Physiologia plantarum最新文献

Cold stress (CS) is a significant natural hazard, and distinguishing between plant cold resistance and sensitivity is critical for cultivar breeding and the development of germplasm resources. This study used 205 tobacco (Nicotiana tabacum L.) varieties from around the world to investigate the changes in the chlorophyll a fluorescence (OJIP) transients, JIP-test parameters, and seedling growth caused by seven days of CS (5°C) treatment. Their cold resistance was assessed using the cold-resistant coefficient, derived from the relative growth rate of shoots, damage scores, and JIP-test parameters. The results showed that total electron carriers per reaction center (S_m) and relative variable fluorescence at the I-step (V_I) were better indicators of cold resistance than maximum quantum yield of photochemistry at t = 0 (F_v/F_m), which was widely used to assess plant cold resistance. Next, the study examined the effects of CS and subsequent recovery on OJIP transients, JIP-test parameters, and seedling growth in two highly resistant (HR) and two highly sensitive (HS) varieties to confirm the reliability of the assessment methods. The results indicated that HR varieties experienced less photoinhibitory damage to photosystem II, exhibited lower growth inhibition during CS, and showed better recovery during the recovery period compared to HS varieties. These findings suggested that the JIP-test parameters could serve as a reliable tool for assessing tobacco cold resistance and aid in selecting varieties with enhanced resilience to CS.

Populus tree species are commonly used for creating shelter forests in vast areas of northern China, at least partially due to their fast growth. However, they are facing severe problems of decline and mortality caused by drought. In contrast, tree species native to water-limited environments usually have slow growth and are currently not commonly used in afforestation, while these species are gaining more attention in forestry for their greater resilience to drought. In Horqin Sandy Land, we conducted a comparative analysis of xylem hydraulics and associated physiological traits between six Populus tree species and six tree species native to drought-prone areas. Compared to the native species, the Populus species exhibited significantly higher stem hydraulic conductivity but lower resistance to drought-induced xylem embolism than the native tree species. The observed interspecific variations and contrasts in xylem hydraulics between the two species groups were predominantly attributed to xylem anatomical characteristics at the pit level rather than at the tissue level. In line with the divergences in hydraulics, we found significantly lower intrinsic water use efficiency (WUE_i) in Populus than in the native species, suggesting that the two groups adopted relatively acquisitive and conservative water use strategies, respectively. The trade-off between hydraulic efficiency and safety, as well as that between hydraulic efficiency and WUE_i, underlies the contrasts in performance between Populus species and the native tree species, that is, fast growth of Populus species but high risk of hydraulic dysfunction when facing drought, and vice versa.

The relative performance of rhizobial strains could depend on their resource allocation, environmental conditions, and host genotype. Here, we used a high-throughput shoot phenotyping to investigate the effects of Mesorhizobium strain on the growth dynamics, nodulation and bacteroid traits with four chickpea (Cicer arietinum) varieties grown under different water regimes in an experiment including four nitrogen sources (two Mesorhizobium strains, and two uninoculated controls: nitrogen fertilised and unfertilised) under well-watered and drought conditions. We asked three questions. Does the impact of rhizobial strains on chickpea growth change with well-watered versus drought conditions? Do Mesorhizobium strains differ in their ability to influence biomass and nodule traits of chickpea varieties under well-watered and drought conditions? Are bacteroid size and amount of polyhydroxybutyrate modified by Mesorhizobium strain, chickpea variety, water availability and their interactions? Under well-watered conditions, chickpea inoculated with CC1192 showed higher shoot growth rates than M075 and accumulated high plant biomass at harvest. Under drought conditions, however, the shoot growth rate was comparable between CC1192 and M075, with no significant difference in plant biomass and symbiotic effectiveness at harvest. Across sources of variation, plant biomass varied 3.0-fold, nodules per plant 3.9-fold, nodule dry weight 3.0-fold, symbiotic effectiveness 1.5-fold, bacteroid size 1.4-fold and bacteroid polyhydroxybutyrate 1.4-fold. Plant biomass was negatively correlated with both bacteroid size and allocation to polyhydroxybutyrate under well-watered conditions, suggesting a trade-off between plant and rhizobial fitness. This study demonstrates the need to reassess rhizobial strain effectiveness across diverse environments, recognising the dynamic nature of their interaction with host plants.

Flowering time is a critical determinant of plant reproductive success and agricultural yield. Hydrogen sulfide (H₂S), as a signaling molecule, regulates various aspects of plant growth and development. In this study, we examined the role of endogenous H₂S in regulating flowering time in Arabidopsis. The O-acetylserine thiol lyase a1 (oasa1) mutant, which has elevated H₂S levels due to impaired OASA1 activity that catalyzes the synthesis of Cys from H₂S, flowers earlier than wild type (WT). The OASA1 overexpression lines (OE-OASA1-#33/#142), characterized by reduced H₂S levels, show delayed flowering, accompanied by decreased expression of key flowering regulators, FLOWERING LOCUS T (FT), SUPPRESSOR OF OVEREXPRESSION OF CONSTANS1 (SOC1), and AGAMOUS-LIKE24 (AGL24). Notably, vernalization and short-day (SD) conditions did not affect their flowering patterns. Exogenous H₂S and GA₃ treatment rescued the delayed flowering phenotype of OE-OASA1-#33/#142. In oasa1, levels of GA intermediates (GA₁₅ and GA₅₃) were elevated, while their levels were reduced in OE-OASA1-#33/#142. RT-qPCR analysis showed a significant reduction in the expression of GIBBERELLIN 20-OXIDASE 4 (GA20ox4) in OE-OASA1-#33/#142 compared to WT. Overexpression of GA20ox4 (OE-GA20ox4-#20/#30) resulted in earlier flowering and partially rescued the delayed flowering phenotype of OE-OASA1-#33/#142. Additionally, the expression of age pathway-related genes, including miRNA172b and SQUAMOSA PROMOTER BINDING PROTEIN-LIKE 3/4/5/9/15 (SPL3/4/5/9/15), was significantly reduced in OE-OASA1-#33/#142 seedlings. These findings suggest that endogenous H₂S positively regulates GA20ox4 expression, thereby promoting gibberellin synthesis and advancing flowering in Arabidopsis through the GA pathway. Furthermore, the promotion of flowering by H₂S appears to be linked to the age pathway.

In many plant species, the application of exogenous phytohormones is crucial for initiating de novo shoot regeneration. However, ipecac [Carapichea ipecacuanha (Brot) L. Andersson] has a unique ability to develop adventitious shoots on the epidermis of internodal segments without phytohormone treatment. This characteristic allows us to evaluate the effects of endogenous phytohormones in this species. Here, we showed that the presence of the pith, including vascular bundles in the internodal segment, is required to activate both endogenous cytokinin (CK) biosynthesis and adventitious shoot formation. Adventitious shoots were mainly formed in the apical region of internodal segments, where the CK biosynthesis genes ISOPENTENYL TRANSFERASE 3 (CiIPT3) and LONELY GUY 7 (CiLOG7) were spontaneously upregulated in the early culture stage on phytohormone-free medium. In addition, CiIPT3 and CiLOG7 were respectively expressed in the pith and the epidermis of the internodal segments. The expression of CiLOG7 was localized as several spots on the epidermis. These findings suggest that CK precursors are generated in the pith, transferred to the epidermis, and then converted into active CKs, facilitating adventitious shoot formation on the epidermis. Conversely, auxin levels rapidly decreased during culture and remained low in the region of shoot formation. Auxin is transferred to the basal region of internodal segments, and strongly suppressed the CiLOG7 expression and decreased the CK levels. Thus, we conclude that the ectopic expression of CiLOG7 in the epidermis of internodal segments contributes to de novo shoot regeneration in ipecac.

Stone cells are one of the limiting factors affecting pear fruit quality and commodity value. The formation of stone cell is highly correlated with lignin deposition. However, the molecular mechanism of stone cell formation and regulation is still unclear. Here, we observed that exogenous application of GA significantly inhibited the formation of stone cells and also decreased the content of lignin in 'Nanguo' (Pyrus ussuriensis) pear fruits. The key gene PuPRX73 involved in the lignin synthesis pathway was further identified using RT-PCR, and GA-treatment significantly inhibited the expression of PuPRX73. Overexpression or silencing of PuPRX73 in pear fruits significantly increases or decreases the content of stone cells and lignin. We identified the transcription factors PuMYB91 and PuERF023 using mRNA-seq and their expression was significantly decreased after GA-treatment. Transient overexpression of PuMYB91 and PuERF023 promotes lignin and stone cells content in pear fruits, while silencing of PuMYB91 and PuERF023 led to the opposite results and inhibited the expression of PuPRX73. Yeast one-hybrid (Y1H) and GUS activity analysis revealed that PuMYB91 and PuERF023 directly bind and activate the PuPRX73 promoter, and co-transfection of PuMYB91 and PuERF023 in Nicotiana benthamiana leaves further promoted the promoter activity of PuPRX73. Furthermore, we found that PuMYB91 interacted with PuERF023 in vitro by using Yeast two-hybrid assays (Y2H). In conclusion, our results revealed that exogenous GA-treatment inhibits stone cell production by suppressing the expression of PuMYB91 and PuERF023 in pear fruits.

Phosphorus (P) deficiency is a critical factor limiting crop productivity, primarily due to its detrimental effects on photosynthesis and dry matter accumulation. In this study, we investigate the role of the rice gene OsPHT2;1 in mediating chloroplast P homeostasis and its subsequent impact on photosynthetic function under low P conditions. Stomatal conductance is typically positively correlated with net photosynthetic rates; however, P deficiency disrupts this relationship, leading to reduced stomatal opening and diminished photosynthetic efficiency. Our findings show that the OsPHT2;1 mutation leads to a decrease in the plastoquinone (PQ) pool size. This change is associated with altered stomatal conductance and modifications in electron transport dynamics, including an increase in the transmembrane proton gradient and a shift from linear to cyclic electron transport. This disruption significantly impairs the transport of photosynthetic products, particularly triose phosphates, essential for sucrose synthesis in the cytoplasm. Additionally, the reduced PQ pool influences the expression of key genes involved in photostability, highlighting the interplay between P homeostasis and photosynthetic regulation. By elucidating the mechanisms underlying OsPHT2;1's role in chloroplast function, our research underscores its significance in optimizing rice adaptation to low P environments, thereby enhancing crop resilience and productivity.

Photosynthetic microalgae are promising green cell factories for the sustainable production of high-value chemicals and biopharmaceuticals. The chloroplast organelle is being developed as a chassis for synthetic biology as it contains its own genome (the plastome) and some interesting advantages, such as high recombinant protein titers and a diverse and dynamic metabolism. However, chloroplast engineering is currently hampered by the lack of standardized cloning tools and Design-Build-Test-Learn workflows to ease genomic and metabolic engineering. The MoClo (Modular Cloning) toolkit based on Golden Gate assembly was recently developed in the model eukaryotic green microalgae Chlamydomonas reinhardtii to facilitate nuclear transformation and engineering. Here, we present MoCloro as an extension of the MoClo that allows chloroplast genome engineering. Briefly, a Golden Gate-compatible chloroplast transformation vector (pWF.K.4) was constructed, which contains homologous arms for integration at the petA site in the plastome. A collection of standardized parts (promoters, terminators, reporter and selection marker genes) was created following the MoClo syntax to enable easy combinatorial assembly of multi-cassettes in the destination pWF.K.4 vector. The functionality of the biobricks was assayed by constructing and assessing the expression of several multigenic constructs. Finally, a generic vector pK4 was constructed for easy Golden Gate cloning of 5' and 3' homologous arms, allowing targeting at alternative plastome integration sites. This work represents a significant advancement in technology aimed at facilitating more efficient and rapid chloroplast transformation and engineering of green microalgae.

Auxins play a critical role in several plant developmental processes and their endogenous levels are regulated at multiple levels. The enzymes of the GRETCHEN HAGEN 3 (GH3) protein family catalyze the conjugation of amino acids to indoleacetic acid (IAA), the major endogenous auxin. The GH3 proteins are encoded by multiple redundant genes in plant genomes, making it difficult to perform functional genetic studies to understand their role in auxin homeostasis. To address these challenges, we used a chemical approach that exploits the reaction mechanism of GH3 proteins to identify small molecule inhibitors of their activity from a defined chemical library. The study evaluated receptor-ligand complexes based on their binding energy and classified them accordingly. Docking algorithms were used to correct any deviations, resulting in a list of the most important inhibitory compounds for selected GH3 enzymes based on a normalized sum of energy. The study presents atomic details of protein-ligand interactions and quantifies the effect of several of the identified small molecule inhibitors on auxin-mediated root growth processes in Arabidopsis thaliana. The direct effect of these compounds on endogenous auxin levels was measured using appropriate auxin sensors and endogenous hormone measurements. Our study has identified novel compounds of the flavonoid biosynthetic pathway that are effective inhibitors of GH3 enzyme-mediated IAA conjugation. These compounds play a versatile role in hormone-regulated plant development and have potential applications in both basic research and agriculture.