Including Indole-3-acetic Acid Research Articles

Multipoint recognition of domoic acid from seawater by dummy template molecularly imprinted solid-phase extraction coupled with high-performance liquid chromatography

Due to the high cost of domoic acid (DA), different carboxylic acid compounds including indole-3-acetic acid (IAA), pyrrole-2-formic acid (PFA), pyridine-2,3-dicarboxylic anhydride (PDA), trimesitinic acid (TA) and citric acid (CA) were investigated as dummy templates for the molecularly imprinted solid-phase extraction (MISPE) for selective isolation and pre-concentration of an amnesic shellfish poison (ASP), DA. The highest binding amount of the polymers towards DA was obtained when CA was used as dummy template owing to its high hydrophilicity. In addition, the “four-point” recognition site constructed by three COOH groups and a OH group in CA was also speculated to be the reason for the high binding amount of CA-MIPs and the rebinding of DA can be depend on the three COOH groups and a NH group with conformational change in the recognition process. Finally, the CA-MISPE column was chosen for DA isolation and pre-concentration and effective result was obtained with recoveries higher than 90% and relative standard deviation (RSD) less than 5% (n=3). This new polymer can be effectively applied to the monitoring and predicting the existence of trace DA.

Glutathione and glutathione-S-transferase activity in Jatropha curcas in association with pyrene degrader Pseudomonas aeruginosa PDB1 in rhizosphere, for alleviation of stress induced by polyaromatic hydrocarbon for effective rhizoremediation

The strategy of rhizosphere mediated bioremediation of Polyaromatic hydrocarbons (PAH) contaminated soil is designed around plant-bacterium symbiosis. For effective application of this strategy, it is important that the bacterium should have efficient PAH degradation ability and plant should be able to tolerate the stress induced by the contaminant. The aim of this study was to investigate the ability of bacterial isolates to degrade pyrene, in addition to promote growth of Jatropha curcas, and reduce the stress response induced by pyrene in host plant for effective rhizoremediation. Among 31 bacterial strains isolated from rhizospheric soil of contaminated sites, Pseudomonas aeruginosa PDB1 was selected based on its excellent ability to degrade pyrene (74%), chrysene and benzo-a-pyrene as estimated by GC–MS analysis, in addition to plant growth promoting attributes including indole acetic acid (IAA) release, phosphate solubilization and siderophore production, which was quantitively estimated in presence and absence of pyrene.Also, glutathione-S-transferase and catechol-2,3-dioxygenase activities were induced in this strain when grown on pyrene as sole source of carbon. Pyrene negatively affected the growth of Jatropha curcas, as 28% decrease in total biomass was observed with 80mg/Kg of pyrene, while treatment with PDB1 promoted the growth of J. curcas even in presence of pyrene. Glutathione content and glutathione-S-transferase of roots of the J. curcas was estimated in pyrene contaminated soil, and with PDB1 in presence of pyrene. The GST level increased with increase in pyrene contamination. However, GST activity was significantly in same range of the plants treated with PDB1 in presence of high dose pyrene (80mg/Kg) and plants without pyrene (control) which confirmed the effectiveness of bacteria in removal of pyrene induced stress in host plants. Therefore, P. aeruginosa PDB1 is not only efficient degrader but also potential rhizospheric bacteria for reducing the PAH stress on J. curcas, and therefore useful for rhizosphere mediated remediation of pyrene contaminated soil.

The effects of exogenous hormones on rooting process and the activities of key enzymes of Malus hupehensis stem cuttings.

Malus hupehensis is an excellent Malus rootstock species, known for its strong adverse-resistance and apomixes. In the present study, stem cuttings of M. hupehensis were treated with three types of exogenous hormones, including indole acetic acid (IAA), naphthalene acetic acid (NAA), or green growth regulator (GGR). The effects and mechanisms of exogenous hormone treatment and antioxidant enzyme activity on adventitious root formation were investigated. The results showed that the apparent morphology of the adventitious root had four stages, including root pre-emergence stage (S0), early stage of root formation (S1), massive root formation stage (S2), and later stage of root formation (S3). The suitable concentrations of the three exogenous hormones, IAA, NAA and GGR, were 100 mg·L-1, 300 mg·L-1, and 300 mg·L-1, respectively. They shortened the rooting time by 25–47.4% and increased the rooting percentages of cuttings by 0.9–1.3 times, compared with that in the control. The dispersion in S0 stage was 3.6 times of that in the S1 stage after exogenous hormone application. The earlier the third critical point (P3) appeared, the shorter the rooting time and the greater the rooting percentage of the cuttings. During rhizogenesis, the activities of three antioxidant enzymes (POD, SOD, and PPO) showed an A-shaped trend. However, peak values of enzyme activity appeared at different points, which were 9 d before the P3, P3, and the fourth critical point (P4), respectively. Exogenous hormone treatment reduced the time to reach the peak value by 18 days, although the peak values of the enzymatic activities did not significantly changed. Our results suggested that exogenous hormone treatment mainly acted during the root pre-emergence stage, accelerated the synthesis of antioxidant enzymes, reduced the rooting time, and consequently promoted root formation. The three kinds of antioxidant enzymes acted on different stages of rooting.

Gibberellic acid is selectively downregulated in response to aphid-induced gall formation

The fluid-feeding aphid Schlechtendalia chinensis (Bell) induces horned galls on its primary host, the Chinese Sumac (Rhus chinensis Mill). Horned galls are harvested for their high content of tannins, and used in a range of medical and chemical applications. Gall development is a complex and highly controlled physiological process, where the growing insect population manipulates the plant developmental programs that allow the transformation of plant tissue into a gall. In this study, we examine whether Schlechtendalia alters the balance of plant hormones in the host tree as a means to achieve gall formation. For this, we measured concentrations for a series of endogenous hormones, including indole-3-acetic acid (IAA), cytokinin (CTK), gibberellic acid (GA), abscisic acid (ABA), jasmonic acid (JA), salicylic acid (SA), and ethylene (ETH). Specifically, we conducted a time course (namely, 30, 85, 100, 115, 125, 140, 155, and 170 days from gall initiation) analysis, where we measured both gall and leaf samples representing different developmental stages that spanned an entire growing season. To correlate these hormone data with developmental parameters during gall growth, we determined gall volume, tannin content, and aphid population size for the same time points. Interestingly, tannin production rose steeply in the early stages of gall development, while the aphid population size grew little. After this single peak (day 100), tannin concentrations declined moderately and aphid population size increased from then on. This switch in population growth was accompanied by notable changes in plant hormone titers. In general, all hormones but GA were elevated in all sample types isolated from the host tree (gall, leaves near and distant from gall) when compared with samples from an uninfected tree. Most of the elevated hormones showed similar changes over time; however, GA appeared to display the opposite behavior in all samples, suggesting that GA is a key target for controlling gall growth. When tannin concentrations spiked, GA levels peaked as well, while the remaining plant hormones exhibited a decline at that time. Principle component analysis revealed distinct functional groups in our hormone cohort. This yielded three groups comprising (1) CTK, ABA, ETH, and JA, (2) IAA and SA, (3) GA. The fact that GA comprised its own group and exhibited a unique profile during gall development prompted us to examine whether exogenous GA would alter the rate of gall growth. Indeed, we found that ectopic GA significantly accelerated gall growth, and more strongly than all other hormones, consistent with the notion that controlling GA levels within the gall is crucial for stimulating gall development. We propose a model, whereby the host plant downregulates GA concentrations in an attempt to throttle gall growth, while the gall-inducing aphid population counters these attempts.

Functional Role of Bacteria from Invasive Phragmites australis in Promotion of Host Growth.

We hypothesize that bacterial endophytes may enhance the competitiveness and invasiveness of Phragmites australis. To evaluate this hypothesis, endophytic bacteria were isolated from P. australis. The majority of the shoot meristem isolates represent species from phyla Firmicutes, Proteobacteria, and Actinobacteria. We chose one species from each phylum to characterize further and to conduct growth promotion experiments in Phragmites. Bacteria tested include Bacillus amyloliquefaciens A9a, Achromobacter spanius B1, and Microbacterium oxydans B2. Isolates were characterized for known growth promotional traits, including indole acetic acid (IAA) production, secretion of hydrolytic enzymes, phosphate solubilization, and antibiosis activity. Potentially defensive antimicrobial lipopeptides were assayed for through application of co-culturing experiments and mass spectrometer analysis. B. amyloliquefaciens A9a and M. oxydans B2 produced IAA. B. amyloliquefaciens A9a secreted antifungal lipopeptides. Capability to promote growth of P. australis under low nitrogen conditions was evaluated in greenhouse experiments. All three isolates were found to increase the growth of P. australis under low soil nitrogen conditions and showed increased absorption of isotopic nitrogen into plants. This suggests that the Phragmites microbes we evaluated most likely promote growth of Phragmites by enhanced scavenging of nitrogenous compounds from the rhizosphere and transfer to host roots. Collectively, our results support the hypothesis that endophytic bacteria play a role in enhancing growth of P. australis in natural populations. Gaining a better understanding of the precise contributions and mechanisms of endophytes in enabling P. australis to develop high densities rapidly could lead to new symbiosis-based strategies for management and control of the host.

Analyses of Phytohormones in Coconut (Cocos Nucifera L.) Water Using Capillary Electrophoresis-Tandem Mass Spectrometry

Capillary electrophoresis (CE) coupled with mass spectrometry (MS) or tandem mass spectrometry (MS/MS) is reported as an alternative and potentially useful method for the simultaneous analysis of various classes of phytohormones with diversified structures, including indole-3-acetic acid (IAA), indole-3-butyric acid (IBA), abscisic acid (ABA), gibberellic acid (GA), zeatin (Z), N6-benzyladenine (BA), α-naphthaleneacetic acid (NAA) and 2,4-dichlorophenoxyacetic acid (2,4-D). The key to the CE-MS/MS analysis was based on electroosmotic flow reversal using a cationic polymer-coated capillary. Under optimum conditions, a baseline separation of eight phytohormones was accomplished within 30 min using 60 mM ammonium formate/formic acid buffer of pH 3.8 with −20 kV as the separation voltage. The accessibility of MS/MS together with the characterization by migration properties obtained by CE allows for the development of CE-MS/MS as an emerging potential method for the analysis of different classes of phytohormones in a single run. The utility of the CE-MS/MS method was demonstrated by the comprehensive screening of phytohormones in coconut (Cocos nucifera L.) water after pre-concentration and purification through solid-phase extraction (SPE) cartridge. IAA, ABA, GA and Z were detected and quantified in the purified coconut water extract sample.

Molecular identification of phytoplasmas in fasciated cacti and succulent species and associated hormonal perturbation

Fasciation, a frequent phenomenon in Cactaceae, has been attributed to various causes. The present study reports on phytoplasma-induced fasciation in Euphorbia coerulescens (Euphorbiaceae), Orbea gigantea (Asclepiadaceae), Opuntia cylindrica (Cactaceae), and Senecio stapeliiformis (Asteraceae). DNA was extracted from symptomless and fasciated tissues and amplified by nested PCR using universal primers P1/P7 followed by R16F2n/R16R2 produced amplicons of 1.2 Kb. The nucleotide sequence analyses of the amplicons indicated that fasciated plants were infected by phytoplasma. Phylogenetic analysis placed the cacti fasciation phytoplasmas in 16SrII group. The hormonal content of symptomless and fasciated tissues including indole-3-acetic acid (IAA), kinetin (Kin), N6-benzyladenine (BA), abscisic acid (ABA), and gibberellic acid (GA3) was quantified by high performance liquid chromatography (HPLC). The results indicated that fasciation in O. gigantea was correlated with the accumulation of Kin and IAA increasing five and two times, respectively, as compared to symptomless tissue. However, there was no consistent pattern of hormones in other fasciated species (E. coerulescens, O. cylindrica, and S. stapeliiformis), suggesting that different plant species might have different mechanism to develop fasciation associated with phytoplasma infection.

Molecular characterization and identification of plant growth promoting endophytic bacteria isolated from the root nodules of pea (Pisum sativum L.).

Root nodule accommodates various non-nodulating bacteria at varying densities. Present study was planned to identify and characterize the non-nodulating bacteria from the pea plant. Ten fast growing bacteria were isolated from the root nodules of cultivated pea plants. These bacterial isolates were unable to nodulate pea plants in nodulation assay, which indicate the non-rhizobial nature of these bacteria. Bacterial isolates were tested in vitro for plant growth promoting properties including indole acetic acid (IAA) production, nitrogen fixation, phosphate solubilization, root colonization and biofilm formation. Six isolates were able to produce IAA at varying level from 0.86 to 16.16 μg ml(-1), with the isolate MSP9 being most efficient. Only two isolates, MSP2 and MSP10, were able to fix nitrogen. All isolates were able to solubilize inorganic phosphorus ranging from 5.57 to 11.73 μg ml(-1), except MSP4. Bacterial isolates showed considerably better potential for colonization on pea roots. Isolates MSP9 and MSP10 were most efficient in biofilm formation on polyvinyl chloride, which indicated their potential to withstand various biotic and abiotic stresses, whereas the remaining isolates showed a very poor biofilm formation ability. The most efficient plant growth promoting agents, MSP9 and MSP10, were phylogenetically identified by 16S rRNA gene sequence analysis as Ochrobactrum and Enterobacter, respectively, with 99% similarity. It is suggested the potential endophytic bacterial strains, Ochrobactrum sp. MSP9 and Enterobacter sp. MSP10, can be used as biofertilizers for various legume and non-legume crops after studying their interaction with the host crop and field evaluation.

Determination of five endogenous hormones in wheat by high performance liquid chromatography

A high performance liquid chromatographic (HPLC) method was developed to determine the five endogenous hormones including indole-3-acetic acid (IAA), abscisic acid (ABA), gibberellic acid (GA3 ), zeatin (ZT) and salicylic acid (SA) in wheat. The separation conditions were optimized, and methanol was chosen as the extraction solvent. Then the extract was extracted by petroleum ether and ethyl acetate, and purified with the Sep-Pak C18 column. The chromatographic conditions were as follows: Eclipse XDB-C18 reversed phase column (250 mm x 4.6 mm, 5 microm), the flow rate of 1 mL/min, the injection volume of 10 microL, and the detection wavelength of 240 nm were used for the separation of SA from 14.5 min to 18 min, while the detection at 254 nm used for the separation of the others. Methanol (A) and acetic acid aqueous solution (pH 3.6) (B) were used as the mobile phases with the linear gradient set as follows: 0-7 min 20% A, 7-10 min 20% A-28% A, 10-17 min 28% A, 17-19 min 28% A-40% A, 19-35 min 40% A. The results showed that: the hormones were separated well with the recoveries of 96.9% - 98%, and the RSDs were in the range of 1.54% to 2.29%. It is a reliable method for rapid, accurate separation and determination of the endogenous hormones in wheat.

Endogenous auxins in plant growth-promoting Cyanobacteria—Anabaena vaginicola and Nostoc calcicola

Three isolates of heterocystous cyanobacteria, belonging to the genera Anabaena and Nostoc, gathered from Iranian terrestrial and aquatic ecosystems exhibited considerable growth promotion effect on several vegetables and herbaceous plants. To study the ability of these three isolates to produce auxins, three endogenous auxins, including indole-3-acetic acid (IAA), and two of its main homologues, indole-3-propionic acid and indole-3-butyric acid, were extracted and analyzed with high-performance liquid chromatography equipped with diode array detector and fluorescence detector, and the results were further confirmed with liquid chromatography–tandem mass spectrometry (LC–MS/MS) in the negative-ion mode. The dominant auxin observed in all isolates was indole-3-butyric acid (IBA) in the range of 140.10–2146.96 ng g−1 fresh weight (FW), and only small amounts of IAA (2.19–9.93 ng g−1 FW) were detected. The predominance of IBA in these strains is reported for the first time which is different from the previously reported auxin profiles in microalgae and algae with the predominance of IAA.

Dynamics of growth regulators during infection of apple leaves by Alternaria alternata apple pathotype

Alternaria blotch of apple caused by Alternaria alternata apple pathotype has a severe negative effect on apple production. It can cause tissue necrosis on leaves, young shoots and fruit. Recent studies on this pathogen have mostly focused on phytotoxicity and pathogenicity. There are few reports on the roles of signaling and metabolism in the process of infection. In this paper, a filial generation with substantial differences in resistance between individuals with similar genetic background was used as a host. An aggressive strain of A. alternate, that can complete the infection process 72 h after inoculation, served as the pathogen. A reproducible and reliable in vitro inoculation system for plant growth regulator determination was established to overcome the difficulties of inoculation of attached leaves. Alterations in growth regulator concentrations were detected, including indole-3-acetic acid (IAA), zeatin riboside (ZR), gibberellin A3 (GA3), abscissic acid (ABA) and the polyamines, putrescine (Put), spermidine (Spd) and spermine (Spm). Results indicated the plant growth regulators interacted with each other to modulate signaling and metabolic networks. A biotrophic-like phase was inferred to exist before necrosis developed. Gibberellin A3 and ABA appeared to be involved in the phase transformation from the biotrophic-like stage to the necrotrophic stage. Cytokinin, Put and Spd appeared to be related to disease resistance. This study advances our knowledge of the pathological mechanisms of Alternaria blotch on apple and provides useful resources for development of disease control and prevention.

Simultaneous determination of four plant hormones in bananas by molecularly imprinted solid-phase extraction coupled with high performance liquid chromatography

A highly selective molecularly imprinted solid-phase extraction (MISPE) combined with liquid chromatography-ultraviolet detection was developed for the simultaneous isolation and determination of four plant hormones including indole-3-acetic acid (IAA), indole-3-propionic acid (IPA), indole-3-butyric acid (IBA) and 1-naphthaleneacetic acid (NAA) in banana samples. The new molecularly imprinted microspheres (MIMs) prepared by aqueous suspension polymerization using 3-hydroxy-2-naphthoic acid and 1-methylpiperazine as mimic templates performed with high selectivity and affinity for the four plant hormones, and applied as selective sorbents of solid-phase extraction could effectively eliminate the interferences of the banana matrix. Good linearity was obtained in a range of 0.04-4.00 μg g(-1) and the recoveries of the four plant hormones at three spiked levels ranged from 78.5 to 107.7% with the relative standard deviations (RSD) of less than 4.6%. The developed MISPE-HPLC protocol obviously improved the selectivity and eliminated the effect of template leakage on quantitative analysis, and could be applied for the determination of plant hormones in complicated biological samples.

Effects of Auxins on the Production of Steroidal Alkaloids in Rapidly Proliferating Tissue and Cell Cultures of Solanum lyratum

Solanum lyratum, a rare species, is used to treat cancer, tumours and warts. Plant cell and tissue culture of S. lyratum, producing steroidal alkaloids, could be useful supplements to natural sources. To study the production of solanine, solanidine and solasodine by adding auxin-type phytohormones including indole-3-acetic acid (IAA), indole-3-butyric acid (IBA), naphthaleneacetic acid (NAA) and 2,4-dichlorophenoxyacetic acid (2,4-D) to cell and callus cultures of S. lyratum. Methanolic extracts were made from callus and cell cultures of S. lyratumand and analysed using RP C₁₈ HPLC with UV detection. 2,4-D-induced calli from roots led to a significant enhancement in solanine production with a value of 4.13 mg/g dry weight (DW). The maximal solanidine and solasodine levels of 6.26 and 7.69 mg/g DW were respectively obtained with IBA- and IAA-treated S. lyratum cells at concentrations of 1 and 5 mg/L. Auxins were found to be useful phytohormones for the production of steroidal alkaloids. The callus and cell culture system developed is simple and can hence be a method of production of steroidal alkaloids in S. lyratum and other Solanaceae species.

Improved growth performance of the mangrove Avicennia marina seedlings using a 1-aminocyclopropane-1-carboxylic acid deaminase-producing isolate of Pseudoalteromonas maricaloris

Out of 62 bacterial isolates obtained from the mangrove Avicenniamarina rhizosphere that grows along the Abu Dhabi coast, United Arab Emirates (UAE), an isolate of Pseudoalteromonas maricaloris (Wild type strain) (WT) produced relatively high levels of 1-aminocyclopropane-1-carboxylic acid (ACC) deaminase in vitro. Application of this WT strain under greenhouse conditions to A. marina seedlings significantly (P < 0.05), reduced endogenous levels of ACC in the roots and shoots, and significantly (P < 0.05) increased the levels of in planta endogenous plant growth regulators (PGRs) including indole-3-acetic acid (IAA), indole-3-pyruvic acid (IPYA), putrescine (Put), spermidine (Spd) and spermine (Spm) in roots and shoots compared with control mangrove seedlings. WT application has also significantly (P < 0.05) increased photosynthetic pigment contents, photosynthetic carbon assimilation, plant water use efficiency and promoted mangrove seedlings growth characteristics including increased dry weight and length of roots and shoots, total leaf area and the number of the side branches compared with control mangrove seedlings. In comparison, an ACC deaminase non-producing mutant strain (NPM) failed to reduce endogenous levels of ACC in the roots and shoots and also failed to increase endogenous PGRs and photosynthetic pigments and did not promote seedling growth. Both WT and NPM strains were incapable of producing in vitro detectable levels of IAA, IPYA, Gibberellic acid (GA3), zeatin (Z), Put, Spd and Spm in the culture filtrates. This study demonstrated for the first time the ability of ACC deaminase-producing bacteria to promote mangrove growth under greenhouse conditions. P. maricaloris has potential as biological inoculants to promote the growth of mangrove seedlings in afforestation programs in nutrient impoverished sediments in hyper-saline coastal areas in the UAE.

Simultaneous determination of four auxins in cyanobacterial extracts using HPLC-ESI-MS

The prokaryotic cyanobacteria are important source of structurally bioactive secondary metabolites[1]. Besides having considerable pharmacological impacts such as antibacterial, antifungal and also cytotoxicity, the potential biofertilizer activity of cyanobacteria make them an attractive alternative to chemical fertilizers. Most paddy soils have a natural population of cyanobacteria. Treatment of rice seedings with collected cyanobacteria from paddy fields of Iran showed positive growth effect in vitro [2] which could be partly attributed to the possible presence of phytohormons in their composition [3]. Herein, we report a new approach for the simultaneous determination of four important auxins including indole-3-acetic acid (IAA), indole-3-propionic acid (IPA), indole-3-butyric acid (IBA) and 1-naphthalene acetic acid (NAA) with HPLC equipped with PDA detector at 220nm after extraction of the micoalgae using ultrasonic and microwave assisted extraction. The identities of the auxins were further confirmed using liquid

Water cultured propagation of Polygonum multiflorum and dynamic changes of physiological and biochemical characteristics during adventitious roots formation

Water cultured propagation technology of Polygonum multiflorum was investigated with Rooting Powder No. 2 (ABT 2) comparison experiments, and the dynamic changes of endogenous hormones including indole acetic acid (IAA), abscisic acid (ABA), zeatin riboside (ZRs) contents and activities of indoleacetic acid oxidase (IAAO), polyphenol oxidase (PPO) were analyzed during rooting period. The results showed that rooting percentage of softwood cutting with 50 mg x L(-1) ABT2 and 10 mg x L(-1) ABT2 + 0.2% Urea + 0.2% KH2PO4 treatments was 94%, rooting percentage of softwood cuttings of control was 46% only. The adventitious rooting displayed three distinct phases i. e. root-inducing, root formation and root-elongating phases. The dynamic changes of contents of endogenous plant hormones (IAA, ABA, ZRs) and activities of IAAO, PPO tested were tightly related to the rooting process of soft-wood cuttings in P. multiflorum. During root-inducing phase the contents of IAA, ABA and ZRs decreased sharply, whereas ZRs content and IAAO activity kept higher level. IAA content reached the peak and PPO activity increased obviously during root formation phase, while IAAO activities and ABA, ZRs contents declined to minimum. During root-elongating phase PPO, IAAO activities were higher and IAA, ABA, ZRs contents kept steady. During rooting ABT2 (50 mg x L(-1)) treatment increased the content of IAA and PPO activity in cuttings, while the opposite result occurred in contents of ZRs, ABA and IAAO activity.

Simultaneous Analysis of Phytohormones in Fruits Using High-Performance Liquid Chromatography Mass Spectrometry

A method for the highly sensitive detection of some phytohormones is described. We evaluated some simple methods for the extraction and purification of phytohormones using organic solvents and high-performance liquid chromatography-mass spectrometry (LC-MS) using atmospheric pressure chemical ionization (APCI). The methodology developed was used for the simultaneous detection and quantitative determination of a series of 5 phytohormones, including indole-3-acetic acid (IAA), abscisic acid (ABA), cytokinins (CKs), gibberellins (GAs) and jasmonic acids (JAs). The detection limits ranged from 0.07 pmol for JA to 4.0 pmol for ABA. Compared with previous negative electrospray ionization-tandem mass spectrometry (ESI-MS/MS) methods, the sensitivity was found to be sufficient for the detection and analysis of the above phytohormones. This method was sufficiently sensitive to permit the measurement of the endogenous concentrations of IAA, ABA, CKs, GAs, and JAs in extracts of the “Le lectier” fruit.

Effect of different fertilization treatments on indole-3-acetic acid producing bacteria in soil

Purpose Soil microorganisms directly affect the growth of plants. Especially, plant growth-promoting rhizobacteria (PGPR) play an important role in plant growth. There are many studies about the effects of different fertilization treatments on soil microbial community structure; however, the effects on PGPR, including indole-3-acetic acid (IAA)-producing bacteria have not been previously reported. The objective of this study is to determine the effects of different types of fertilizers on IAA-producing bacteria.

Effects of phytohormones on mycelial growth and exopolysaccharide biosynthesis of medicinal mushroom Pellinus linteus

Effects of phytohormones including indole-3-acetic acid (IAA), indole-3-butyric acid (IBA) and 1-naphthaleneacetic [corrected] acid (NAA) on mycelial growth of medicinal mushroom Phellinus linteus were investigated. Under the optimal IAA, IBA and NAA concentration of 1.0, 1.5 and 5.0 mg/l, the maximal mycelial diameter reached 8.6 +/- 0.4, 7.3 +/- 2.6 and 9.0 +/- 1.0 mm, respectively. The mycelial biomass and exopolysaccharide (EPS) production with addition of 5.0 mg/l NAA in a shake flask were 6.24 +/- 0.18 g/l at 168 h and 0.86 +/-0.01 g/l at 192 h, which were enhanced by 15.98 and 56.36% compared to the control, respectively. However, the molecular weight and infrared spectrum of EPS were coincident with the control. Results indicated that NAA at the proper concentration was beneficial in stimulating mycelial growth and EPS biosynthesis, whereas it could not alter the molecular structure of EPS.

Simultaneous analysis of different classes of phytohormones in coconut ( Cocos nucifera L.) water using high-performance liquid chromatography and liquid chromatography–tandem mass spectrometry after solid-phase extraction

Coconut ( Cocos nucifera L.) water, which contains many uncharacterized phytohormones is extensively used as a growth promoting supplement in plant tissue culture. In this paper, a high-performance liquid chromatography (HPLC) method was developed for the simultaneous determination of various classes phytohormones, including indole-3-acetic acid (IAA), indole-3-butyric acid (IBA), abscisic acid (ABA), gibberellic acid (GA), zeatin (Z), N 6-benzyladenine (BA), α-naphthaleneacetic acid (NAA) and 2,4-dichlorophenoxyacetic acid (2,4-D) in young coconut water (CW). The analysis was carried out using a reverse-phase HPLC gradient elution, with an aqueous mobile phase (containing 0.1% formic acid, pH adjusted to 3.2 with triethylamine (TEA)) modified by methanol, and solute detection made at 265 nm wavelength. The method was validated for specificity, quantification, accuracy and precision. After preconcentration of putative endogenous phytohormones in CW using C 18 solid-phase extraction (SPE) cartridges, the HPLC method was able to screen for putative endogenous phytohormones present in CW. Finally, the identities of the putative phytohormones present in CW were further confirmed using independent liquid chromatography–tandem mass spectrometry (LC–MS/MS) equipped with an electrospray ionization (ESI) interface.