5
Comparative sequence analysis of Cyclospora cayetanensis apicoplast genomes originating from diverse geographical regions.来自不同地理区域的卡耶塔环孢子虫顶质体基因组的比较序列分析。
Parasit Vectors. 2016 Nov 29;9(1):611. doi: 10.1186/s13071-016-1896-4.
6
BCKDH: the missing link in apicomplexan mitochondrial metabolism is required for full virulence of Toxoplasma gondii and Plasmodium berghei.支链α-酮酸脱氢酶:顶复门原虫线粒体代谢中缺失的环节是刚地弓形虫和伯氏疟原虫完全毒力所必需的。
PLoS Pathog. 2014 Jul 17;10(7):e1004263. doi: 10.1371/journal.ppat.1004263. eCollection 2014 Jul.
7
Protein S-nitrosylation in Plasmodium falciparum.恶性疟原虫中的蛋白质S-亚硝基化
Antioxid Redox Signal. 2014 Jun 20;20(18):2923-35. doi: 10.1089/ars.2013.5553. Epub 2014 Feb 4.
8
Kinetic flux profiling elucidates two independent acetyl-CoA biosynthetic pathways in Plasmodium falciparum.动力学通量分析揭示恶性疟原虫中有两条独立的乙酰辅酶 A 生物合成途径。
J Biol Chem. 2013 Dec 20;288(51):36338-50. doi: 10.1074/jbc.M113.503557. Epub 2013 Oct 25.
9
The 2-methylcitrate cycle is implicated in the detoxification of propionate in Toxoplasma gondii.2-甲基柠檬酸循环参与弓形虫中丙酸盐的解毒。
Mol Microbiol. 2013 Feb;87(4):894-908. doi: 10.1111/mmi.12139. Epub 2013 Jan 11.
10
Host cell egress and invasion induce marked relocations of glycolytic enzymes in Toxoplasma gondii tachyzoites.宿主细胞逸出和入侵会引起刚地弓形虫速殖子中糖酵解酶的显著重新定位。
PLoS Pathog. 2008 Oct;4(10):e1000188. doi: 10.1371/journal.ppat.1000188. Epub 2008 Oct 24.