塑F1FO-ATP合成酶的演变和监管多样化
Kaori Kohzuma1, Sota Muraoka1, Minoru Kumazawa1
1Division of Applied Life Sciences, Graduate School of Agriculture, Kyoto University, Kitashirakawa-Oiwake-cho, Sakyo-ku, Kyoto 606-8502, Japan.
Plant & cell physiology
|August 29, 2025
概括
塑F1FO-ATP合成酶具有独特的氧化还原调节,特别是在具有两个马子单元异型的血管精子中. 这种多样性允许适应光线可用性,并支持非光合作用组织的应力耐受性.
科学领域:
- 生物化学
- 分子生物学
- 进化生物学
背景情况:
- F1FO-ATP合成酶对细胞能量代谢至关重要,可以在细菌,线粒体和塑体中保存.
- 这种酶复合体在结构,同位体和催化机制上表现出显著的调节多样性.
- 塑F1FO-ATP合成酶具有与光可用性相关的氧化还原依赖调节等独特特征.
研究的目的:
- 审查塑F1FO-ATP合成酶的结构,生理和进化方面.
- 探索ATP合成酶的多样化,特别是在塑体中,超出ATP的生产范围.
- 讨论质细胞ATP合成酶中氧化还原调节的必要性.
主要方法:
- 玛 (γ) 子单位的基因分析.
- 整合结构和生理数据.
- 进行比较的进化分析.
主要成果:
- 血管精子具有两种玛子单元异型 (ATPC1和ATPC2),产生氧化还原敏感和不敏感的酶.
- 氧化还原不敏感的形式在黑暗中活跃,有助于调节质子动力.
- 塑ATP合成酶的多样化支持更广泛的生理作用和应激适应.
结论:
- 塑F1FO-ATP合成酶的独特调节多样性是其生理意义的关键.
- 氧化还原调节对于质细胞的ATP合成功能至关重要,适应环境信号.
- ATP合成酶的多样化有助于生物的适应和生存.
相关概念视频
ATP Synthase: Structure
13.0K
ATP synthase or ATPase is among the most conserved proteins found in bacteria, mammals, and plants. This enzyme can catalyze a forward reaction in response to the electrochemical gradient, producing ATP from ADP and inorganic phosphate. ATP synthase can also work in a reverse direction by hydrolyzing ATP and generating an electrochemical gradient. Different forms of ATP synthases have evolved special features to meet the specific demands of the cell. Based on their specific feature, ATP...
13.0K
The Anatomy of Chloroplasts
5.6K
Green algae and plants, including green stems and unripe fruit, harbor specialized organelles called chloroplasts to carry out photosynthesis. They coordinate both stages of photosynthesis — the light-dependent reactions and the light-independent reactions. The light-dependent reactions use sunlight to release oxygen and produce chemical energy in the form of ATP and NADPH, and the light-independent reactions capture CO2 and use ATP and NADPH to produce sugar.
Structure of...
Structure of...
5.6K
Protein Complexes with Interchangeable Parts
2.6K
Groups of proteins may form a complex where each protein in this complex has a different role in the overall execution of the complex’s function. Often some of the proteins in the complex can be replaced by a closely related variant to give a complex that contains many of the same components yet is functionally distinct.
The SCF ubiquitin ligase is a protein complex of five individual proteins. This complex attaches ubiquitin to other target proteins to mark them for degradation. In order...
The SCF ubiquitin ligase is a protein complex of five individual proteins. This complex attaches ubiquitin to other target proteins to mark them for degradation. In order...
2.6K
Protein Transport to the Outer Chloroplast Membrane
2.0K
Chloroplast outer membrane proteins encoded by the nucleus are synthesized in the cytosol. Soon after synthesis, they bind cytosolic factors such as 14-3-3 protein and the Hsp70 chaperones that keep these precursors in an unfolded state until their translocation.
Two models describe the mechanism of precursor recognition and entry across the outer membrane through the TOC complex. Model 1 suggests the newly synthesized precursor binds to the TOC receptor 159 and forms a complex.
Two models describe the mechanism of precursor recognition and entry across the outer membrane through the TOC complex. Model 1 suggests the newly synthesized precursor binds to the TOC receptor 159 and forms a complex.
2.0K
ATP Synthase: Mechanism
15.1K
In animals, the mitochondrial F1F0 ATP synthase is the key protein that synthesizes ATP molecules through a complex catalytic mechanism. While the nuclear genome encodes the majority of ATP synthase subunits, the mitochondrial genome encodes some of the enzyme's most critical components. The formation of this multi-subunit enzyme is a complex multi-step process regulated at the level of transcription, translation, and assembly. Defects in one or more of these steps can result in decreased...
15.1K
Export of Mitochondrial and Chloroplast Genes
3.8K
A eukaryotic cell can have up to three different types of genetic systems: nuclear, mitochondrial, and chloroplast. During evolution, organelles have exported many genes to the nucleus; this transfer is still ongoing in some plant species. Approximately 18% of the Arabidopsis thaliana nuclear genome is thought to be derived from the chloroplast’s cyanobacterial ancestor, and around 75% of the yeast genome derived from the mitochondria’s bacterial ancestor. This export has occurred...
3.8K


