GA Production Research Articles

The SINA1-BSD1 Module Regulates Vegetative Growth Involving Gibberellin Biosynthesis in Tomato.

In plants, vegetative growth is controlled by synergistic and/or antagonistic effects of many regulatory factors. Here, the authors demonstrate that the ubiquitin ligase seven in absentia1 (SINA1) mammalian BTF2-like transcription factors, Drosophila synapse-associated proteins, and yeast DOS2-like proteins (BSD1) function as a regulatory module to control vegetative growth in tomato via regulation of the production of plant growth hormone gibberellin (GA). SINA1 negatively regulates the protein level of BSD1 through ubiquitin-proteasome-mediated degradation, and the transgenic tomato over-expressing SINA1 (SINA1-OX) resembles the dwarfism phenotype of the BSD1-knockout (BSD1-KO) tomato plant. BSD1 directly activates expression of the BSD1-regulated gene 1 (BRG1) via binding to a novel core BBS (standing for BSD1 binding site) binding motif in the BRG1 promoter. Knockout of BRG1 (BRG1-KO) in tomato also results in a dwarfism phenotype, suggesting BRG1 plays a positive role in vegetative growth as BSD1 does. Significantly, GA contents are attenuated in transgenic SINA1-OX, BSD1-KO, and BRG1-KO plants exhibiting dwarfism phenotype and exogenous application of bioactive GA3 restores their vegetative growth. Moreover, BRG1 is required for the expression of multiple GA biosynthesis genes and BSD1 activates three GA biosynthesis genes promoting GA production. Thus, this study suggests that the SINA1-BSD1 module controls vegetative growth via direct and indirect regulation of GA biosynthesis in tomato.

Fungal Diversity and Gibberellin Hormones Associated with Long Whips of Smut-Infected Sugarcanes.

Sugarcane smut, caused by the fungus Sporisorium scitamineum (Sydow), significantly affects sugarcane crops worldwide. Infected plants develop whip-like structures known as sori. Significant variations in these whip lengths are commonly observed, but the physiological and molecular differences causing these morphological differences remain poorly documented. To address this, we employed conventional microbe isolation, metagenomic, and metabolomic techniques to investigate smut-infected sugarcane stems and whips of varying lengths. Metagenomics analysis revealed a diverse fungal community in the sugarcane whips, with Sporisorium and Fusarium genera notably present (>1%) in long whips. Isolation techniques confirmed these findings. Ultra-performance liquid chromatography analysis (UHPLC-MS/MS) showed high levels of gibberellin hormones (GA3, GA1, GA4, GA8, and GA7) in long whips, with GA4 and GA7 found exclusively in long whips and stems. Among the prominent genera present within long whips, Fusarium was solely positively correlated with these gibberellin (GA) hormones, with the exception of GA8, which was positively correlated with Sporisorium. KEGG enrichment analysis linked these hormones to pathways like diterpenoid biosynthesis and plant hormone signal transduction. These findings suggest that Fusarium may influence GA production leading to whip elongation. Our study reveals fungal dynamics and gibberellin responses in sugarcane smut whips. Future research will explore the related molecular gibberellin synthesis mechanisms.

Cell factories for biosynthesis of D-glucaric acid: a fusion of static and dynamic strategies.

D-glucaric acid is an important organic acid with numerous applications in therapy, food, and materials, contributing significantly to its substantial market value. The biosynthesis of D-glucaric acid (GA) from renewable sources such as glucose has garnered significant attention due to its potential for sustainable and cost-effective production. This review summarizes the current understanding of the cell factories for GA production in different chassis strains, from static to dynamic control strategies for regulating their metabolic networks. We highlight recent advances in the optimization of D-glucaric acid biosynthesis, including metabolic dynamic control, alternative feedstocks, metabolic compartments, and so on. Additionally, we compare the differences between different chassis strains and discuss the challenges that each chassis strain must overcome to achieve highly efficient GA productions. In this review, the processes of engineering a desirable cell factory for highly efficient GA production are just like an epitome of metabolic engineering of strains for chemical biosynthesis, inferring general trends for industrial chassis strain developments.

The GA and ABA signaling is required for hydrogen-mediated seed germination in wax gourd

BackgroundHydrogen gas (H2), a novel and beneficial gaseous molecule, plays a significant role in plant growth and development processes. Hydrogen-rich water (HRW) is regarded as a safe and easily available way to study the physiological effects of H2 on plants. Several recent research has shown that HRW attenuates stress-induced seed germination inhibition; however, the underlying modes of HRW on seed germination remain obscure under non-stress condition.ResultsIn this current study, we investigated the possible roles of gibberellin (GA) and abscisic acid (ABA) in HRW-regulated seed germination in wax gourd (Benincasa hispida) through pharmacological, physiological, and transcriptome approaches. The results showed that HRW application at an optimal dose (50% HRW) significantly promoted seed germination and shortened the average germination time (AGT). Subsequent results suggested that 50% HRW treatment stimulated GA production by regulating GA biosynthesis genes (BhiGA3ox, BhiGA2ox, and BhiKAO), whereas it had no effect on the content of ABA and the expression of its biosynthesis (BhiNCED6) and catabolism genes (BhiCYP707A2) but decreased the expression of ABA receptor gene (BhiPYL). In addition, inhibition of GA production by paclobutrazol (PAC) could block the HRW-mediated germination. Treatment with ABA could hinder HRW-mediated seed germination and the ABA biosynthesis inhibitor sodium tungstate (ST) could recover the function of HRW. Furthermore, RNA-seq analysis revealed that, in the presence of GA or ABA, an abundance of genes involved in GA, ABA, and ethylene signal sensing and transduction might involve in HRW-regulated germination.ConclusionsThis study portrays insights into the mechanism of HRW-mediated seed germination, suggesting that HRW can regulate the balance between GA and ABA to mediate seed germination through ethylene signals in wax gourd.

Tracking the global anthropogenic gallium cycle during 2000–2020: A trade-linked multiregional material flow analysis

Byproduct metals are essential to global low carbon transition since they are irreplaceable in modern renewable energy technologies. Gallium (Ga) is classified as one critical byproduct metal due to its extensive use in electronic applications and low carbon technologies, as well as its limited resource endowment. It is urgent to uncover the global and regional Ga stocks and flows so that the potential supply risks can be mitigated. This study maps the global and regional Ga cycles for the period of 2000–2020 by employing a trade-linked multiregional material flow analysis (MFA) method. Our results show that 79% of the global Ga co-mined from bauxite ended up in red mud or entered the aluminum cycle as an impurity, indicating a significant recycling potential. Different involved regions have different but complementary roles in the global Ga supply chain. China dominates the global primary Ga production, accounting for 97% of the global total in 2020. Japan and the United States are key players in high-purity Ga refining and rely on Ga to support their electronic devices manufacturing. Unfortunately, Ga recycling practices are still not occurring due to the low Ga concentrations in major applications. Since the global demand for Ga will continue to grow in the near future, it is urgent to initiate collaborative efforts so that Ga recycling can be enhanced. These efforts are critical to ensure the sustainable Ga supply and facilitate the global transition toward low carbon development.

A tree peony RING-H2 finger protein, PsATL33, plays an essential role in cold-induced bud dormancy release by regulating gibberellin content.

Bud dormancy is crucial for woody perennial plants to resist low-temperature stress in winter. However, the molecular regulatory mechanisms underlying bud dormancy release are largely unclear. Here, a tree peony (Paeonia suffruticosa) transcript ARABIDOPSIS TOXICOS EN LEVADURA 33 (PsATL33), encoding a RING-H2 finger protein, was selected from previously generated RNA sequencing data of chilling-treated buds. The objective of this study is to investigate the role of PsATL33 in the regulation of cold-induced bud dormancy release. Subcellular localization assay revealed that PsATL33 was localized to the nucleus and plasma membrane. Reverse transcription-quantitative PCR analysis showed that PsATL33 was dramatically upregulated during cold-triggered bud dormancy release. Exogenous treatments with gibberellin (GA3) increased, but abscisic acid (ABA) inhibited the transcription of PsATL33. Ectopic transformation assay indicated that overexpression of PsATL33 in petunia promoted seed germination, plant growth, and axillary bud break. Silencing of PsATL33 in tree peony through virus-induced gene silencing assay delayed bud dormancy release. tobacco rattle virus (TRV)-PsATL33-infected buds exhibited reduced expression levels of dormancy break-related genes EARLY BUD-BREAK 1 (PsEBB1) and CARBOXYLESTERASE 15 (PsCXE15). Silencing of PsATL33 decreased the accumulation of bioactive GAs, GA1 and GA3, rather than ABA. Transcript levels of several genes involved in GA biosynthesis and signaling, including GA20-OXIDASE 1 (PsGA20ox1), GA3-OXIDASE 1 (PsGA3ox1), PsGA3ox3, GA2-OXIDASE 1 (PsGA2ox1), and GA-INSENSITIVE 1A (PsGAI1A), were changed by PsATL33 silencing. Taken together, our data suggest that PsATL33 functions as a positive regulator of cold-induced bud dormancy release by modulating GA production.

Studies of Impact on Bioactive Molecules of SB2 Isolate and their PGPR Activities from the Marine Environment

Marine microbes are important sources for recovering bioactive substances. One of the marine isolates, SB2, used a variety of media, with tryptic soy broth showing the best growth and yellow coloring. The largest amount of biomass was produced after 72 hours when the strain SB2 was cultured on glucose, molasses, and peptone, a yeast extract containing carbon and nitrogen sources. Yellow pigment must be extracted using methanol, and the isolate SB2 produced the most of this color. At a concentration of 100 g ml-1 of several bacterial pathogens, the recovered pigment from the SB2 isolate exhibited antibacterial action. The maximum production of IAA and GA is shown in TS broth, which is additionally augmented by the siderophore synthesis of catechol and salicylate. The SB2 also produces IAA and GA. In contrast, the highest level of ACC deaminase activity was found in nutrient broth. Due to the generation of pigment, the strain SB2 may be essential for Plant Growth Promoting Rhizobacteria (PGPR) and antibacterial properties.

Identification of Rhizosphere Endophytes and Evaluation of Their Impact on Growth of Chia (Salvia hispanica L.)

Endophytic microorganisms promote root growth, improve nutrient uptake efficiency and produce more yields. By collaborating with endophytic microorganisms, plants experience enhanced growth. This study was focused on endophytes from Chia plants in Bhukkapatna, Tumakur with the objective of molecular characterization of efficient endophytic microorganisms and its impact on growth of Chia. Twelve bacterial isolates were identified, with eight displaying nitrogen fixation, phosphate solubilisation, potassium fixation, production of IAA, GA, siderophore and exopolysaccharide production. Molecular characterization using 16S rRNA revealed their identities as Pseudomonas fluorescens, Bacillus cereus, Stenotrophomonas maltophilia, and Enterobacter cloacae. Among these, Enterobacter cloacae (CEPB8) exhibited highest positive impact on Chia plant growth. In greenhouse conditions, treatments involving combinations of all four demonstrated the highest plant height (35.467cm) and biomass (158.37 grams) at harvest, surpassing the control group. Combined treatments outperformed individual strains, highlighting synergy. The study affirms that endophytic microorganisms significantly enhanced growth in Chia plant.

Optimization of chemical conditions for metabolites production by Ganoderma lucidum using response surface methodology and investigation of antimicrobial as well as anticancer activities.

Ganoderma lucidum (G. lucidum) is a medicinal mushroom that is known for its ability to produce compounds with physiological effects on human health. This research was undertaken to amplify the production of bioactive components of G. lucidum under optimal cultivation conditions, obtained in a submerged state and utilized in solid state fermentation, with the purpose of enhancing antimicrobial and anticancer activities. The results indicated that titanium dioxide (TiO2 NPs), magnesium oxide nanoparticles (MgO2 NPs), and B6, along with glucose syrup and CLS syrups, were the most effective for producing GA, while wheat starch and whey protein, along with MgO2 NPs and B6 vitamin, stimulated polysaccharide production using the One Factor at a Time (OFAT) method. After screening, the response surface method (RSM) statistically indicated that the media containing 42.11 g/L wheat starch with 22 g/L whey protein and 50 g/L glucose syrup with 30 g/L CSL were found to be the best conditions for polysaccharide (21.47% of dry weight biomass) and GA (20.35 mg/g dry weight biomass) production, respectively. The moss of the fruit body of G. lucidum produced under optimal GA conditions had the highest diversity in flavonoids and phenolic acids and significant antimicrobial activity against Esherichia coli (E. coli) and Bacillus subtilis (B. subtilis). In addition, the IC50 levels of shell and stem of G. lucidum were 465.3 and 485.7 μg/mL, respectively, while the moss did not reach 50% inhibition. In the end, the statistical approaches utilized in this research to elevate the levels of bioactive components in the fruiting body of G. lucidum produced a promising natural source of antimicrobial and anticancer agents.

Enhancing productivity and profitability of linseed (Linum usitassimum L.) through foliar application of growth regulators

Considering the profitability, two foliar applications of auxin @ 2.0 ppm (one each at vegetative & flowering stage) was found to be the best treatment having additional net gain of Rs. 6226/ha over control with acceptable linseed seed yield of 1087 kg/ha under rainfed mid hill conditions of Himachal Pradesh. However, the treatments involving GA, applied either alone or in combination with auxin although have higher seed yield over the other treatments but could not achieve better returns due to higher cost of GA product adding to higher cost of cultivation.

Screening of Cadmium-Resistant Microbes to Improve the Tolerance of Sorghum bicolor (L.) Moench Against Cadmium

To improve the cadmium (Cd) resistance and the remediation ability of Sorghum bicolor (L.) Moench, fourteen Cd-resistant bacteria were screened from cadmium-contaminated soil, together with two strains preserved in the laboratory. It was found that 3 strains (ZR451, ZR452, and ZJSH1) significantly promoted the growth of Cd-stressed S. bicolor in hydroponics and mitigated Cd toxicity to plants, and SR8, ZRK1, and ZR211 promoted sorghum growth lightly. Further studies indicated that strains SR8, ZR211, and ZJSH1 were Cd-resistant and acid-resistant strains. Strains ZR211and ZR121 significantly produced two hormones (SA and GA), ZJSH1 significantly produced IAA and SA, and strains SR8, ZR451 and ZR452 produced one hormone. Strains SR8, ZR451, ZR452, and ZJSH1 produced siderophores. In addition, strain ZJSH1fixed nitrogen and produced ACC deaminase, while ZR451 and ZJSH1 solubilized phosphorus Correlation analysis showed that the Cd resistance of the strains was significantly and positively correlated with their IAA and GA production. The screening of the three cadmium resistant strains ZJSH1 (Sphingomonas paucimobilis), ZR451 (Bacillus cereus) and ZR452 (Bacillus cereus) provided bacterial resources for the efficient remediation of Cd-contaminated soils by bacterial - S. bicolor combination.

Light on perenniality: Para-dormancy is based on ABA-GA antagonism and endo-dormancy on the shutdown of GA biosynthesis.

Perennial para- and endo-dormancy are seasonally separate phenomena. Whereas para-dormancy is the suppression of axillary buds (AXBs) by a growing shoot, endo-dormancy is the short-day elicited arrest of terminal and AXBs. In hybrid aspen (Populus tremula x P. tremuloides) compromising the apex releases para-dormancy, whereas endo-dormancy requires chilling. ABA and GA are implicated in both phenomena. To untangle their roles, we blocked ABA biosynthesis with fluridone (FD), which significantly reduced ABA levels, downregulated GA-deactivation genes, upregulated the major GA3ox-biosynthetic genes, and initiated branching. Comprehensive GA-metabolite analyses suggested that FD treatment shifted GA production to the non-13-hydroxylation pathway, enhancing GA4 function. Applied ABA counteracted FD effects on GA metabolism and downregulated several GA3/4 -inducible α- and γ-clade 1,3-β-glucanases that hydrolyze callose at plasmodesmata (PD), thereby enhancing PD-callose accumulation. Remarkably, ABA-deficient plants repressed GA4 biosynthesis and established endo-dormancy like controls but showed increased stress sensitivity. Repression of GA4 biosynthesis involved short-day induced DNA methylation events within the GA3ox2 promoter. In conclusion, the results cast new light on the roles of ABA and GA in dormancy cycling. In para-dormancy, PD-callose turnover is antagonized by ABA, whereas in short-day conditions, lack of GA4 biosynthesis promotes callose deposition that is structurally persistent throughout endo-dormancy.

A petunia transcription factor, PhOBF1, regulates flower senescence by modulating gibberellin biosynthesis.

Flower senescence is commonly enhanced by the endogenous hormone ethylene and suppressed by the gibberellins (GAs) in plants. However, the detailed mechanisms for the antagonism of these hormones during flower senescence remain elusive. In this study, we characterized one up-regulated gene PhOBF1, belonging to the basic leucine zipper transcription factor family, in senescing petals of petunia (Petunia hybrida). Exogenous treatments with ethylene and GA3 provoked a dramatic increase in PhOBF1 transcripts. Compared with wild-type plants, PhOBF1-RNAi transgenic petunia plants exhibited shortened flower longevity, while overexpression of PhOBF1 resulted in delayed flower senescence. Transcript abundances of two senescence-related genes PhSAG12 and PhSAG29 were higher in PhOBF1-silenced plants but lower in PhOBF1-overexpressing plants. Silencing and overexpression of PhOBF1 affected expression levels of a few genes involved in the GA biosynthesis and signaling pathways, as well as accumulation levels of bioactive GAs GA1 and GA3. Application of GA3 restored the accelerated petal senescence to normal levels in PhOBF1-RNAi transgenic petunia lines, and reduced ethylene release and transcription of three ethylene biosynthetic genes PhACO1, PhACS1, and PhACS2. Moreover, PhOBF1 was observed to specifically bind to the PhGA20ox3 promoter containing a G-box motif. Transient silencing of PhGA20ox3 in petunia plants through tobacco rattle virus-based virus-induced gene silencing method led to accelerated corolla senescence. Our results suggest that PhOBF1 functions as a negative regulator of ethylene-mediated flower senescence by modulating the GA production.

Multi-strategy in production of high titer gluconic acid by the fermentation of concentrated cellulosic hydrolysate with Gluconobacter oxydans

Cellulosic hydrolysate from the hydrolysis of glucan-riched biomass can offer abundantly bioavailable glucose, which is an alternative feedstock for gluconic acid production. In order to speed up the process of cellulosic-based gluconic acid synthesis industrialization, cost reduction by using efficient substrate in batch-fermentation with high yield and productivity is extremely important. However, enriched glucose obtained by concentrating enzymatic hydrolysate inevitably ascends the viscosity, resulting in a lower oxygen transfer rate that cannot meet the requirement of bio-oxidation with Gluconobacter oxydans , resulting in gluconic acid productivity decreased drastically once the glucose content in the concentrated enzymatic hydrolysate was over 240 g/L with corresponding viscosity over 4 mPa·s. In view of the above problems, a combined strategy of activated carbon treatment and high-tension oxygen supply was applied to improve efficiency. Finally, approximately 230 g/L gluconic acid with 9.6 g/L/h productivity was achieved, which enabled the industrial-scale gluconic acid bio-production from cellulosic materials . • COS-SSB system can efficiently enhance the oxygen transfer rate and productivity. • CEH contain 240 g/L glucose could be used for GA production after AC treatment. • 231 g/L GA with 9.6 g/L/h productivity was achieved in CEH by combined strategy.

​Plant Growth Promoting Mesorhizobia as a Potential Inoculant for Chickpea (Cicer arietinum L.): A Review

Chickpea establish symbiotic relationship with Mesorhizobium ciceri and fixes atmospheric nitrogen, which depends on the efficacy of the Mesorhizobium strains, crop management, soil and environmental factors. A multi-trait Mesorhizobium isolate having more than one Plant growth promoting (PGP) traits often stimulates plant growth directly by IAA and GA production, enhances nutrient uptake by solubilizing phosphorus and siderophore production while indirect growth promotion is by prevention of some pathogenic microorganisms by producing HCN. Several studies revealed that plant growth attributes and yield was increased with inoculation of multi trait Rhizobium isolates. The occurrence of different PGP traits of Mesorhizobium and their effects on plant growth will be discussed in this review paper.

Augmented growth of Cd-stressed rice seedlings with the application of phytostimulating, root-colonizing, Cd-tolerant, leaf-endophytic fungi Colletotrichum spp. isolated from Eupatorium triplinerve

The potential of plant growth-promoting endophytic fungi (PGPEF) in mycoremediation has received notable attention in recent years. Unlike other root-colonizing microorganisms, PGPEF colonization under Cadmium (Cd) stress is a less-revealed phenomenon. Among eighteen fungal isolates from the leaves of Eupatorium triplinerve, twelve were found as the species of Colletotrichum and remaining six belong to Fusarium based on phenotypic characterization. However, only two PGPEF isolates (ALE15 and ALE18) were finally selected based on possession of ACCD activity (~0.84 and 0.47 nM/µg protein/h, respectively) and higher Cd tolerance (1000 and 750 µg/mL, respectively). Moreover, the said isolates showed IAA production (~248 and 289 µg/mL), GA production (~86 and 88 AUs), phosphate solubilization (~165 and 256 µg/mL, respectively) under Cd stress. ALE18 strain was found to produce siderophore too. Molecular identification through sequencing of ITS region of both isolates confirmed their identity as species of Colletotrichum. Furthermore, FESEM-EDAX and AAS analyses supported their Cd bioaccumulation ability in mycelial cells that directly impacted to assist rice seedlings’ (IR-36 cultivar) growth under Cd stress. Successful root colonization was also observed through FESEM and fluorescence microscopic studies. Finally, the detached leaf experiment with six economically important crops assured their applicability on field-scale as non-pathogenic PGPEF candidates.

A high-throughput visual screening method for p-hydroxybenzoate hydroxylase to increase phenolic compounds biosynthesis

BackgroundGallic acid (GA) and pyrogallol are phenolic hydroxyl compounds and have diverse biological activities. Microbial-based biosynthesis, as an ecofriendly method, has been used for GA and pyrogallol production. In GA and pyrogallol biosynthetic pathways, the low hydroxylation activity of p-hydroxybenzoate hydroxylase (PobA) towards 3,4-dihydroxybenzoic acid (3,4-DHBA) limited the high-level biosynthesis of GA and pyrogallol.ResultsThis work reported a high activity PobA mutant (Y385F/T294A/V349A PobA) towards 3,4-DHBA. This mutant was screened out from a PobA random mutagenesis library through a novel naked eye visual screening method. In vitro enzyme assay showed this mutant has a kcat/Km of 0.059 μM−1 s−1 towards 3,4-DHBA, which was 4.92-fold higher than the reported mutant (Y385F/T294A PobA). Molecular docking simulation provided the possible catalytic mechanism explanation of the high activity mutant. Expression of this mutant in E. coli BW25113 (Fʹ) can generate 840 ± 23 mg/L GA from 1000 mg/L 3,4-DHBA. After that, this mutant was assembled into a de novo GA biosynthetic pathway. Subsequently, this pathway was introduced into a 3,4-DHBA-producing strain (E. coli BW25113 (Fʹ)ΔaroE) to achieve 301 ± 15 mg/L GA production from simple carbon sources. Similarly, assembling this mutant into a de novo pyrogallol biosynthetic pathway enabled 129 ± 15 mg/L pyrogallol production.ConclusionsThis work established an efficient screening method and generated a high activity PobA mutant. Assembling this mutant into de novo GA and pyrogallol biosynthetic pathways achieved the production of these two compounds from glucose. Besides, this mutant has great potential for the production of GA or pyrogallol derivatives. The screening method could be used for other GA biosynthesis-related enzymes.

Production of the plant hormone gibberellin by rhizobia increases host legume nodule size.

Plant-associated microbes have evolved the ability to independently produce gibberellin (GA) phytohormones as a mechanism to influence their host. Indeed, GA was first discovered as a metabolite from the fungal rice pathogen Gibberella fujikuroi, which uses it as a virulence factor. Though some bacterial plant pathogens similarly use GA to promote infection, symbiotic nitrogen-fixing bacteria (rhizobia), which inhabit the root nodules of legumes, also can produce GA, suggesting a role in symbiosis. The bacterial GA biosynthetic operon has been identified, but in rhizobia this typically no longer encodes the final metabolic gene (cyp115), so that these symbionts can only produce the penultimate intermediate GA9. Here, we demonstrate that soybean (Glycine max) expresses functional GA 3-oxidases (GA3ox) within its nodules, which have the capability to convert GA9 produced by the enclosed rhizobial symbiont Bradyrhizobium diazoefficiens to bioactive GA4. This rhizobia-derived GA is demonstrated to cause an increase in nodule size and decrease in the number of nodules. The increase in individual nodule size correlates to greater numbers of bacterial progeny within a nodule, thereby providing a selective advantage to rhizobia that produce GA during the rhizobia-legume symbiosis. The expression of GA3ox in nodules and resultant nodulation effects of the GA product suggests that soybean has co-opted control of bioactive GA production, and thus nodule size, for its own benefit. Thus, our results suggest rhizobial GA biosynthesis has coevolved with host plant metabolism for cooperative production of a phytohormone that influences nodulation in a mutually beneficial manner.

Potentials of Lactic Acid Bacteria in Enhancing Nodulation of Bradyrhizobium daqingense and Yield in Soybean

Background: The ferments of lactic acid bacteria (LAB) are used since decades in agricultural practice to control diseases, to promote plant growth and also to improve soils. However the functional roles of LAB in phytomicrobiome need to be discovered, which would result in understanding of the symbiotic relationship between LAB and plants and that could be exploited to improve agricultural production. Methods: In this study, the scientific investigation was carried out for pot culture evaluation of six efficient LAB isolates from soybean rhizosphere, on nodulation and yield of soybean in green house condition, which were proven positive for IAA and GA production and PGPR traits. Result: Among the eight different treatment combination with Bradyrhizobium daqingense the treatment which received consortium of all six LAB isolates had significant impact on plant growth characters viz. plant height, root length, number of branches and chlorophyll content at 30 and 60 DAS. The LAB consortia also showed significantly high nodule number (47.67), nodule dry weight (117 mg plant-1) and leg haemoglobin content (6.27 mg g-1 fresh nodule) at 30 DAS. The yield and yield related traits was also highest in consortium treated plants. The property of plant to produce more nodules and healthy root growth can be attributed to IAA producing ability of inoculated LAB isolates.

Heterologous expression of membrane-bound alcohol dehydrogenase-encoding genes for glyceric acid production using Gluconobacter sp. CHM43 and its derivatives.

In contrast to D-glyceric acid (D-GA) production with 99% enantiomeric excess (ee) by Acetobacter tropicalis NBRC 16470, Gluconobacter sp. CHM43 produced 19.6g L-1 of D-GA with 73.7% ee over 4days of incubation in flask culture. To investigate the reason for this enantiomeric composition of GA, the genes encoding membrane-bound alcohol dehydrogenase (mADH) of A. tropicalis NBRC 16470, composed of three subunits (adhA, adhB, and adhS), were cloned using the broad-host-range vector pBBR1MCS-2 and heterologously expressed in Gluconobacter sp. CHM43 and its ΔadhAB ΔsldBA derivative TORI4. Reverse-transcription quantitative real-time polymerase chain reaction demonstrated that adhABS genes from A. tropicalis were expressed in TORI4 transformants, and their membrane fraction exhibited mADH activities of 0.13 and 0.31 U/mg with or without AdhS, respectively. Compared with the GA production of TORI4-harboring pBBR1MCS-2 (1.23g L-1), TORI4 transformants expressing adhABS and adhAB showed elevated GA production of 2.46 and 3.67g L-1, respectively, suggesting a negative effect of adhS gene expression on GA production as well as mADH activity in TORI4. Although TORI4 was found to produce primarily L-GA with 42.5% ee, TORI4 transformants expressing adhABS and adhAB produced D-GA with 27.6% and 49.0% ee, respectively, demonstrating that mADH of A. tropicalis causes a sharp increase in the enantiomeric composition of D-GA. These results suggest that one reason for D-GA production with 73.7% ee in Gluconobacter spp. might be a property of the host, which possibly produces L-GA intracellularly. KEY POINTS: • Membrane-bound ADH from Acetobacter tropicalis showed activity in Gluconobacter sp. • D-GA production from glycerol was performed using recombinant Gluconobacter sp. • Enantiomeric excess of D-GA was affected by both membrane and intracellular ADHs.