Advances in photosynthesis research: Unlocking the potential for food security, renewable energy, and environmental sustainability

IF 9.3 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Wenqiang Yang, Rongcheng Lin
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Improving photosynthetic efficiency can directly increase crop yields, helping to address the pressure of global population growth on food demand. Photosynthesis is also a core component of the Earth's carbon cycle, helping to maintain the balance of carbon dioxide and oxygen in the atmosphere and mitigating the effects of the greenhouse effect. Research on photosynthesis has also inspired the development of renewable energy. By mimicking the mechanisms of photosynthesis to design artificial photosynthetic systems, solar energy can be converted into clean energy for human beings. Focusing on photosynthesis research can help solve human challenges related to food, energy, and the environment. In recent years, extensive research has been conducted on the essence of energy absorption, transfer, and conversion in photosynthesis, yielding fruitful results. This special issue on photosynthesis research includes 10 articles, comprising three reviews, five research papers, and two commentaries.</p><p>Chloroplasts are the sites where photosynthesis occurs, and chloroplast biogenesis is a prerequisite for the smooth progression of photosynthesis. <span>Frangedakis et al. (2024)</span> explored the novel roles of MpRR-MYB2 and MpRR-MYB5 in chloroplast biogenesis, revealing their interactions with GOLDEN-LIKE (GLK) and GATA transcription factors. <span>Kushwaha et al. (2025)</span> commented on this research, noting that these MYB transcription factors not only regulate chloroplast development but also influence the expression of genes related to photosynthesis, photorespiration, and carbon fixation. Although MYB and GLK have synergistic roles in chloroplast biogenesis, MYB cannot fully replace GLK's functions. The commentary also pointed out that MYB transcription factors play a significant role in the development of male reproductive organs in plants. Future research should further explore the epigenetic regulation of MYB genes and their roles in stress responses, providing new insight for improving crop photosynthetic efficiency and yield. As semi-autonomous organelles, nearly 3,000 proteins in chloroplasts are transported from the cytoplasm. In this special issue, <span>Xing et al. (2025)</span> reviewed the latest advances in chloroplast protein import complexes (the outer chloroplast (TOC)–the inner chloroplast (TIC)) and their regulatory mechanisms. They detailed the structure and function of TOC and TIC complexes and their roles in chloroplast protein import, particularly new models revealed through cryo-electron microscopy. Although the composition of the TOC complex is relatively conserved, the composition of the TIC complex and its associated motor proteins remains controversial, with some components (such as Tic110 and Tic40) from traditional models not supported by recent studies. The article also discussed the quality control and retrograde signaling mechanisms of chloroplast protein import, emphasizing the important role of the ubiquitin-proteasome system in regulating protein import. Additionally, future research directions were proposed, including exploring the structural and functional differences of TOC–TIC complexes in different species and the impact of protein folding states on import pathways. This review provides critical insight into the molecular mechanisms of chloroplast protein import and lays the foundation for further research in related fields. Chlorophyll plays a crucial role in photoelectric conversion. <span>Li et al. (2025)</span> comprehensively reviewed the regulation of chlorophyll biosynthesis pathways and retrograde signaling networks, highlighting chlorophyll's central role in photosynthesis and its importance in plant development and environmental responses. They detailed the enzymatic regulation, transcriptional and post-translational modifications of chlorophyll synthesis, as well as the retrograde signaling mechanisms between chloroplasts and the nucleus. By integrating the latest research findings, they demonstrated the complexity and diversity of chlorophyll metabolism and pointed out its potential applications in synthetic biology and agriculture. This review provides in-depth insight into the regulatory mechanisms of chlorophyll biosynthesis and lays a solid foundation for future research and applications.</p><p>The key first step in achieving efficient energy absorption, transfer, and conversion in photosynthesis is the light-harvesting process. In recent years, significant progress has been made in understanding the light-harvesting complexes of photosynthetic organisms through structural biology. <span>Huang et al. (2025)</span> reported the structure of the smallest reaction center–light-harvesting complex (CaRC–LH) in the photosynthetic bacterium <i>Chloroflexus aurantiacus</i>, resolved using cryo-electron microscopy at a resolution of 3.05 Å. This complex consists of only seven light-harvesting subunits, forming a crescent shape around the mobile quinone-binding site of the reaction center. The study revealed the detailed organization and cofactor arrangement of this minimal light-harvesting complex, explaining why this bacterium requires an additional light-harvesting antenna—the chlorosome—to ensure sufficient light capture. The article also explored the electron transfer pathways and the binding mechanisms between the complex and the chlorosome, providing new insight into the diversity of light capture and energy transfer in photosynthesis. This discovery not only sheds light on the evolutionary adaptability of photosynthetic bacteria, but also offers important references for research on photosynthetic mechanisms.</p><p>Photosynthetic carbon fixation is a critical step in converting unstable chemical energy into stable chemical energy. In addition to the C<sub>3</sub>, C<sub>4</sub>, and CAM carbon fixation types, there are diverse carbon fixation mechanisms in nature. Recently, <span>Liu et al. (2024)</span> published the genome of <i>Eleocharis vivipara</i>, revealing the unique mechanism by which this amphibious plant uses C<sub>3</sub> and C<sub>4</sub> photosynthesis for carbon fixation underwater and on land, respectively. <span>Besnard (2025)</span> commented on this achievement, noting that this photosynthetic plasticity might have been acquired through hybridization or polyploidization events, with genomic recombination and epigenetic regulation playing key roles in its C<sub>3</sub>–C<sub>4</sub> transition. Although the study provided important genomic and transcriptomic resources, some questions remain unresolved, such as the origin and evolutionary history of C<sub>4</sub> photosynthesis genes. Future phylogenomic studies are expected to further elucidate these mechanisms and offer potential applications for crop improvement. Ribulose-1,5-bisphosphate carboxylase/oxygenase (RuBisCO) is the most abundant enzyme on Earth and directly determines the efficiency of photosynthesis. However, as a key enzyme in photosynthesis, its inefficiency and sensitivity to oxygen limit plant carbon fixation efficiency. <span>Qin et al. (2025)</span> comprehensively discussed the progress and challenges in plant carbon assimilation engineering, particularly focusing on optimizing RuBisCO and developing novel carbon fixation pathways. The authors detailed strategies such as directed evolution, rational design, chimeric enzymes, and cofactor engineering to improve RuBisCO's catalytic efficiency. Additionally, the article discussed the use of microcompartments (such as carboxysomes and bundle-sheath cells in C<sub>4</sub> plants) to increase CO<sub>2</sub> concentration and reduce photorespiratory losses. Although some success has been achieved in laboratory and model organisms, implementing these engineered pathways in higher plants has remained challenging. This review demonstrates that, through synthetic biology and artificial intelligence, it is possible to significantly improve crop yields and photosynthetic efficiency in the future, offering solutions to global climate change and food security. The oxygenase activity of RuBisCO also limits its efficient carbon fixation. <span>Mo et al. (2025)</span> successfully improved photosynthetic carbon fixation efficiency and panicle structure in rice by engineering a photorespiration-dependent glycine betaine (GB) biosynthesis pathway. The research team introduced a glycine methylation pathway (imGS) from halophilic cyanobacteria into rice mitochondria, converting glycine produced during photorespiration into GB while reducing the levels of photorespiratory intermediates, thereby decreasing carbon loss from photorespiration and increasing photosynthetic rates and carbohydrate accumulation. Additionally, imGS rice showed improved panicle structure, with significantly increased branch and grain numbers, although the seed-setting rate and thousand-grain weight decreased. This study provides a new strategy for enhancing crop photosynthetic efficiency and yield through mitochondrial photorespiration bypass, with significant application potential.</p><p>Photosynthetic organisms employ various strategies to cope with environmental stresses to ensure the smooth progression of photosynthesis. In this special issue, <span>Feng et al. (2025)</span> used cryo-electron microscopy to resolve the structure of the PSI–FCPI (photosystem I–fucoxanthin chlorophyll <i>a</i>/<i>c</i>-binding protein Is) supercomplex in <i>Thalassiosira pseudonana</i> (Tp) under high-light conditions, revealing the light adaptation strategies of diatoms in high-light environments. They found that Tp–PSI–FCPI reduced the number of peripheral FCPI under high light to avoid photodamage, while retaining five stable FCPI subunits rich in diadinoxanthin (Ddx)/diatoxanthin (Dtx), which may be involved in energy dissipation. The article also proposed the assembly mechanism of PSI–FCPI, emphasizing the key roles of Tp-FCP3 and Tp-Lhcr3 in stabilizing FCPI binding. These findings provide new insight into how diatoms adapt to fluctuating light intensities in marine environments and reveal the unique evolutionary strategies of diatom photosynthetic systems. <span>Ali et al. (2025)</span> studied the antagonistic regulatory mechanisms of VvHY5 and VvBEE1 on resveratrol (Res) biosynthesis in grapevine (<i>Vitis vinifera</i> L.) under high light stress. The study found that high-light-induced VvHY5 activated the expression of stilbene synthase genes (<i>VvSTS</i>), promoting Res accumulation and alleviating photoinhibition and oxidative damage. In contrast, VvBEE1 inhibited Res synthesis by competing with VvHY5 for binding to the <i>VvSTS</i> promoter, exacerbating photodamage. The research also revealed the interaction between light signaling and brassinosteroid (BR) signaling under high light stress, indicating that the antagonistic roles of VvHY5 and VvBEE1 play a key role in regulating grapevine photoprotection mechanisms. These findings provide new insight into how plants cope with high light stress and offer potential strategies for improving crop stress tolerance. <span>Cao et al. (2025)</span> studied the regulatory mechanism of the FaNAC047–FaNAC058 module in heat stress-induced leaf senescence in tall fescue (<i>Festuca arundinacea</i>). The study found that FaNAC047 directly activated chlorophyll degradation genes (<i>FaNYC1</i>, <i>FaNOL</i>, <i>FaSGR</i>) and inhibited catalase gene (<i>FaCAT2</i>) expression, promoting chlorophyll degradation and reactive oxygen species (ROS) accumulation, thereby accelerating heat-induced leaf senescence. Additionally, FaNAC047 forms a protein complex with FaNAC058, further enhancing the regulation of downstream genes. This study reveals the critical role of the FaNAC047–FaNAC058 module in heat stress-induced leaf senescence and provides new genetic resources for breeding heat-tolerant plants.</p><p>Photosynthesis research will continue to make breakthroughs in multiple fields, driving advancements in agriculture, ecology, and renewable energy. First, with the progress of synthetic biology and gene-editing technologies, researchers can more precisely engineer photosynthetic pathways to optimize light energy utilization efficiency and carbon fixation capacity. For example, by introducing artificial photorespiration bypasses or enhancing RuBisCO activity, it is possible to significantly improve crop photosynthetic efficiency and yield, addressing global food security challenges. Second, photosynthesis research will help to understand how plants respond to environmental stresses such as high temperatures, drought, and salinity. By uncovering the photosynthetic regulatory mechanisms under various stresses, more stress-resistant crop varieties can be developed, enhancing agricultural sustainability. Additionally, photosynthesis research will provide new ideas for renewable energy development. Artificial photosynthetic systems aim to mimic natural photosynthesis, efficiently converting solar energy into hydrogen or other clean fuels. Such technologies have the potential to become important alternatives to fossil fuels, reducing greenhouse gas emissions and mitigating climate change. Finally, fundamental research on photosynthesis will deepen our understanding of the origin and evolution of life. By comparing photosynthetic mechanisms across different organisms, the evolutionary history of photosynthesis and its critical role in life evolution can be revealed. In summary, photosynthesis research has broad application prospects in agriculture, ecology, and energy, providing essential support for the sustainable development of human society.</p>","PeriodicalId":195,"journal":{"name":"Journal of Integrative Plant Biology","volume":"67 4","pages":"879-881"},"PeriodicalIF":9.3000,"publicationDate":"2025-04-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1111/jipb.13908","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Integrative Plant Biology","FirstCategoryId":"99","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1111/jipb.13908","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Photosynthesis is the most important biochemical process and the largest-scale process of matter and energy conversion on Earth. It is the process by which plants, algae, and certain bacteria convert light energy into chemical energy. Through photosynthesis, solar energy is used to transform carbon dioxide and water into organic matter (such as glucose) and oxygen. This process not only provides energy and growth materials for plants themselves, but also supplies food and oxygen for other organisms in the ecosystems. The organic matter accumulated by crops through photosynthesis is the primary source of food for humans and animals. Improving photosynthetic efficiency can directly increase crop yields, helping to address the pressure of global population growth on food demand. Photosynthesis is also a core component of the Earth's carbon cycle, helping to maintain the balance of carbon dioxide and oxygen in the atmosphere and mitigating the effects of the greenhouse effect. Research on photosynthesis has also inspired the development of renewable energy. By mimicking the mechanisms of photosynthesis to design artificial photosynthetic systems, solar energy can be converted into clean energy for human beings. Focusing on photosynthesis research can help solve human challenges related to food, energy, and the environment. In recent years, extensive research has been conducted on the essence of energy absorption, transfer, and conversion in photosynthesis, yielding fruitful results. This special issue on photosynthesis research includes 10 articles, comprising three reviews, five research papers, and two commentaries.

Chloroplasts are the sites where photosynthesis occurs, and chloroplast biogenesis is a prerequisite for the smooth progression of photosynthesis. Frangedakis et al. (2024) explored the novel roles of MpRR-MYB2 and MpRR-MYB5 in chloroplast biogenesis, revealing their interactions with GOLDEN-LIKE (GLK) and GATA transcription factors. Kushwaha et al. (2025) commented on this research, noting that these MYB transcription factors not only regulate chloroplast development but also influence the expression of genes related to photosynthesis, photorespiration, and carbon fixation. Although MYB and GLK have synergistic roles in chloroplast biogenesis, MYB cannot fully replace GLK's functions. The commentary also pointed out that MYB transcription factors play a significant role in the development of male reproductive organs in plants. Future research should further explore the epigenetic regulation of MYB genes and their roles in stress responses, providing new insight for improving crop photosynthetic efficiency and yield. As semi-autonomous organelles, nearly 3,000 proteins in chloroplasts are transported from the cytoplasm. In this special issue, Xing et al. (2025) reviewed the latest advances in chloroplast protein import complexes (the outer chloroplast (TOC)–the inner chloroplast (TIC)) and their regulatory mechanisms. They detailed the structure and function of TOC and TIC complexes and their roles in chloroplast protein import, particularly new models revealed through cryo-electron microscopy. Although the composition of the TOC complex is relatively conserved, the composition of the TIC complex and its associated motor proteins remains controversial, with some components (such as Tic110 and Tic40) from traditional models not supported by recent studies. The article also discussed the quality control and retrograde signaling mechanisms of chloroplast protein import, emphasizing the important role of the ubiquitin-proteasome system in regulating protein import. Additionally, future research directions were proposed, including exploring the structural and functional differences of TOC–TIC complexes in different species and the impact of protein folding states on import pathways. This review provides critical insight into the molecular mechanisms of chloroplast protein import and lays the foundation for further research in related fields. Chlorophyll plays a crucial role in photoelectric conversion. Li et al. (2025) comprehensively reviewed the regulation of chlorophyll biosynthesis pathways and retrograde signaling networks, highlighting chlorophyll's central role in photosynthesis and its importance in plant development and environmental responses. They detailed the enzymatic regulation, transcriptional and post-translational modifications of chlorophyll synthesis, as well as the retrograde signaling mechanisms between chloroplasts and the nucleus. By integrating the latest research findings, they demonstrated the complexity and diversity of chlorophyll metabolism and pointed out its potential applications in synthetic biology and agriculture. This review provides in-depth insight into the regulatory mechanisms of chlorophyll biosynthesis and lays a solid foundation for future research and applications.

The key first step in achieving efficient energy absorption, transfer, and conversion in photosynthesis is the light-harvesting process. In recent years, significant progress has been made in understanding the light-harvesting complexes of photosynthetic organisms through structural biology. Huang et al. (2025) reported the structure of the smallest reaction center–light-harvesting complex (CaRC–LH) in the photosynthetic bacterium Chloroflexus aurantiacus, resolved using cryo-electron microscopy at a resolution of 3.05 Å. This complex consists of only seven light-harvesting subunits, forming a crescent shape around the mobile quinone-binding site of the reaction center. The study revealed the detailed organization and cofactor arrangement of this minimal light-harvesting complex, explaining why this bacterium requires an additional light-harvesting antenna—the chlorosome—to ensure sufficient light capture. The article also explored the electron transfer pathways and the binding mechanisms between the complex and the chlorosome, providing new insight into the diversity of light capture and energy transfer in photosynthesis. This discovery not only sheds light on the evolutionary adaptability of photosynthetic bacteria, but also offers important references for research on photosynthetic mechanisms.

Photosynthetic carbon fixation is a critical step in converting unstable chemical energy into stable chemical energy. In addition to the C3, C4, and CAM carbon fixation types, there are diverse carbon fixation mechanisms in nature. Recently, Liu et al. (2024) published the genome of Eleocharis vivipara, revealing the unique mechanism by which this amphibious plant uses C3 and C4 photosynthesis for carbon fixation underwater and on land, respectively. Besnard (2025) commented on this achievement, noting that this photosynthetic plasticity might have been acquired through hybridization or polyploidization events, with genomic recombination and epigenetic regulation playing key roles in its C3–C4 transition. Although the study provided important genomic and transcriptomic resources, some questions remain unresolved, such as the origin and evolutionary history of C4 photosynthesis genes. Future phylogenomic studies are expected to further elucidate these mechanisms and offer potential applications for crop improvement. Ribulose-1,5-bisphosphate carboxylase/oxygenase (RuBisCO) is the most abundant enzyme on Earth and directly determines the efficiency of photosynthesis. However, as a key enzyme in photosynthesis, its inefficiency and sensitivity to oxygen limit plant carbon fixation efficiency. Qin et al. (2025) comprehensively discussed the progress and challenges in plant carbon assimilation engineering, particularly focusing on optimizing RuBisCO and developing novel carbon fixation pathways. The authors detailed strategies such as directed evolution, rational design, chimeric enzymes, and cofactor engineering to improve RuBisCO's catalytic efficiency. Additionally, the article discussed the use of microcompartments (such as carboxysomes and bundle-sheath cells in C4 plants) to increase CO2 concentration and reduce photorespiratory losses. Although some success has been achieved in laboratory and model organisms, implementing these engineered pathways in higher plants has remained challenging. This review demonstrates that, through synthetic biology and artificial intelligence, it is possible to significantly improve crop yields and photosynthetic efficiency in the future, offering solutions to global climate change and food security. The oxygenase activity of RuBisCO also limits its efficient carbon fixation. Mo et al. (2025) successfully improved photosynthetic carbon fixation efficiency and panicle structure in rice by engineering a photorespiration-dependent glycine betaine (GB) biosynthesis pathway. The research team introduced a glycine methylation pathway (imGS) from halophilic cyanobacteria into rice mitochondria, converting glycine produced during photorespiration into GB while reducing the levels of photorespiratory intermediates, thereby decreasing carbon loss from photorespiration and increasing photosynthetic rates and carbohydrate accumulation. Additionally, imGS rice showed improved panicle structure, with significantly increased branch and grain numbers, although the seed-setting rate and thousand-grain weight decreased. This study provides a new strategy for enhancing crop photosynthetic efficiency and yield through mitochondrial photorespiration bypass, with significant application potential.

Photosynthetic organisms employ various strategies to cope with environmental stresses to ensure the smooth progression of photosynthesis. In this special issue, Feng et al. (2025) used cryo-electron microscopy to resolve the structure of the PSI–FCPI (photosystem I–fucoxanthin chlorophyll a/c-binding protein Is) supercomplex in Thalassiosira pseudonana (Tp) under high-light conditions, revealing the light adaptation strategies of diatoms in high-light environments. They found that Tp–PSI–FCPI reduced the number of peripheral FCPI under high light to avoid photodamage, while retaining five stable FCPI subunits rich in diadinoxanthin (Ddx)/diatoxanthin (Dtx), which may be involved in energy dissipation. The article also proposed the assembly mechanism of PSI–FCPI, emphasizing the key roles of Tp-FCP3 and Tp-Lhcr3 in stabilizing FCPI binding. These findings provide new insight into how diatoms adapt to fluctuating light intensities in marine environments and reveal the unique evolutionary strategies of diatom photosynthetic systems. Ali et al. (2025) studied the antagonistic regulatory mechanisms of VvHY5 and VvBEE1 on resveratrol (Res) biosynthesis in grapevine (Vitis vinifera L.) under high light stress. The study found that high-light-induced VvHY5 activated the expression of stilbene synthase genes (VvSTS), promoting Res accumulation and alleviating photoinhibition and oxidative damage. In contrast, VvBEE1 inhibited Res synthesis by competing with VvHY5 for binding to the VvSTS promoter, exacerbating photodamage. The research also revealed the interaction between light signaling and brassinosteroid (BR) signaling under high light stress, indicating that the antagonistic roles of VvHY5 and VvBEE1 play a key role in regulating grapevine photoprotection mechanisms. These findings provide new insight into how plants cope with high light stress and offer potential strategies for improving crop stress tolerance. Cao et al. (2025) studied the regulatory mechanism of the FaNAC047–FaNAC058 module in heat stress-induced leaf senescence in tall fescue (Festuca arundinacea). The study found that FaNAC047 directly activated chlorophyll degradation genes (FaNYC1, FaNOL, FaSGR) and inhibited catalase gene (FaCAT2) expression, promoting chlorophyll degradation and reactive oxygen species (ROS) accumulation, thereby accelerating heat-induced leaf senescence. Additionally, FaNAC047 forms a protein complex with FaNAC058, further enhancing the regulation of downstream genes. This study reveals the critical role of the FaNAC047–FaNAC058 module in heat stress-induced leaf senescence and provides new genetic resources for breeding heat-tolerant plants.

Photosynthesis research will continue to make breakthroughs in multiple fields, driving advancements in agriculture, ecology, and renewable energy. First, with the progress of synthetic biology and gene-editing technologies, researchers can more precisely engineer photosynthetic pathways to optimize light energy utilization efficiency and carbon fixation capacity. For example, by introducing artificial photorespiration bypasses or enhancing RuBisCO activity, it is possible to significantly improve crop photosynthetic efficiency and yield, addressing global food security challenges. Second, photosynthesis research will help to understand how plants respond to environmental stresses such as high temperatures, drought, and salinity. By uncovering the photosynthetic regulatory mechanisms under various stresses, more stress-resistant crop varieties can be developed, enhancing agricultural sustainability. Additionally, photosynthesis research will provide new ideas for renewable energy development. Artificial photosynthetic systems aim to mimic natural photosynthesis, efficiently converting solar energy into hydrogen or other clean fuels. Such technologies have the potential to become important alternatives to fossil fuels, reducing greenhouse gas emissions and mitigating climate change. Finally, fundamental research on photosynthesis will deepen our understanding of the origin and evolution of life. By comparing photosynthetic mechanisms across different organisms, the evolutionary history of photosynthesis and its critical role in life evolution can be revealed. In summary, photosynthesis research has broad application prospects in agriculture, ecology, and energy, providing essential support for the sustainable development of human society.

光合作用研究进展:释放粮食安全、可再生能源和环境可持续性的潜力。
光合作用是地球上最重要的生物化学过程,也是最大规模的物质和能量转换过程。它是植物、藻类和某些细菌将光能转化为化学能的过程。通过光合作用,太阳能被用来将二氧化碳和水转化为有机物(如葡萄糖)和氧气。这一过程不仅为植物自身提供能量和生长材料,也为生态系统中其他生物提供食物和氧气。农作物通过光合作用积累的有机物是人类和动物的主要食物来源。提高光合效率可以直接提高作物产量,有助于解决全球人口增长对粮食需求的压力。光合作用也是地球碳循环的核心组成部分,有助于维持大气中二氧化碳和氧气的平衡,减轻温室效应的影响。对光合作用的研究也激发了可再生能源的发展。通过模拟光合作用的机理,设计人工光合系统,将太阳能转化为清洁能源供人类使用。关注光合作用的研究可以帮助解决与食物、能源和环境相关的人类挑战。近年来,人们对光合作用中能量吸收、转移和转化的本质进行了广泛的研究,并取得了丰硕的成果。本期关于光合作用研究的特刊包括10篇文章,包括3篇综述、5篇研究论文和2篇评论。叶绿体是光合作用发生的场所,叶绿体的生物发生是光合作用顺利进行的先决条件。Frangedakis等人(2024)探索了MpRR-MYB2和MpRR-MYB5在叶绿体生物发生中的新作用,揭示了它们与GLK和GATA转录因子的相互作用。Kushwaha等(2025)对该研究进行了评论,指出这些MYB转录因子不仅调控叶绿体发育,还影响光合作用、光呼吸和固碳相关基因的表达。虽然MYB和GLK在叶绿体生物发生中具有协同作用,但MYB不能完全取代GLK的功能。该评论还指出,MYB转录因子在植物雄性生殖器官的发育中起着重要作用。未来的研究应进一步探索MYB基因的表观遗传调控及其在逆境响应中的作用,为提高作物光合效率和产量提供新的思路。作为半自主的细胞器,叶绿体中有近3000种蛋白质是从细胞质中运输出来的。Xing等(2025)在本期特刊中综述了叶绿体蛋白输入复合物(外叶绿体-内叶绿体)及其调控机制的最新进展。他们详细介绍了TOC和TIC复合物的结构和功能,以及它们在叶绿体蛋白输入中的作用,特别是通过低温电子显微镜发现的新模型。尽管TOC复合物的组成相对保守,但TIC复合物及其相关运动蛋白的组成仍存在争议,一些来自传统模型的成分(如Tic110和Tic40)未得到最近研究的支持。文章还讨论了叶绿体蛋白质进口的质量控制和逆行信号机制,强调了泛素-蛋白酶体系统在调节蛋白质进口中的重要作用。并提出了未来的研究方向,包括探索不同物种TOC-TIC复合物的结构和功能差异以及蛋白质折叠状态对进口途径的影响。本文综述为深入了解叶绿体蛋白输入的分子机制提供了重要依据,为相关领域的进一步研究奠定了基础。叶绿素在光电转换中起着至关重要的作用。Li等人(2025)全面回顾了叶绿素生物合成途径和逆行信号网络的调控,强调了叶绿素在光合作用中的核心作用及其在植物发育和环境响应中的重要性。他们详细介绍了叶绿素合成的酶调节、转录和翻译后修饰,以及叶绿体和细胞核之间的逆行信号传导机制。通过整合最新的研究成果,他们展示了叶绿素代谢的复杂性和多样性,并指出了叶绿素代谢在合成生物学和农业方面的潜在应用。本文综述为深入了解叶绿素生物合成的调控机制,为今后的研究和应用奠定了坚实的基础。 在光合作用中实现有效的能量吸收、转移和转化的关键第一步是光收集过程。近年来,通过结构生物学的研究,对光合生物的光收集复合物的认识取得了重大进展。Huang等人(2025)报道了光合细菌Chloroflexus aurantiacus中最小的反应中心-光收集复合物(CaRC-LH)的结构,使用低温电子显微镜以3.05的分辨率分解Å。该复合物仅由七个光收集亚基组成,在反应中心的可移动醌结合位点周围形成新月形。这项研究揭示了这个最小的光收集复合体的详细组织和辅助因子的排列,解释了为什么这种细菌需要一个额外的光收集天线——叶绿体——来确保足够的光捕获。本文还探讨了该复合物与叶绿体之间的电子转移途径和结合机制,为光合作用中光捕获和能量转移的多样性提供了新的认识。这一发现不仅揭示了光合细菌的进化适应性,也为光合作用机制的研究提供了重要参考。光合作用固碳是将不稳定化学能转化为稳定化学能的关键步骤。除了C3、C4和CAM三种固定碳类型外,自然界还存在多种固定碳机制。最近,Liu et al.(2024)发表了Eleocharis vivipara的基因组,揭示了这种两栖植物在水下和陆地上分别利用C3和C4光合作用进行固碳的独特机制。Besnard(2025)评论了这一成就,指出这种光合可塑性可能是通过杂交或多倍体事件获得的,基因组重组和表观遗传调控在其C3-C4转变中起着关键作用。尽管该研究提供了重要的基因组和转录组学资源,但仍有一些问题未得到解决,如C4光合作用基因的起源和进化史。未来的系统基因组学研究有望进一步阐明这些机制,并为作物改良提供潜在的应用。核酮糖-1,5-二磷酸羧化酶/加氧酶(RuBisCO)是地球上最丰富的酶,直接决定光合作用的效率。然而,作为光合作用的关键酶,它的低效率和对氧限制的敏感性使植物的固碳效率降低。Qin等(2025)全面讨论了植物碳同化工程的进展和面临的挑战,重点关注了RuBisCO的优化和新型固碳途径的开发。作者详细介绍了定向进化、合理设计、嵌合酶和辅因子工程等策略来提高RuBisCO的催化效率。此外,本文还讨论了利用微室(如C4植物中的羧酸体和束鞘细胞)增加CO2浓度和减少光呼吸损失。尽管在实验室和模式生物中取得了一些成功,但在高等植物中实施这些工程途径仍然具有挑战性。这一综述表明,通过合成生物学和人工智能,未来有可能显著提高作物产量和光合效率,为全球气候变化和粮食安全提供解决方案。RuBisCO的加氧酶活性也限制了其有效的碳固定。Mo等(2025)通过改造光呼吸依赖的甘氨酸甜菜碱(glycine betaine, GB)生物合成途径,成功提高了水稻光合固碳效率和植株结构。研究小组将嗜盐蓝藻的甘氨酸甲基化途径(imGS)引入水稻线粒体,将光呼吸过程中产生的甘氨酸转化为GB,同时降低光呼吸中间体的水平,从而减少光呼吸过程中的碳损失,提高光合速率和碳水化合物积累。此外,imGS水稻的穗部结构得到改善,分枝数和粒数显著增加,但结实率和千粒重下降。该研究为通过线粒体光呼吸旁路提高作物光合效率和产量提供了新的策略,具有重要的应用潜力。光合生物采用各种策略来应对环境压力,以确保光合作用的顺利进行。在本期特刊中,Feng等。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Integrative Plant Biology
Journal of Integrative Plant Biology 生物-生化与分子生物学
CiteScore
18.00
自引率
5.30%
发文量
220
审稿时长
3 months
期刊介绍: Journal of Integrative Plant Biology is a leading academic journal reporting on the latest discoveries in plant biology.Enjoy the latest news and developments in the field, understand new and improved methods and research tools, and explore basic biological questions through reproducible experimental design, using genetic, biochemical, cell and molecular biological methods, and statistical analyses.
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