Indole-3-acetic Acid Research Articles

Agronomic Effectiveness of Zinc Sources as Micronutrient Fertilizers: A Comprehensive Review’

Zinc naturally occurs in the earth's crust as part of rocks and ore minerals. The average concentration of zinc in the lithosphere is 80 mg kg-1. While zinc is relatively immobile in soil, it is moderately mobile in plants. As a vital micronutrient for both humans and animals, zinc plays an essential role in plants as a catalytic, structural and regulatory cofactor for many enzyme reactions. It is necessary for the metabolism of carbohydrates, protein synthesis, the biosynthesis of growth hormones (particularly indoleacetic acid) and the maintenance of cell membrane integrity. Zinc deficiency is a widespread problem affecting both plants and humans in many regions of the world. To address this issue and improve plant zinc nutrition and yields, both soil and foliar zinc fertilizers have been applied. The agronomic effectiveness of Zn fertilizers has been related to the management factors such as placement, source type, seed treatment, foliar spray and biofortification that can affect the effectiveness of Zn fertilizers.

Promising antifungal behavior of biosynthesized bimetallic silver-copper oxide nanoparticles and Bacillus safensis against some strawberry rots

Promising nanomaterials combined with beneficial microbes contributed to bio-modulations that might increase yields. In order to combat several fungal infections that invade strawberries (Fragaria ananassa), this study assessed the interactions between the synthesized CuO NPs, bimetallic Ag–CuO NPs, and Bacillus safensis (BS-22) under various treatment circumstances. The effectiveness of BS-22, CuO NPs, and bimetallic Ag–CuO NPs against four different pathogens that cause gray mold disease and root rot on strawberry plants was determined. It was possible to successfully extract twenty-four endophytic bacterial isolates from hygienic strawberry plants that were indigenous. BS-22 isolate, which produced the most hydrogen cyanide (HCN), siderophores, gibberellic acid (GA3), and indole-3-acetic acid (IAA), was identified molecularly as Bacillus safensis. The most extensively studied treatments (foliar CuO NPs at 200 ppm + foliar Ag–CuO NPs at 200 ppm + BS-22) decreased the frequency and severity of black root rot disease in strawberry plants. Foliar CuO NPs (50 ppm) + foliar Ag–CuO NPs (50 ppm) showed significant increase of the total suspended solids (TSSs), total antioxidant capacity (TAC) content, and the total polyphenols content compared to the control and other treatments. The same treatment recorded the highest value in all characters of cell wall components except lignin character where BS-22 treatment had the best effect. All tested treatments significantly decreased disease incidence and severity when strawberry fruit stored at 22 °C ± 2 for 25 days on average. According to this study, foliar CuO NPs (200 ppm) + foliar Ag–CuO NPs (200 ppm) + BS-22 (as a soil drench) might be used as a substitute for gray mold and root rot diseases in strawberry development and biocontrol.

Targeted HER2-positive cancer therapy using ADAPT6 fused to horseradish peroxidase

Targeted cancer therapy is a promising alternative to the currently established cancer treatments, aiming to selectively kill cancer cells while sparing healthy tissues. Hereby, molecular targeting agents, such as monoclonal antibodies, are used to bind to cancer cell surface markers specifically. Although these agents have shown great clinical success, limitations still remain such as low tumor penetration and off-target effects. To overcome this limitation, novel fusion proteins comprised of the two proteins ADAPT6 and Horseradish Peroxidase (HRP) were engineered. Cancer cell targeting is hereby enabled by the small scaffold protein ADAPT6, engineered to specifically bind to human epidermal growth factor receptor 2 (HER2), a cell surface marker overexpressed in various cancer types, while the enzyme HRP oxidizes the nontoxic prodrug indole-3-acetic acid (IAA) which leads to the formation of free radicals and thereby to cytotoxic effects on cancer cells. The high affinity to HER2, as well as the enzymatic activity of HRP, were still present for the ADAPT6-HRP fusion proteins. Further, in vitro cytotoxicity assay using HER2-positive SKOV-3 cells revealed a clear advantage of the fusion proteins over free HRP by association of the fusion proteins directly to the cancer cells and therefore sustained cell killing. This novel strategy of combining ADAPT6 and HRP represents a promising approach and a viable alternative to antibody conjugation for targeted cancer therapy.

The involvement of phytohormones in plant–pathogen interaction

Plant–pathogen interactions involve intricate signaling networks that coordinate the plant immune response. Recognition of pathogens through pattern recognition receptors (PRRs) triggers activation of mitogen-activated protein kinase (MAPK) pathways, initiating a cascade of defense mechanisms. Central to these responses is the synthesis of phytohormones such as salicylic acid (SA), auxins–indole-3-acetic acid (IAA), and gibberellins–gibberellic acid (GA), pivotal for immune activation. This review explores the multifaceted roles of these phytohormones in plant immunity, drawing on recent findings from Arabidopsis thaliana and Gossypium hirsutum studies. The review discusses MAPK-mediated activation of TGA1/4 (TGACG sequence-specific binding protein 1/4) transcription factors enhancing SA biosynthesis via isochorismate synthase (ICS). Increased SA levels activate NPR1, promoting gene expression in immune-related pathways including systemic acquired resistance (SAR). Concurrently, pathogen-induced IAA synthesis activates auxin-responsive genes crucial for immune responses. Elevated biosynthesis of IAA from L-tryptophan activates these genes by degrading repressor molecules. IAA acts antagonistically to SA, conserving energy during pathogen infection. Additionally, GA is vital for plant growth and development, operating DELLA (Asp–Glu–Leu–Leu–Ala) protein degradation with the formation of a complex with gibberellin insensitive dwarf 1 (GID1). Once DELLA prevents releasing GA-related response reactions, it is extremelly crucial for GA actions. In general, the review explores the intricate interplay between SA, IAA, and GA, highlighting SA's antagonistic regulation of GA signaling and the synergistic effects of auxin and GA. Understanding these hormone–mediated pathways is crucial for elucidating precise mechanisms underlying plant immunity. Insights gained could inform strategies to enhance plant resistance against pathogens, contributing to sustainable agriculture and global food security efforts.

The functional identification and evaluation of endophytic bacteria sourced from the roots of tolerant Achyranthes bidentata to overcome monoculture problems of Rehmannia glutinosa.

The isolation and identification of plant growth-promoting endophytic bacteria (PGPEB) from Achyranthes bidentata roots have profound theoretical and practical implications in ecological agriculture, particularly as bio-inoculants to address challenges associated with continuous monoculture. Our research revealed a significant increase in the abundance of these beneficial bacteria in A. bidentata rhizosphere soil under prolonged monoculture conditions, as shown by bioinformatics analysis. Subsequently, we isolated 563 strains of endophytic bacteria from A. bidentata roots. Functional characterization highlighted diverse plant growth-promoting traits among these bacteria, including the secretion of indole-3-acetic acid (IAA) ranging from 68.01 to 73.25 mg/L, phosphorus and potassium solubilization capacities, and antagonistic activity against pathogenic fungi (21.54%-50.81%). Through 16S rDNA sequencing, we identified nine strains exhibiting biocontrol and growth-promoting potential. Introduction of a synthetic microbial consortium (SMC) in pot experiments significantly increased root biomass by 48.19% in A. bidentata and 27.01% in replanted Rehmannia glutinosa. These findings provide innovative insights and strategies for addressing continuous cropping challenges, highlighting the practical promise of PGPEB from A. bidentata in ecological agriculture to overcome replanting obstacles for non-host plants like R. glutinosa, thereby promoting robust growth in medicinal plants.

The auxin-responsive CsSPL9-CsGH3.4 module finely regulates auxin levels to suppress the development of adventitious roots in tea (Camellia sinensis).

The cutting technique is extensively used in tea breeding, with key emphasis on promoting the growth of adventitious roots (ARs). Despite its importance in tea cultivation, the mechanisms underlying AR development in tea remain unclear. In this study, we demonstrated the essential role of auxins in the initiation and progression of AR and established that the application of exogenous 1-naphthaleneacetic acid-enhanced AR formation in tissue-cultured seedlings and cuttings. Then, we found that the auxin-responsive transcription factor CsSPL9 acted as a negative regulator of AR development by reducing the levels of free indole-3-acetic acid (IAA) in tea plants. Furthermore, we identified CsGH3.4 as a downstream target of CsSPL9, which was activated by direct binding to its promoter. CsGH3.4 also inhibited AR development and maintained low levels of free IAA. Thus, these results revealed the inhibitory effect of the auxin-responsive CsSPL9-CsGH3.4 module on AR development by reducing free IAA levels in tea. These findings have significant theoretical and practical value for enhancing tea breeding practices.

Enhancement of in situ detection and imaging of phytohormones in plant tissues by MALDI-MSI using 2,4-dihydroxy-5-nitrobenzoic acid as a novel matrix.

Phytohormones possess unique chemical structures, and their physiological effects are regulated through intricate interactions or crosstalk among multiple phytohormones. MALDI-MSI enables the simultaneous detection and imaging of multiple hormones. However, its application for tracing phytohormones is currently restricted by low abundance of hormone in plant and suboptimal matrix selection. 2,4-Dihydroxy-5-nitrobenzoic acid (DHNBA) was reported as a new MALDI matrix for the enhanced detection and imaging of multiple phytohormones in plant tissues. DHNBA demonstrates remarkable sensitivity improvement when compared to the commonly used matrix, 2,5-dihydroxybenzoic acid (DHB), in the detection of isoprenoid cytokinins (trans-zeatin (tZ), dihy-drozeatin (DHZ), meta-topolin (mT), and N6-(Δ2-isopentenyl) adenine (iP)), jasmonic acid (JA), abscisic acid (ABA), and 1-aminocyclo-propane-1-carboxylic acid (ACC) standards. The distinctive properties of DHNBA (i.e. robust UV absorption, uniform matrix deposition, negligible background interference, and high ionization efficiency of phytohormones) make it as an ideal matrix for enhanced detection and imaging of phytohormones, including tZ, DHZ, ABA, indole-3-acetic acid (IAA), and ACC, by MALDI-MSI in various plant tissues, for example germinating seeds, primary/lateral roots, and nodules. Employing DHNBA significantly enhances our capability to concurrently track complex phytohormone biosynthesis pathways while providing precise differentiation of the specific roles played by individual phytohormones within the same category. This will propel forward the comprehensive exploration of phytohormonal functions in plant science.

Plant growth promotion activities of Bacillus spp. isolated from Jakrem hot water spring of Meghalaya, North East India

The study aims to investigate plant growth promotion (PGP) activities of thermophilic bacteria isolated from the Jakrem hot spring in Meghalaya, North-East India, and determine their effect on Brassica juncea's growth. The bacteria were isolated by a culture-dependent approach following a serial dilution method in a nutrient agar medium. All the isolates were determined for PGP attributes such as indole acetic acid, phosphate solubilization, hydrolytic enzymes, and siderophore production. The potent bacterial isolates were characterized by 16S rDNA sequencing and phylogenetic analysis. Altogether, 53 bacterial isolates were obtained, most belonging to the genus Bacillus. Of the total isolates, 37.7% exhibited both PGP and hydrolytic enzyme activities. Three isolates, namely JAB1, JAB8, and JAB100, showed promising PGP and were identified as Bacillus velezensis, B. proteolyticus, and Bacillus sp., respectively. The PGP attributes of these isolates were determined in vivo on B. juncea, and their effects were measured in terms of shoot and root length biomass and biochemical contents. It was observed that combined inoculation of all three isolates significantly enhanced the growth and development of B. juncea, evident by increased shoot and root length, fresh and dry weight, and higher levels of protein, phenol, flavonoid, and chlorophyll content compared to the control. In conclusion, the study highlights the potential application of thermophilic Bacillus spp. from hot springs as bioinoculants to enhance crop productivity in sustainable agricultural practices.

6-shogaol against 3-Nitropropionic acid-induced Huntington's disease in rodents: Based on molecular docking/targeting pro-inflammatory cytokines/NF-κB-BDNF-Nrf2 pathway.

Huntington's disease (HD) is an extremely harmful autosomal inherited neurodegenerative disease. Motor dysfunction, mental disorder, and cognitive deficits are the characteristic features of this disease. The current study examined whether 6-shogaol has a protective effect against 3-Nitropropionic Acid (3-NPA)-induced HD in rats. A total of thirty male Wistar rats received 6-shogaol (10 and 20 mg/kg, per oral) an hour before injection of 3-NPA (10 mg/kg i.p.) for 15 days. Behavioral tests were performed, including narrow beam walk, rotarod test, and grip strength test. Biochemical tests promoting oxidative stress were evaluated [superoxide dismutase (SOD), reduced glutathione (GSH), catalase (CAT) and malondialdehyde (MDA)], including changes to neurotransmitters serotonin (5-HT), dopamine (DA), norepinephrine (NE), homovanillic acid (HVA), (3,4-dihydroxyphenylacetic acid (DOPAC), γ-aminobutyric acid (GABA), and 5-hydroxy indole acetic acid (5-HIAA), nuclear factor kappa-B (NF-κB), tumor necrosis factor-α (TNF-α), interleukins-1β (IL-1β), IL-6, brain-derived neurotrophic factor (BDNF), and nuclear factor erythroid 2-related factor 2 (Nrf2). The 6-shogaol was docked to the active site of TNF-α (2AZ5), NF-κB (1SVC), BDNF) [1B8M], and Nrf2 [5FZN] proteins using AutoDock tools. The 6-shogaol group significantly improved behavioral activity over the 3-NPA-injected control rats. Moreover, 3-NPA-induced significantly altered neurotransmitters, biochemical and neuroinflammatory indices, which could efficiently be reversed by 6-shogaol. The 6-shogaol showed favorable negative binding energies at -9.271 (BDNF) kcal/mol. The present investigation demonstrated the neuroprotective effects of 6-shogaol in an experimental animal paradigm against 3-NPA-induced HD in rats. The suggested mechanism is supported by immunohistochemical analysis and western blots, although more research is necessary for definite confirmation.

Enhancing content and decreasing production costs of phycocyanin through phytohormone supplementation in Spirulina cultivations

This study explores the potential of fractional supplementation of the phytohormone indole-3-acetic acid (IAA) to enhance phycocyanin production in Spirulina cultures. Microalgae cultures were supplemented with IAA at specific time points (days 0, 5, 10, 15, 20, and 25), reaching the same supplementation concentration (0.1 mg L−1) in the final 30-day cultivation period. The continuous daily supplementation resulted in a remarkable 229 % (106.41 mg g−1) increase in phycocyanin concentration and a 251 % (8.3 mg L−1 d−1) improvement in productivity compared to the control group without phytohormone addition (32.30 mg g−1 and 2.4 mg L−1 d−1, respectively). Additionally, the strategy successfully reduced the production cost of the pigment by 71 %. This approach can potentially make microalgae-based products more accessible to the population while addressing the industry's need for cost-effective pigment production. The study offers a novel strategy for optimizing natural pigment production and microalgae cultivation.

OsMYB14, an R2R3-MYB transcription factor, regulates plant height through the control of hormone metabolism in rice

Plant growth must be regulated throughout the plant life cycle. The myeloblastosis (MYB) transcription factor (TF) family is one of the largest TF families and is involved in metabolism, lignin biosynthesis, and developmental processes. Here, we showed that OsMYB14, a rice R2R3-MYB TF, was expressed in leaves and roots, especially in rice culm and panicles, and that it localized to the nucleus. Overexpression of OsMYB14 (OsMYB14-ox) in rice resulted in a 30% reduction in plant height compared to that of the wild type (WT), while the height of the osmyb14-knockout (osmyb14-ko) mutant generated using the CRISPR/Cas9 system was not significantly different. Microscopic observations of the first internode revealed that the cell size did not differ significantly among the lines. RNA sequencing analysis revealed that genes associated with plant development, regulation, lipid metabolism, carbohydrate metabolism, and gibberellin (GA) and auxin metabolic processes were downregulated in the OsMYB14-ox line. Hormone quantitation revealed that inactive GA19 accumulated in OsMYB14-ox but not in the WT or knockout plants, suggesting that GA20 generation was repressed. Indole-3-acetic acid (IAA) and IAA-aspartate accumulated in OsMYB14-ox and osmyb14-ko, respectively. Indeed, real-time PCR analysis revealed that the expression of OsGA20ox1, encoding GA20 oxidase 1, and OsGH3-2, encoding IAA-amido synthetase, was downregulated in OsMYB14-ox and upregulated in osmyb14-ko. A protein-binding microarray revealed the presence of a consensus DNA-binding sequence, the ACCTACC-like motif, in the promoters of the OsGA20ox1 and GA20ox2 genes. These results suggest that OsMYB14 may act as a negative regulator of biological processes affecting plant height in rice by regulating GA biosynthesis and auxin metabolism.

Exploring the biocontrol and plant growth-promoting potential of Streptomyces kronopolitis isolate SA18 against durian foliar blight and dieback disease

Abstract. Kraivuttinun P, Pirapak K, Pinnak P, Pirapak W. 2024. Exploring the biocontrol and plant growth-promoting potential of Streptomyces kronopolitis isolate SA18 against durian foliar blight and dieback disease. Biodiversitas 25: 2661-2669. Actinomycetes have been extensively studied for their potential as plant growth promoters and biocontrol agents against fungal plant pathogens. In Thailand, durian is a highly valuable fruit crop, celebrated for its delectable fleshy arils. Rhizoctonia solani destruction causes foliar blight and dieback, a severe disease on durian plantations. Our investigation objective was to isolate, select, and identify actinomycetes that exhibit antagonistic properties and could improve the growth of durian. This study revealed that 37 actinomycete isolates were obtained, comprising 14 endophytic isolates and 23 soil-derived actinomycete isolates from durian plantations in Thailand's Uttaradit and Sukhothai Provinces. All actinomycete isolates demonstrated the ability to inhibit pathogen growth through in vitro antagonistic bioassay. Isolate SA18 exhibited the highest percentage inhibition of radial growth against R. solani isolate 01, achieving an impressive 92% inhibition. Furthermore, isolate SA18 demonstrated the capacity to produce 5.91 ?g/mL of indole acetic acid after seven days of culture, increasing to 45.72 ?g/mL after 14 days. This isolate also exhibited phosphate solubilization ability. In the detached leaf bioassay, isolate SA18 effectively controlled the spread of fungal pathogens, reducing disease severity significantly from 93.75% in the control treatment to 53.75% with a concentration of 108 spores/mL of isolate SA18. Morphological examination and 16S rRNA gene sequencing revealed that isolate SA18 formed smooth-surfaced spores in chains and showed a close relationship with Streptomyces kronopolitis based on the 16S rDNA sequence. This study is the first to report the presence of S. kronopolitis in soil samples collected from durian orchards in Thailand. This isolate can improve plant growth and control R. solani in bioassays. S. kronopolitis isolate SA18 can potentially be a biocontrol agent for durian plantations.

A Comprehensive Approach Combining Short-Chain Polyphosphate and Bacterial Biostimulants for Effective Nutrient Solubilization and Enhanced Wheat Growth.

Phosphorus constitutes a crucial macronutrient for crop growth, yet its availability often limits food production. Efficient phosphorus management is crucial for enhancing crop yields and ensuring food security. This study aimed to enhance the efficiency of a short-chain polyphosphate (PolyP) fertilizer by integrating it with plant growth-promoting bacteria (PGPB) to improve nutrient solubilization and wheat growth. Specifically, the study investigated the effects of various bacterial strains on wheat germination and growth when used in conjunction with PolyP. To achieve this, a greenhouse experiment was conducted in which the wheat rhizosphere was amended with a short-chain PolyP fertilizer. Based on the morphological aspect, eight bacteria, designated P1 to P8, were isolated and further characterized. Plant growth-promoting traits were observed in all bacterial strains, as they presented the ability to produce Indole Acetic Acid (IAA) in significant amounts ranging from 7.5 ± 0.3 µg/mL to 44.1 ± 2 µg/mL, expressed by B. tropicus P4 and P. soyae P1, respectively. They also produced ammonia, hydrogen cyanide (HCN), and siderophores. Their effect against the plant pathogen Fusarium culmorum was also assessed, with P. reinekei P2 demonstrating the highest biocontrol activity as it presented a total inhibitory effect. Additionally, some strains exhibited the ability to solubilize/hydrolyze phosphorus, potassium, and zinc. In vivo, the initial growth potential of wheat seeds indicated that those inoculated with the isolated strains exhibited elevated germination rates and enhanced root growth. Based on their plant growth-promoting traits and performance in the germination assay, three strains were selected for producing the best results, specifically phosphorus hydrolyzation/solubilization, zinc solubilization, IAA production, HCN, and siderophores production. Wheat seeds were inoculated by drenching in a bacterial suspension containing 1010 CFU/mL of log phase culture, and an in planta bioassay was conducted in a growth chamber using three selected strains (Pseudomonas soyae P1, Pseudomonas reinekei P2, and Bacillus tropicus P4), applied either individually or with PolyP on a P-deficient soil (28 mg/kg of P Olsen). Our findings demonstrated that the combination of Pseudomonas soyae P1 and PolyP achieved the highest shoot biomass, averaging 41.99 ± 0.87 g. Notably, applying P. soyae P1 or Bacillus tropicus P4 alone yielded similar results to the use of PolyP alone. At the heading growth stage, the combination of Bacillus tropicus P4 and PolyP significantly increased the Chlorophyll Content Index (CCI) to 37.02 µmol/m2, outperforming both PolyP alone (24.07 µmol/m2) and the control (23.06 µmol/m2). This study presents an innovative approach combining short-chain PolyP with bacterial biostimulants to enhance nutrient availability and plant growth. By identifying and characterizing effective bacterial strains, it offers a sustainable alternative to conventional fertilizers.

Adaptive Responses of Hormones to Nitrogen Deficiency in Citrus sinensis Leaves and Roots.

Some citrus orchards in China often experience nitrogen (N) deficiency. For the first time, targeted metabolomics was used to examine N-deficient effects on hormones in sweet orange (Citrus sinensis (L.) Osbeck cv. Xuegan) leaves and roots. The purpose was to validate the hypothesis that hormones play a role in N deficiency tolerance by regulating root/shoot dry weight ratio (R/S), root system architecture (RSA), and leaf and root senescence. N deficiency-induced decreases in gibberellins and indole-3-acetic acid (IAA) levels and increases in cis(+)-12-oxophytodienoic acid (OPDA) levels, ethylene production, and salicylic acid (SA) biosynthesis might contribute to reduced growth and accelerated senescence in leaves. The increased ethylene formation in N-deficient leaves might be caused by increased 1-aminocyclopropanecarboxylic acid and OPDA and decreased abscisic acid (ABA). N deficiency increased R/S, altered RSA, and delayed root senescence by lowering cytokinins, jasmonic acid, OPDA, and ABA levels and ethylene and SA biosynthesis, increasing 5-deoxystrigol levels, and maintaining IAA and gibberellin homeostasis. The unchanged IAA concentration in N-deficient roots involved increased leaf-to-root IAA transport. The different responses of leaf and root hormones to N deficiency might be involved in the regulation of R/S, RSA, and leaf and root senescence, thus improving N use efficiency, N remobilization efficiency, and the ability to acquire N, and hence conferring N deficiency tolerance.

Transcriptome and Metabolome Analyses of Leaves from Cutting Rejuvenation of Ancient Cinnamomum camphora.

Rejuvenation refers to the transition from the state of mature to juvenile. Many ancient Cinnamomum camphora have aged and died due to climatic and anthropic factors. Vegetative propagation can protect valuable germplasm resources. In this study, a 2000-year-old ancient C. camphora and its 2-year-old cutting plantlets were selected as experimental materials. The results indicated that the number of leaves with palisade tissue (Pal) cell layers was different between samples, with two layers in the rejuvenated leaves (RLs) and one layer in the mature leaves (MLs) and young leaves (YLs). Indole-3-acetic acid (IAA), isopentenyladenine (iP) and isopentenyladenosine (iPR) concentrations were significantly higher in RLs than in MLs and YLs, but the abscisic acid (ABA) concentration was lower. Targeted metabolome analysis identified 293 differentially accumulated metabolites (DAMs). Meanwhile, a total of 5241 differentially expressed genes (DEGs) were identified by transcriptome sequencing. According to the KEGG analysis, there were seven important enriched pathways in the MLs, RLs and YLs, including plant hormone signal transduction (57 DEGs), plant-pathogen interaction (56 DEGs) and MAPK signaling pathway-plant (36 DEGs). KEGG enrichment conjoint analyses of DEGs and DAMs identified 16 common pathways. Integrated analyses of cytological, hormone, metabolome and transcriptome elements can provide a research basis in regard to the rejuvenation regulatory mechanism of ancient C. camphora.

An Efficient In Vitro Shoot Organogenesis and Comparative GC-MS Metabolite Profiling of Gaillardia pulchella Foug

Gaillardia pulchella Foug. is a widely studied plant because of its high pharmacological and ornamental value. The leaves of G. pulchella were used for inducing callus and subsequent plant regeneration as it is the primary source of phytocompounds. The purpose of the present investigation was to formulate an in vitro propagation method for Gaillardia by using leaf explants in MS (Murashige and Skoog) medium. The best callus induction was observed on high (2.0 mg/L) α-naphthalene acetic acid (NAA) and a low (0.5 mg/L) 6-benzylaminopurine (BAP) with callus induction frequency of 91.66%. The leaf callus also demonstrated high caulogenesis ability (95.83%), with an average 5.2 shoots/callus mass at 0.5 mg/L BAP and 2.0 mg/L NAA. Indole Acetic acid (IAA) at 1.0 mg/L had the maximum rooting percentage (79.17%) with 12.4 roots per shoot. Rooted plantlets were later transferred to greenhouse conditions, showing a survivability rate of 75–80%. The physiological parameters, i.e., phenolic compounds and the flavonoids’ level, in the DPPH assay were higher in leaves obtained in vitro compared to callus formed from leaves and field-obtained (mother) leaves. Gas chromatography–mass spectrometry (GC–MS) analysis of methanol extracts of leaves (in vivo and in vitro) and leaf callus presented a wide array of compounds. In callus extract, some 34 phytocompounds were identified. Some of them were 3-hydroxy-2,3-dihydromaltol (25.39%), isoamyl acetate (11.63%), palmitic acid (11.55%), 4-methyloxazole (7.54%), and 5-methoxypyrrolidin-2-one (7.49%). Leaves derived in vivo and in vitro had 45 and 28 phytocompounds, respectively, belonging to different classes like lignans, phenols, terpenoids, alkaloids and fatty acids, etc. Those findings demonstrated that the leaf derived callus and the leaves are the potential stable source of several compounds with medicinal importance. The developed protocol may provide an alternative source of compounds without affecting wild flora.

Dynamic Changes of Phytohormone Concentrations during <i>Prunella vulgaris</i> L. Development and Impact of Rosmarinic Acid Accumulation through Exogenous ABA Application

Background: Plant hormones not only participate in regulating the growth and development process of plants, but also play an important regulatory role in the synthesis of secondary metabolites. Prunella vulgaris L. (P. vulgaris) is a perennial herb that has a long history for use as a kind of medicinal and edible plant. In order to understand the relationship between plant hormones and Prunella vulgaris L. (P. vulgaris) development. Methods: The quantification of indoleacetic acid (IAA), salicylic acid (SA), jasmonates (JAs), abscisic acid (ABA), 1-aminocyclopropane-1-carboxylic acid (ACC) and cytokinins (CKs) of P. vulgaris during development was performed by a liquid chromatography-mass spectrometry (LC-MS). Furthermore, the effect of exogenous ABA on rosmarinic acid (RA) accumulation was verified. Results: Nuts formation was related to the concentrations of IAA, ABA and ACC in the green-fruit stage, and IAA and ABA levels increased rapidly in this stage. High IAA concentrations can promote an increase in ACC. SA, JAs, ethylene (ET) and ABA were related to the defence response of plants to pathogens. SA concentrations increased sharply after the turning stage, while the concentration of JAs, which are antagonistic to SA, was low. The decrease in ABA concentration after this period may be related to the antagonistic effect of IAA or SA. The CKs trans-zeatin (tZ) and trans-zeatin riboside (tZR) promoted the growth and development of early P. vulgaris, and their concentrations decreased in the late period, leading to withering and senescence of P. vulgaris. The CKs cis-zeatin (cZ) and N6-(2-isopentenyl) adenine (iP) were presumed to be present in nuts. After elicitation with 10 μg/mL ABA, an increase of RA content was observed (p < 0.05). Conclusion: This study can provide an improved basis for elucidating the growth and development mechanism of P. vulgaris in the future, as well as a better understand of the effects of ABA application on RA accumulations.

Enhancing Sugarcane Seedling Resilience to Water Stress through Exogenous Abscisic Acid: A Study on Antioxidant Enzymes and Phytohormone Dynamics.

Exogenous hormones play a crucial role in regulating plant growth, development, and stress tolerance. However, the effects of exogenous abscisic acid (ABA) on sugarcane seedlings under water stress remain poorly understood. Here, in this study, a pot experiment was conducted on sugarcane seedlings 4 weeks after transplanting, employing three treatments: control (normal growth), drought (water stress), and drought + ABA (foliar application of 100 μM ABA before water stress). The main objectives of this research are to understand the effects of exogenous ABA on sugarcane seedlings under water stress conditions and to assess the changes in antioxidant enzyme activity and phytohormone levels in response to exogenous ABA. Water stress was induced in the solution culture by adding 25% (w/v) polyethylene glycol (PEG) 6000 to the Hoagland solution. Leaf samples were collected at 3, 6, and 9 days after treatment, and the photosynthetic and biochemical responses of ABA-treated plants to drought stress were investigated. The indole acetic acid (IAA) activity of the ABA-treated drought plants is compared to that of drought plants. Moreover, the endogenous ABA levels of the ABA-treated drought plants were significantly enhanced by 42.2, 39.9, and 42.3% at 3, 6, and 9 days, respectively, compared to those of drought plants. Additionally, the proline content of the ABA-treated drought plants significantly increased by 45 and 80% at 6 and 9 days, respectively, compared to that of drought plants. The expression of the catalase 1 (CAT1) gene was increased in the ABA-treated drought plants by 2.1-fold, 0.7-fold, and 1.37-fold at 3, 6, and 9 days, respectively, compared to that in drought plants. Similarly, the expression of superoxide dismutase, peroxidase, and ascorbate peroxidase genes of the ABA-treated drought plants also increased compared to those of the drought plants. In conclusion, foliar application of ABA mitigated the negative effects of water shortage of sugarcane plants under water stress. Applying ABA improved the antioxidant defense system of sugarcane plants under drought stress, thereby enhancing their photosynthetic activities and productivity.

Efficient In Vitro Regeneration System and Comparative Transcriptome Analysis Offer Insight into the Early Development Characteristics of Explants from Cotyledon with Partial Petiole in Small-Fruited Pepper (Capsicum annuum).

In our research, we utilized six small-fruited pepper germplasms as materials, selected cotyledons with the petiole and hypocotyls as explants, and conducted in vitro regeneration studies. Our outcomes specify that the most suitable explant is cotyledon with the petiole, and the suitable genotype is HNUCA341. The optimal medium for inducing and elongating adventitious buds for this genotype is Murashige and Skoog medium (MS) + 9.12 μM Zeatin (ZT) + 0.57 μM 3-Indoleacetic acid (IAA), with a bud induction rate of 44.4%. The best rooting induction medium is MS + 1.14 μM IAA, with a rooting rate of 86.7%. Research on the addition of exogenous hormones has revealed that the induction speed of buds in small-fruited pepper (HNUCA341) in the combination of ZT and IAA hormones (abbreviated as ZI) is quicker, and the induction effect is better. The histological observations indicate that ZI treatment accelerates the initiation of explant division and differentiation, causing a shorter duration of vascular-bundle tissue production. The plant hormone signaling pathway was significantly enriched by Kyoto Encyclopedia of Genes and Genomes (KEGG) analysis, including ARR9 (LOC107843874, LOC107843885), ARR4 (LOC107848380, LOC107862455), AHK4 (LOC107870540), AHP1 (LOC107839518), LAX2 (LOC107846008), SAUR36 (LOC107852624), IAA8 (LOC107841020), IAA16 (LOC107839415), PYL4 (LOC107843441), and PYL6 (LOC107871127); these significantly enriched genes may be associated with in vitro regeneration. In addition, the carbon metabolism pathway and plant mitogen-activated protein kinase (MAPK) signaling pathway are also significantly enriched in KEGG. The results of the Gene Ontology (GO) analysis revealed that differentially expressed genes related to carbon metabolism and fixation, photosynthesis and MAPK signaling pathways were upregulated under ZI treatment. It was found that they might be associated with enhanced regeneration in vitro. Furthermore, we also screened out differentially expressed transcription factors, primarily from the MYB, bHLH, AP2/ERF, and NAC families. Overall, our work accumulated important data for the in-depth analysis of the molecular mechanism of in vitro regeneration of pepper, and provides valuable germplasm for establishing an efficient stable pepper genetic-transformation system based on tissue culture.

Indole-3-acetic acid enhances the co-transport of proton and phenanthrene mediated by TaSAUR80-5A in wheat roots

Polycyclic aromatic hydrocarbons (PAHs) are a type of organic pollution that can accumulate in crops and hazard human health. This study used phenanthrene (PHE) as a model PAH and employed hydroponic experiments to illustrate the role of indole-3-acetic acid (IAA) in the regulation of PHE accumulation in wheat roots. At optimal concentrations, wheat roots treated with PHE + IAA showed a 46.9% increase in PHE concentration, whereas treatment with PHE + P-chlorophenoxyisobutyric acid resulted in a 38.77% reduction. Transcriptome analysis identified TaSAUR80-5A as the crucial gene for IAA-enhancing PHE uptake. IAA increases plasma membrane H+-ATPase activity, promoting active transport of PHE via the PHE/H+ cotransport mechanism. These results provide not only the theoretical basis necessary to better understand the function of IAA in PAHs uptake and transport by staple crops, but also a strategy for controlling PAHs accumulation in staple crops and enhancing phytoremediation of PAH-contaminated environments.