Pub Date : 2024-02-07DOI: 10.1007/s40626-023-00306-z
Abstract
Since antiquity, plant life and complexity have aroused the curiosity of many scholars, including aspects of plant intelligence. While historically the topic of intelligence in plants in academia has been approached with scepticism, more recently this matter has gained evidence, especially in popular science literature. Based on a systematic literature review of scientific journals, this work had two objectives: (1) to describe the history and state-of-the-art of the research on plant intelligence; (2) to evaluate whether the academic literature has followed, in quantity and profile, the current profusion of the theme in popular science vehicles. The results showed that the academic production on the subject in scientific journals, although rich in arguments that account for intelligence in plants, is still not very expressive in comparison with the popular science boost in visibility. Such evidence indicates the persistence of academic resistance to the attribution of this trait to plants. Finally, we discuss implications of this trend for science and for human-nature relationships from a philosophical standpoint.
{"title":"Plant intelligence: history and current trends","authors":"","doi":"10.1007/s40626-023-00306-z","DOIUrl":"https://doi.org/10.1007/s40626-023-00306-z","url":null,"abstract":"<h3>Abstract</h3> <p>Since antiquity, plant life and complexity have aroused the curiosity of many scholars, including aspects of plant intelligence. While historically the topic of intelligence in plants in academia has been approached with scepticism, more recently this matter has gained evidence, especially in popular science literature. Based on a systematic literature review of scientific journals, this work had two objectives: (1) to describe the history and state-of-the-art of the research on plant intelligence; (2) to evaluate whether the academic literature has followed, in quantity and profile, the current profusion of the theme in popular science vehicles. The results showed that the academic production on the subject in scientific journals, although rich in arguments that account for intelligence in plants, is still not very expressive in comparison with the popular science boost in visibility. Such evidence indicates the persistence of academic resistance to the attribution of this trait to plants. Finally, we discuss implications of this trend for science and for human-nature relationships from a philosophical standpoint. </p>","PeriodicalId":23038,"journal":{"name":"Theoretical and Experimental Plant Physiology","volume":"24 1","pages":""},"PeriodicalIF":2.6,"publicationDate":"2024-02-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139757457","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-01-29DOI: 10.1007/s40626-023-00305-0
Jana Krtková
Higher education offers unique ways to provide students with knowledge of plant biology, as well as an engaging lens through which plants may be seen and appreciated. The tremendous volume of knowledge sometimes calls for introducing a different conceptual view to students who aim to become involved in plant research and related fields. It requires stepping back to consider the plant as a whole organism, connected to other organisms within an ecosystem and as a complex living form with its own plant-specific senses. Inspired by several bestselling books in this field, I launched a Plant Senses course. When using the Plant Senses tool to teach plant biology it is challenging to prevent students from over-interpreting and projecting animal features onto the plants, yet avoid an elitist zoocentric position that denies plant capacities we cannot observe with our animal perception. My course attempts to stimulate students to see the ecological importance of plants for much of life on this planet and to draw their attention to the economic value of plants to human societies. Here, I present the structure of the course and the topics covered. Further, I discuss the potential to spread this approach to other curricula and how these different fields may benefit from implementing such a course.
{"title":"Teaching plant biology through “Plant senses”—a more engaging, holistic approach and introduction","authors":"Jana Krtková","doi":"10.1007/s40626-023-00305-0","DOIUrl":"https://doi.org/10.1007/s40626-023-00305-0","url":null,"abstract":"<p>Higher education offers unique ways to provide students with knowledge of plant biology, as well as an engaging lens through which plants may be seen and appreciated. The tremendous volume of knowledge sometimes calls for introducing a different conceptual view to students who aim to become involved in plant research and related fields. It requires stepping back to consider the plant as a whole organism, connected to other organisms within an ecosystem and as a complex living form with its own plant-specific senses. Inspired by several bestselling books in this field, I launched a Plant Senses course. When using the Plant Senses tool to teach plant biology it is challenging to prevent students from over-interpreting and projecting animal features onto the plants, yet avoid an elitist zoocentric position that denies plant capacities we cannot observe with our animal perception. My course attempts to stimulate students to see the ecological importance of plants for much of life on this planet and to draw their attention to the economic value of plants to human societies. Here, I present the structure of the course and the topics covered. Further, I discuss the potential to spread this approach to other curricula and how these different fields may benefit from implementing such a course.</p>","PeriodicalId":23038,"journal":{"name":"Theoretical and Experimental Plant Physiology","volume":"58 1","pages":""},"PeriodicalIF":2.6,"publicationDate":"2024-01-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139583496","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-01-29DOI: 10.1007/s40626-023-00304-1
Bianca Bonato, Umberto Castiello, Silvia Guerra, Qiuran Wang
Motor cognition involves the process of planning and executing goal–directed movements and recognizing, anticipating, and interpreting others’ actions. Motor cognitive functions are generally associated with the presence of a brain and are ascribed only to humans and other animal species. A growing body of evidence suggests that aneural organisms, like climbing plants, exhibit behaviors driven by the intention to achieve goals, challenging our understanding of cognition. Here, we propose an inclusive perspective under motor cognition to explain climbing plants’ behavior. We will first review our empirical research based on kinematical analysis to understand movement in pea plants. Then, we situate this empirical research within the current theoretical debate aimed at extending the principles of cognition to aneural organisms. A novel comparative perspective that considers the perception–action cycle, involving transforming perceived environmental elements into intended movement patterns, is provided.
{"title":"Motor cognition in plants: from thought to real experiments","authors":"Bianca Bonato, Umberto Castiello, Silvia Guerra, Qiuran Wang","doi":"10.1007/s40626-023-00304-1","DOIUrl":"https://doi.org/10.1007/s40626-023-00304-1","url":null,"abstract":"<p>Motor cognition involves the process of planning and executing goal–directed movements and recognizing, anticipating, and interpreting others’ actions. Motor cognitive functions are generally associated with the presence of a brain and are ascribed only to humans and other animal species. A growing body of evidence suggests that aneural organisms, like climbing plants, exhibit behaviors driven by the intention to achieve goals, challenging our understanding of cognition. Here, we propose an inclusive perspective under motor cognition to explain climbing plants’ behavior. We will first review our empirical research based on kinematical analysis to understand movement in pea plants. Then, we situate this empirical research within the current theoretical debate aimed at extending the principles of cognition to aneural organisms. A novel comparative perspective that considers the perception–action cycle, involving transforming perceived environmental elements into intended movement patterns, is provided.</p>","PeriodicalId":23038,"journal":{"name":"Theoretical and Experimental Plant Physiology","volume":"154 1","pages":""},"PeriodicalIF":2.6,"publicationDate":"2024-01-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139583839","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-01-25DOI: 10.1007/s40626-023-00303-2
Tatiane Viegas Debiasi, Adélia Carla Santos Ornelas, Dimitri Nicolau Brauco, Anderson Kikuchi Calzavara, Cristiano Medri, Edmilson Bianchini, Halley Caixeta Oliveira, José Antonio Pimenta, Renata Stolf-Moreira, Marcela Blagitz
Phenotypic plasticity occurs when plants acclimatize to contrasting conditions. Herein, we test the hypothesis that seedlings of a light-demanding species have greater phenotypic plasticity compared to seedlings of a shade-tolerant species under high irradiance. Thus, we investigate the growth, anatomical, and leaf gas exchange responses of Citharexylum myrianthum, a light-demanding species, and Poecilanthe parviflora, a shade-tolerant species, under full light and 60% shading. Under full light, the seedlings of both species were shorter, showed lower photosynthetic rates and specific leaf area, and thicker palisade parenchyma. In the same conditions, C. myrianthum showed increased number of leaves, and P. parviflora reduced leaf area and increased number of stomata and allocation of phloem and cortical parenchyma. Lower photosynthetic rates may negatively affect biomass allocation and growth, although C. myrianthum seems to show a higher tolerance to irradiance since it produced more leaves. P. parviflora seems to optimize heat dissipation, reduce water loss, and improve the allocation of photoassimilate transport and storage, which could increase performance during establishment in field conditions. The plasticity index of both species was similar. Thus, generalizations about the species plasticity and ecological group to which they belong should be avoided. Species-related responses of growth, anatomical, and gas exchange parameters were found, indicating that generalizations about the performance of functional groups should also be avoided. These findings may contribute to the success of forest restoration projects.
当植物适应对比强烈的条件时,就会产生表型可塑性。在本文中,我们验证了一个假设,即在高辐照度下,需光物种的幼苗与耐阴物种的幼苗相比具有更大的表型可塑性。因此,我们研究了需光物种 Citharexylum myrianthum 和耐阴物种 Poecilanthe parviflora 在全光照和 60% 遮光条件下的生长、解剖和叶片气体交换反应。在全光照条件下,两种植物的幼苗都较短,光合速率和比叶面积较低,栅栏状实质层较厚。在相同条件下,C. myrianthum 的叶片数量增加,而 P. parviflora 的叶片面积减少,气孔数量增加,韧皮部和皮层实质分配增加。较低的光合速率可能会对生物量分配和生长产生负面影响,不过 C. myrianthum 似乎对辐照有更强的耐受性,因为它能长出更多的叶子。P. parviflora 似乎能优化散热,减少水分损失,改善光同化物的运输和储存分配,从而提高在田间条件下的生长性能。两个物种的可塑性指数相似。因此,应避免对物种的可塑性及其所属的生态群组一概而论。生长、解剖和气体交换参数的反应与物种有关,这表明也应避免对功能群的表现一概而论。这些发现可能有助于森林恢复项目的成功。
{"title":"Irradiance triggers different morphophysiological responses in two neotropical tree seedlings with contrasting light demands","authors":"Tatiane Viegas Debiasi, Adélia Carla Santos Ornelas, Dimitri Nicolau Brauco, Anderson Kikuchi Calzavara, Cristiano Medri, Edmilson Bianchini, Halley Caixeta Oliveira, José Antonio Pimenta, Renata Stolf-Moreira, Marcela Blagitz","doi":"10.1007/s40626-023-00303-2","DOIUrl":"https://doi.org/10.1007/s40626-023-00303-2","url":null,"abstract":"<p>Phenotypic plasticity occurs when plants acclimatize to contrasting conditions. Herein, we test the hypothesis that seedlings of a light-demanding species have greater phenotypic plasticity compared to seedlings of a shade-tolerant species under high irradiance. Thus, we investigate the growth, anatomical, and leaf gas exchange responses of <i>Citharexylum myrianthum</i>, a light-demanding species, and <i>Poecilanthe parviflora</i>, a shade-tolerant species, under full light and 60% shading. Under full light, the seedlings of both species were shorter, showed lower photosynthetic rates and specific leaf area, and thicker palisade parenchyma. In the same conditions, <i>C. myrianthum</i> showed increased number of leaves, and <i>P. parviflora</i> reduced leaf area and increased number of stomata and allocation of phloem and cortical parenchyma. Lower photosynthetic rates may negatively affect biomass allocation and growth, although <i>C. myrianthum</i> seems to show a higher tolerance to irradiance since it produced more leaves. <i>P. parviflora</i> seems to optimize heat dissipation, reduce water loss, and improve the allocation of photoassimilate transport and storage, which could increase performance during establishment in field conditions. The plasticity index of both species was similar. Thus, generalizations about the species plasticity and ecological group to which they belong should be avoided. Species-related responses of growth, anatomical, and gas exchange parameters were found, indicating that generalizations about the performance of functional groups should also be avoided. These findings may contribute to the success of forest restoration projects.</p>","PeriodicalId":23038,"journal":{"name":"Theoretical and Experimental Plant Physiology","volume":"54 1","pages":""},"PeriodicalIF":2.6,"publicationDate":"2024-01-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139561673","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-01-23DOI: 10.1007/s40626-023-00300-5
Hyrandir Cabral de Melo
It is suggestive that some plant features, like the absence of specialized sensory organs to detect various environmental stimuli and their sessile and autotrophic nature, may have influenced the historically limited interest in the comprehensive understanding of their capabilities. However, scientific evidence has progressively spurred changes in this scenario by revealing unexpected and astonishing capabilities of plants. The objective of this article is to explore significant scientific discoveries that have led to a complete reshaping of certain human perceptions of plant capabilities throughout history, as well as delve into the new findings that are currently remodeling our view of them in modern times. This is illustrated by outdated notions about their growth and sexual behavior that have been surpassed, as well as by current discoveries concerning plants' capacity to detect various environmental stimuli, even without specialized organs for such purposes. Following this trajectory of reshaping perceptions, we will delve into recent revelations about diverse mechanisms through which plants exchange specific and reliable information with the organisms they interact with. The article also discusses how certain discoveries made in the past few decades concerning memory and learning capacity contribute to dismantling the notion that plants operate solely through automated and linear behaviors triggered by stimuli. Furthermore, the article draws inferences about how these paradigm shifts in our understanding of plants impact on the resolution of longstanding gaps in comprehending biological phenomena, exemplified by somatic embryogenesis, as well as how they contribute to the advancement of new technologies for plant cultivation.
{"title":"Science fosters ongoing reassessments of plant capabilities","authors":"Hyrandir Cabral de Melo","doi":"10.1007/s40626-023-00300-5","DOIUrl":"https://doi.org/10.1007/s40626-023-00300-5","url":null,"abstract":"<p>It is suggestive that some plant features, like the absence of specialized sensory organs to detect various environmental stimuli and their sessile and autotrophic nature, may have influenced the historically limited interest in the comprehensive understanding of their capabilities. However, scientific evidence has progressively spurred changes in this scenario by revealing unexpected and astonishing capabilities of plants. The objective of this article is to explore significant scientific discoveries that have led to a complete reshaping of certain human perceptions of plant capabilities throughout history, as well as delve into the new findings that are currently remodeling our view of them in modern times. This is illustrated by outdated notions about their growth and sexual behavior that have been surpassed, as well as by current discoveries concerning plants' capacity to detect various environmental stimuli, even without specialized organs for such purposes. Following this trajectory of reshaping perceptions, we will delve into recent revelations about diverse mechanisms through which plants exchange specific and reliable information with the organisms they interact with. The article also discusses how certain discoveries made in the past few decades concerning memory and learning capacity contribute to dismantling the notion that plants operate solely through automated and linear behaviors triggered by stimuli. Furthermore, the article draws inferences about how these paradigm shifts in our understanding of plants impact on the resolution of longstanding gaps in comprehending biological phenomena, exemplified by somatic embryogenesis, as well as how they contribute to the advancement of new technologies for plant cultivation.</p>","PeriodicalId":23038,"journal":{"name":"Theoretical and Experimental Plant Physiology","volume":"4 1","pages":""},"PeriodicalIF":2.6,"publicationDate":"2024-01-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139561641","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-01-06DOI: 10.1007/s40626-023-00299-9
André G. Daubermann, Valéria F. Lima, Alexander Erban, Joachim Kopka, Alisdair R. Fernie, Markus Schwarzländer, Leticia dos Anjos, Danilo M. Daloso
The tricarboxylic acid (TCA) cycle is an important metabolic pathway to underpin stomatal movements, given that respiration is thought to be the main energy source for guard cell (GC) metabolism. However, it is still unclear how the metabolic fluxes throughout the TCA cycle and associated pathways are regulated in GCs. Here we used a 13C-positional isotopomer approach and performed a multi-species/cell-types analysis based on previous 13C-labelling studies carried out using Arabidopsis rosettes, maize leaves, Arabidopsis source and sink leaves, and isolated GCs from Arabidopsis and tobacco. We aimed to compare flux modes through the TCA cycle and associated pathways in GCs and leaves, which are mostly composed by mesophyll cells (MCs). Mesophyll cells showed high 13C-enrichment into alanine and aspartate following provision of 13CO2, whilst GCs and sink MCs showed high 13C-incorporation into glutamate/glutamine following provision of 13C-sucrose. Only GCs showed high 13C-enrichment in the carbon 1 atom of glutamine, which is derived from phosphoenolpyruvate carboxylase (PEPc)-mediated CO2 assimilation. The PEPc-mediated 13C-incorporation into malate was similar between GCs and MCs, but GCs had higher 13C-enrichment and accumulation of fumarate than MCs. The metabolic fluxes throughout the TCA cycle of illuminated GCs resemble those of sink MCs, but with different contribution from PEPc, glycolysis and the TCA cycle to glutamate/glutamine synthesis. We further demonstrate that transamination reactions catalysed by alanine and aspartate amino transferases may support non-cyclic TCA flux modes in illuminated MCs.
{"title":"Novel guard cell sink characteristics revealed by a multi-species/cell-types meta-analysis of 13C-labelling experiments","authors":"André G. Daubermann, Valéria F. Lima, Alexander Erban, Joachim Kopka, Alisdair R. Fernie, Markus Schwarzländer, Leticia dos Anjos, Danilo M. Daloso","doi":"10.1007/s40626-023-00299-9","DOIUrl":"https://doi.org/10.1007/s40626-023-00299-9","url":null,"abstract":"<p>The tricarboxylic acid (TCA) cycle is an important metabolic pathway to underpin stomatal movements, given that respiration is thought to be the main energy source for guard cell (GC) metabolism. However, it is still unclear how the metabolic fluxes throughout the TCA cycle and associated pathways are regulated in GCs. Here we used a <sup>13</sup>C-positional isotopomer approach and performed a multi-species/cell-types analysis based on previous <sup>13</sup>C-labelling studies carried out using Arabidopsis rosettes, maize leaves, Arabidopsis source and sink leaves, and isolated GCs from Arabidopsis and tobacco. We aimed to compare flux modes through the TCA cycle and associated pathways in GCs and leaves, which are mostly composed by mesophyll cells (MCs). Mesophyll cells showed high <sup>13</sup>C-enrichment into alanine and aspartate following provision of <sup>13</sup>CO<sub>2</sub>, whilst GCs and sink MCs showed high <sup>13</sup>C-incorporation into glutamate/glutamine following provision of <sup>13</sup>C-sucrose. Only GCs showed high <sup>13</sup>C-enrichment in the carbon 1 atom of glutamine, which is derived from phospho<i>enol</i>pyruvate carboxylase (PEPc)-mediated CO<sub>2</sub> assimilation. The PEPc-mediated <sup>13</sup>C-incorporation into malate was similar between GCs and MCs, but GCs had higher <sup>13</sup>C-enrichment and accumulation of fumarate than MCs. The metabolic fluxes throughout the TCA cycle of illuminated GCs resemble those of sink MCs, but with different contribution from PEPc, glycolysis and the TCA cycle to glutamate/glutamine synthesis. We further demonstrate that transamination reactions catalysed by alanine and aspartate amino transferases may support non-cyclic TCA flux modes in illuminated MCs.</p>","PeriodicalId":23038,"journal":{"name":"Theoretical and Experimental Plant Physiology","volume":"91 1","pages":""},"PeriodicalIF":2.6,"publicationDate":"2024-01-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139373405","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2024-01-06DOI: 10.1007/s40626-023-00302-3
Abstract
Proline is an amino acid acting as an osmoprotector in plants, as it reduces osmotic potential and enhances plant water uptake, especially under drought. Aluminum (Al) toxicity causes inhibition of root growth and low leaf hydration with negative consequences for photosynthetic performance. Thus, plants under Al toxicity could benefit from proline accumulation. Here we investigated whether proline is induced by Al in Pinus sylvestris, an Al-tolerant woody species. Proline and abscisic acid (ABA) concentration, gas exchange rates, stomatal conductance (gs), relative needle water content (RWC), stem water potential (Ψw), biometric data and plant biomass were evaluated in plants grown in nutrient solution with 0, 250, 500, and 1000 μM Al for 42 days. Plant growth, gas exchange rates, RWC and ABA were the same between the four treatments, as expected for an Al-tolerant species. The maintenance of needle hydration throughout the study provides a plausible explanation for the similar gas exchange values observed between Al-treated and untreated plants. Over the course of 7 to 14 days, plants exposed to Al showed a decrease in midday stem water potential (Ψmd), and an increase in proline concentration. Subsequently, both parameters exhibited similar values between treatments until the end of the study. These findings suggest proline may play a role in osmotic adjustment in P. sylvestris exposed to Al.
摘要 脯氨酸是一种氨基酸,在植物体内起着渗透保护作用,因为它能降低渗透势,提高植物的吸水能力,尤其是在干旱条件下。铝(Al)毒性会抑制根系生长,降低叶片水合作用,对光合作用产生负面影响。因此,铝毒性下的植物可以从脯氨酸的积累中获益。在此,我们研究了耐铝的木本植物 Pinus sylvestris 是否会受到铝的诱导而产生脯氨酸。在含有 0、250、500 和 1000 μM Al 的营养液中生长 42 天的植物,其脯氨酸和脱落酸(ABA)浓度、气体交换速率、气孔导度(gs)、针叶相对含水量(RWC)、茎干水势(Ψw)、生物计量数据和植物生物量均得到了评估。植物的生长、气体交换率、RWC 和 ABA 在四种处理之间是相同的,这也是耐铝物种的预期结果。在整个研究过程中,针叶的水合作用一直保持不变,这也是铝处理植物和未处理植物气体交换值相似的一个合理解释。在 7 到 14 天的过程中,暴露于铝的植物显示出正午茎干水势(Ψmd)的下降和脯氨酸浓度的上升。随后,直到研究结束,这两个参数在不同处理之间表现出相似的值。这些研究结果表明,脯氨酸可能在暴露于 Al 的西洋芹的渗透调节中发挥作用。
{"title":"Does aluminum induce high proline concentration in Pinus sylvestris, an Al-tolerant species?","authors":"","doi":"10.1007/s40626-023-00302-3","DOIUrl":"https://doi.org/10.1007/s40626-023-00302-3","url":null,"abstract":"<h3>Abstract</h3> <p>Proline is an amino acid acting as an osmoprotector in plants, as it reduces osmotic potential and enhances plant water uptake, especially under drought. Aluminum (Al) toxicity causes inhibition of root growth and low leaf hydration with negative consequences for photosynthetic performance. Thus, plants under Al toxicity could benefit from proline accumulation. Here we investigated whether proline is induced by Al in <em>Pinus sylvestris</em>, an Al-tolerant woody species. Proline and abscisic acid (ABA) concentration, gas exchange rates, stomatal conductance (<em>gs</em>), relative needle water content (RWC), stem water potential (Ψw), biometric data and plant biomass were evaluated in plants grown in nutrient solution with 0, 250, 500, and 1000 μM Al for 42 days. Plant growth, gas exchange rates, RWC and ABA were the same between the four treatments, as expected for an Al-tolerant species. The maintenance of needle hydration throughout the study provides a plausible explanation for the similar gas exchange values observed between Al-treated and untreated plants. Over the course of 7 to 14 days, plants exposed to Al showed a decrease in midday stem water potential (Ψmd), and an increase in proline concentration. Subsequently, both parameters exhibited similar values between treatments until the end of the study. These findings suggest proline may play a role in osmotic adjustment in <em>P. sylvestris</em> exposed to Al.</p>","PeriodicalId":23038,"journal":{"name":"Theoretical and Experimental Plant Physiology","volume":"3 1","pages":""},"PeriodicalIF":2.6,"publicationDate":"2024-01-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139373459","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2023-12-15DOI: 10.1007/s40626-023-00301-4
Dhara Arora, Neha Singh, Satish C. Bhatla
Modulation of melatonin signaling pathway occurs either by direct interaction with calmodulin (CaM) or through regulation of intracellular Ca2+ concentration. Intracellular CaM and CaM-dependent phosphodiesterase (PDE) activity are also possibly modulated by melatonin in vitro through melatonin-CaM interaction. Melatonin acts as a CaM antagonist and modulates CaM-dependent protein phosphorylation, thereby rhythmically regulating cellular functions. Melatonin also acts as a nitric oxide synthase (NOS) inhibitor by interfering with CaM binding to NOS peptide, thereby inhibiting NO biosynthesis. CaM also inhibits the effects of melatonin on cyclic GMP biosynthesis. Melatonin can cause increase in reactive oxygen species (ROS) generation through CaM–mediated activation of phospholipase A2 (PLA2). Thus, the prooxidant action of melatonin is mediated through CaM. Melatonin can directly scavenge ROS species and regulate the activities of various antioxidant enzymes though interaction with CaM. Melatonin causes microtubule depolymerization, thereby affecting cytoskeleton organization in the cells. CaM also inhibits tubulin polymerization. Melatonin is known to regulate photoperiodism and circadian rhythmicity in plants. Both salt stress and melatonin seem to modulate seedling growth by inhibiting CaM-mediated calcium signaling. Upregulation of genes encoding CaM-like protein, calcium-binding protein, calcium-dependent phosphodiesterase and CBL (calcineurin B-like proteins)-interacting protein kinase indicates possible calcium-mediated melatonin signaling in plants.
{"title":"Calmodulin and calcium-mediated melatonin signaling mechanisms in plants","authors":"Dhara Arora, Neha Singh, Satish C. Bhatla","doi":"10.1007/s40626-023-00301-4","DOIUrl":"https://doi.org/10.1007/s40626-023-00301-4","url":null,"abstract":"<p>Modulation of melatonin signaling pathway occurs either by direct interaction with calmodulin (CaM) or through regulation of intracellular Ca<sup>2+</sup> concentration. Intracellular CaM and CaM-dependent phosphodiesterase (PDE) activity are also possibly modulated by melatonin in vitro through melatonin-CaM interaction. Melatonin acts as a CaM antagonist and modulates CaM-dependent protein phosphorylation, thereby rhythmically regulating cellular functions. Melatonin also acts as a nitric oxide synthase (NOS) inhibitor by interfering with CaM binding to NOS peptide, thereby inhibiting NO biosynthesis. CaM also inhibits the effects of melatonin on cyclic GMP biosynthesis. Melatonin can cause increase in reactive oxygen species (ROS) generation through CaM–mediated activation of phospholipase A<sub>2</sub> (PLA<sub>2</sub>). Thus, the prooxidant action of melatonin is mediated through CaM. Melatonin can directly scavenge ROS species and regulate the activities of various antioxidant enzymes though interaction with CaM. Melatonin causes microtubule depolymerization, thereby affecting cytoskeleton organization in the cells. CaM also inhibits tubulin polymerization. Melatonin is known to regulate photoperiodism and circadian rhythmicity in plants. Both salt stress and melatonin seem to modulate seedling growth by inhibiting CaM-mediated calcium signaling. Upregulation of genes encoding CaM-like protein, calcium-binding protein, calcium-dependent phosphodiesterase and CBL (calcineurin B-like proteins)-interacting protein kinase indicates possible calcium-mediated melatonin signaling in plants.</p>","PeriodicalId":23038,"journal":{"name":"Theoretical and Experimental Plant Physiology","volume":"34 1","pages":""},"PeriodicalIF":2.6,"publicationDate":"2023-12-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"138683530","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2023-12-14DOI: 10.1007/s40626-023-00298-w
Gustavo Resende Rios, C. Rios, T. O. de Araújo, A. I. Siqueira-Silva, E. G. Pereira
{"title":"Iron excess and nitrogen deprivation influence photosynthetic metabolism in grasses used for mineland rehabilitation","authors":"Gustavo Resende Rios, C. Rios, T. O. de Araújo, A. I. Siqueira-Silva, E. G. Pereira","doi":"10.1007/s40626-023-00298-w","DOIUrl":"https://doi.org/10.1007/s40626-023-00298-w","url":null,"abstract":"","PeriodicalId":23038,"journal":{"name":"Theoretical and Experimental Plant Physiology","volume":"229 1","pages":""},"PeriodicalIF":2.6,"publicationDate":"2023-12-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"138975578","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2023-12-12DOI: 10.1007/s40626-023-00297-x
João Alves Ferreira Pereira, Mônica Maria de Almeida Lopes, Carlos Farley Herbster Moura, Thais Andrade Germano, José Hélio Costa, Maria Raquel Alcântara de Miranda
This study evaluated gene expression and activity of key enzymes associated with L-ascorbic acid metabolism during the development of acerola. Acerola cv. Flor-branca shows a double sigmoid growth curve reaching physiological maturity at 17 days after anthesis (DAA) and is fully ripe at 21 DAA. Thus, fruits were analyzed at 15, 17, 19, 21 and 23 DAA. Total L-ascorbic acid (T-AsA) concentration declined 60% from immature green (15 DAA) to the fully ripe stage (21 DAA), with a relative increase in the content of the reduced form L-ascorbic acid (AsA). Regarding AsA biosynthesis, L-GalLDH activity increased during fruit development from 15 to 19 DAA. Oxidative enzyme activity patterns differed during ripening, APX was initially higher and decreased, while ascorbate oxidase (AO) activity was initially lower and then increased until 21 DAA. The activity patterns of recycling enzymes monodehydroascorbate reductase (MDHAR), dehydroascorbate reductase (DHAR) and glutathione reductase (GR) were similar and increased during fruit development. The genes associated with AsA biosynthesis (GalLDH, GMP and GME) showed similar expression profiles during fruit maturation (after 17 DAA) and may be related to the increase in L-GalLDH activity. The profile of genes linked to AsA degradation showed that AO isoform 2 is mainly involved in oxidation during fruit development. The high concentration of T-AsA in immature acerola seems related to cellular intake from phloem due to the high expression of the l-ascorbic acid transporter NAT3 gene. The data observed here gives an insight into the key points of regulation of AsA metabolism during acerola development that enables further fresh market and industrial uses, besides genetic manipulation efforts.