{"title":"Isolation and Measurement of Respiration and Structural Studies of Purified Mitochondria from Heterotrophic Plant Tissues.","authors":"Sonika Pandey, Aprajita Kumari, Pooja Singh, Kapuganti Jagadis Gupta","doi":"10.1002/cpz1.326","DOIUrl":null,"url":null,"abstract":"<p><p>Mitochondria are the power houses of eukaryotic cells. These organelles contain various oxidoreductase complexes. Electron transfer from different reducing equivalents channeled via these complexes drives proton translocation across the inner mitochondrial membrane, leading to ATP generation. Plant mitochondria contain alternative NAD(P)H dehydrogenases, alternative oxidase, and uncoupling protein, and TCA cycle enzymes are located in their matrix. Apart from ATP production, mitochondria are also involved in synthesis of vitamins and cofactors and participate in fatty acid, nucleotide, photorespiratory, and antioxidant metabolism. Recent emerging evidence suggests that mitochondria play a role in redox signaling and generation of reactive oxygen and nitrogen species. For mitochondrial studies, it is essential to isolate physiologically active mitochondria with good structural integrity. In this article, we explain a detailed procedure for isolation of mitochondria from various heterotrophic tissues, such as germinating chickpea seeds, potato tubers, and cauliflower florets. This procedure requires discontinuous Percoll gradient centrifugation and can give a good yield of mitochondria, in the range of 4 to 8 mg per 50 g tissue with active respiratory capacity. After MitoTracker staining, isolated mitochondria can be visualized by using a confocal microscope. The structure of mitochondria can be monitored by scanning electron microscopy. © 2021 Wiley Periodicals LLC. Basic Protocol 1: Isolation of mitochondria from germinating chickpea seeds, potato tubers, and cauliflower florets Basic Protocol 2: Quantification of mitochondrial protein concentration by Bradford assay Basic Protocol 3: Quantification of mitochondrial respiration using single-channel free-radical analyzer Basic Protocol 4: Staining of mitochondria and confocal imaging Basic Protocol 5: Visualization of isolated mitochondria under scanning electron microscope.</p>","PeriodicalId":11174,"journal":{"name":"Current Protocols","volume":" ","pages":"e326"},"PeriodicalIF":0.0000,"publicationDate":"2021-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current Protocols","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1002/cpz1.326","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Mitochondria are the power houses of eukaryotic cells. These organelles contain various oxidoreductase complexes. Electron transfer from different reducing equivalents channeled via these complexes drives proton translocation across the inner mitochondrial membrane, leading to ATP generation. Plant mitochondria contain alternative NAD(P)H dehydrogenases, alternative oxidase, and uncoupling protein, and TCA cycle enzymes are located in their matrix. Apart from ATP production, mitochondria are also involved in synthesis of vitamins and cofactors and participate in fatty acid, nucleotide, photorespiratory, and antioxidant metabolism. Recent emerging evidence suggests that mitochondria play a role in redox signaling and generation of reactive oxygen and nitrogen species. For mitochondrial studies, it is essential to isolate physiologically active mitochondria with good structural integrity. In this article, we explain a detailed procedure for isolation of mitochondria from various heterotrophic tissues, such as germinating chickpea seeds, potato tubers, and cauliflower florets. This procedure requires discontinuous Percoll gradient centrifugation and can give a good yield of mitochondria, in the range of 4 to 8 mg per 50 g tissue with active respiratory capacity. After MitoTracker staining, isolated mitochondria can be visualized by using a confocal microscope. The structure of mitochondria can be monitored by scanning electron microscopy. © 2021 Wiley Periodicals LLC. Basic Protocol 1: Isolation of mitochondria from germinating chickpea seeds, potato tubers, and cauliflower florets Basic Protocol 2: Quantification of mitochondrial protein concentration by Bradford assay Basic Protocol 3: Quantification of mitochondrial respiration using single-channel free-radical analyzer Basic Protocol 4: Staining of mitochondria and confocal imaging Basic Protocol 5: Visualization of isolated mitochondria under scanning electron microscope.
异养植物组织中纯化线粒体的分离、呼吸作用测定及结构研究。
线粒体是真核细胞的能量发电站。这些细胞器含有各种氧化还原酶复合物。来自不同还原等价物的电子转移通过这些复合物驱动质子在线粒体内膜上的易位,导致ATP的产生。植物线粒体含有替代NAD(P)H脱氢酶、替代氧化酶和解偶联蛋白,TCA循环酶位于其基质中。除了ATP的产生外,线粒体还参与维生素和辅助因子的合成,并参与脂肪酸、核苷酸、光呼吸和抗氧化代谢。最近出现的证据表明,线粒体在氧化还原信号和活性氧和活性氮的产生中发挥作用。对于线粒体的研究,分离具有良好结构完整性的生理活性线粒体是必不可少的。在这篇文章中,我们详细解释了从各种异养组织中分离线粒体的过程,如发芽的鹰嘴豆种子、马铃薯块茎和花椰菜小花。该程序需要不连续的Percoll梯度离心,并且可以提供良好的线粒体产量,在每50克组织4至8毫克的范围内,呼吸能力活跃。在MitoTracker染色后,可以用共聚焦显微镜观察分离的线粒体。线粒体的结构可以用扫描电子显微镜观察。©2021 Wiley期刊有限责任公司。基本方案1:从发芽的嘴豆种子、马铃薯块茎和花椰菜小花中分离线粒体。基本方案2:用Bradford法定量线粒体蛋白浓度。基本方案3:用单通道自由基分析仪定量线粒体呼吸。基本方案4:线粒体染色和共聚焦成像。基本方案5:在扫描电镜下观察分离的线粒体。
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