Morphological responses of different eucalypt clones submitted to glyphosate drift

This work aimed to evaluate the effects of simulated glyphosate drift on leaf growth and micromorphology of Eucalyptus spp. clones, using subdoses. A factorial scheme consisting of three clones, Eucalyptus urophylla, E. grandis and the hybrid E. urophylla × E. grandis (E. urograndis) and five sub-rates (0; 43.2; 86.4; 172.8 and 345.6 g e.a. ha⁻¹ of glyphosate) were used in a randomized block design, with four repetitions. The herbicide was applied on the plants so as not to reach the superior third, 23 days after seedling planting. At 7 and 15 days after application (DAA), the leaves collected from the first basal branch of the plants were processed according to the conventional methodology used for micromorphological studies. The effects of glyphosate drift were proportional to the rates tested, with E. urophylla being more tolerant to the herbicide than E. grandis and E. urograndis. Glyphosate symptoms were the same for the different clones tested, being characterized by wilting, chlorosis and leaf curling, and, at higher rates, by necrosis, foliar senescence and death of the eucalypt plants. Plants submitted to 172.8 and 345.6 g ha⁻¹ of glyphosate had severe injuries in the aerial part, affecting their development, resulting in reduced height, stem diameter and dry mass at 50 DAA. The micromorphological damages occurred prior to the appearance of visible symptoms, with erosion of the epicuticular waxes and fungal hypha infestation in plants exposed to glyphosate drift being observed in the three clones. No marked difference in leaf micromorphology was observed that could explain the differential tolerance among the three clones studied. The results show that further studies on wax and cuticle constitution of Eucalyptus spp. are needed for the elucidation of the mechanisms of differential tolerance of eucalypt species and clones to glyphosate.     

Characterization and efficacy of Muscodor cinnamomi in promoting plant growth and controlling Rhizoctonia root rot in tomatoes

Muscodor cinnamomi was selected and investigated for its in vitro ability to produce indole-3-acetic acid (IAA) to solubilize different toxic metal (Ca, Co, Cd, Cu, Pb, Zn)-containing insoluble minerals and tolerance to metals, herbicides and an insecticide. The results indicated that this fungus is able to produce IAA (45.36 ± 2.40 μg ml⁻¹) in liquid media. This phytohormone stimulated coleoptile elongation, and increased seed germination and root elongation of tested plants. The metal tolerance and solubilizing ability depended on the type of insoluble minerals. M. cinnamomi showed the highest growth tolerance on Ca-containing media at 150 mM, followed by Zn-containing media at 100 mM and Cd-containing media at 10 mM. This fungus tolerated the three herbicides (2,4-d-dimethylammonium, glyphosate and paraquat dichloride) and an insecticide (methomyl) at the recommended dosages for field application. Moreover, M. cinnamomi completely controlled Rhizoctonia solani AG-2 root rot in tomato plants, and increased root length, shoot dry weight and root dry weight. This is the first report of in vitro IAA production, solubilization of insoluble metal minerals, and tolerance to herbicides, an insecticide and metals as well as the plant growth promoting ability of M. cinnamomi.     

Characterization and site-directed mutagenesis of a novel class II 5-enopyruvylshikimate-3-phosphate (EPSP) synthase from the deep-sea bacterium Alcanivorax sp. L27

The 5-enolpyruvylshikimate-3-phosphate synthase (EPSPS) is a key enzyme in the aromatic amino acid biosynthetic pathway in microorganisms and plants, which catalyzes the formation of 5-enolpyruvylshikimate-3-phosphate (EPSP) from shikimate-3-phosphate (S3P) and phosphoenolpyruvate (PEP). In this study, a novel AroA-encoding gene was identified from the deep sea bacterium Alcanivorax sp. L27 through screening the genomic library and termed as AroA_A.sp. A phylogenetic analysis revealed that AroA_A.sp (1317 bp and 438 amino acids) is a class II AroA. This enzyme exhibited considerable activity between pH 5.5 and pH 8.0 and notable activity at low temperatures. The K_M for PEP and IC₅₀ [glyphosate] values (the concentration of glyphosate that inhibited enzyme activity by 50%) of AroA_A.sp were 78 μM and 1.5 mM, respectively. Furthermore, site-directed mutagenesis revealed that the G100A mutant had a 30-fold increase in the IC₅₀ [glyphosate] value; while the L105P mutant showed only 20% catalytic activity compared to wild-type AroA_A.sp. The specific activity of the wild-type AroA_A.sp, the G100A mutant and the L105P mutant were 7.78 U/mg, 7.26 U/mg and 1.76 U/mg, respectively. This is the first report showing that the G100A mutant of AroA displays considerably improved glyphosate resistance and demonstrates that Leu105 is essential for the enzyme's activity.     

Thermolabile antifreeze protein produced in Escherichia coli for structural analysis

Inclusion bodies of recombinant human growth hormone (r-hGH) were isolated from Escherichia coli, enriched and solubilized in 100 mM Tris buffer containing 6 M n-propanol and 2 M urea. Around 4 mg/ml of r-hGH from inclusion bodies were solubilized in 6 M n-propanol-based buffer containing 2 M urea. Existence of native-like secondary structure of r-hGH in 6 M n-propanol solution was confirmed by CD and fluorescence spectra. Solubilized r-hGH was subsequently refolded by pulsatile dilution, purified to homogeneity and found to be functionally active. Tris buffer containing 6 M n-propanol and 2 M urea also effectively solubilized a number of proteins expressed as inclusion bodies in E. coli. Mild solubilization of inclusion body proteins, chaotropic effect of n-propanol at high concentration and kosmotropic effect at lower concentration helped in improved refolding of the solubilized protein. Around 40% of the r-hGH in the form of inclusion body aggregates was refolded into bioactive form while using n-propanol as solubilization agent. Solubilization with 6 M n-propanol solution thus can be a viable alternative for achieving high throughput recovery of bioactive protein from inclusion bodies of E. coli.     

Anthraquinone-based bird repellent for sunflower crops

Non-lethal alternatives are needed to manage bird damage to confectionery and oilseed sunflower crops (Helianthus annuus). Ring-necked pheasants (Phasianus colchicus) can cause localized damage to newly planted sunflower, and blackbirds (Icterids) damage ripening sunflower annually in the United States of America. We conducted seed germination experiments, a repellent efficacy study with ring-necked pheasants and Avipel^® repellent (a.i. 50% 9,10-anthraquinone), and laboratory and field efficacy studies with common grackles (Quiscalus quiscula) and Avipel^®-treated confectionery sunflower. Compared to the germination of seeds not treated with anthraquinone, we observed no negative effects of up to 12,223 ppm, 14,104 ppm, and 11,569 ppm anthraquinone seed treatments for germination of confectionery sunflower, oilseed sunflower, and canola seeds, respectively. Pheasants avoided emergent sunflower seedlings (12 days post-planting) from 15,800 ppm anthraquinone seed treatments during a caged preference test (P = 0.045). We observed a positive concentration–response relationship (P = 0.001) and predicted a threshold concentration (i.e., 80% repellency) of 9200 ppm anthraquinone for common grackles offered Avipel^®-treated confectionery sunflower seeds. Grackles also reliably discriminated between untreated sunflower and seeds treated with 1300 ppm anthraquinone in captivity (P < 0.001). During our field efficacy study for ripening confectionery sunflower, we observed 18% damage among anthraquinone-treated enclosures and 64% damage among untreated enclosures populated with common grackles (P < 0.001). Harvested seed mass averaged 2.54 kg (dry weight) among treated enclosures and 1.24 kg among untreated enclosures (P < 0.001). Our laboratory and field efficacy data provide a reliable basis for planning future field applications of anthraquinone-based repellents for protection of sunflower crops. Supplemental field efficacy studies are necessary for development of an effective avian repellent and management of avian depredation of ripening agricultural crops, including oilseed sunflower.     

The interaction of two potential fungal bioherbicides and a sub-lethal rate of glyphosate for the control of shattercane

Greenhouse and laboratory experiments were conducted with the potential bioherbicides Colletotrichum graminicola (Cg) and Gloeocercospora sorghi (Gs) for control of shattercane weed. Single-spray tank mixture applications containing different ratios of the two fungi resulted in additive percent weed biomass losses. Intraspecific (Cg + Cg or Gs + Gs) and interspecific (Cg + Gs or Gs + Cg) sequential applications 1- or 7-days apart indicated antagonistic interactions in percent biomass loss. Application of either fungus with, or 1–3 days prior to, a sub-lethal concentration of glyphosate resulted in an antagonistic percent biomass loss; while application of glyphosate prior to either potential bioherbicide resulted in a synergistic weed disease response. Conidia germination studies conducted both in vitro on agar plates and with leaf impression peels suggest that antagonistic interactions observed in weed disease severity are probably due to the host–pathogen response following infection.     

Comprehensive genomics and expression analysis of eceriferum (CER) genes in sunflower (Helianthus annuus)

Sunflower occupies the fourth position among oilseed crops the around the world. Eceriferum (CER) is an important gene family that plays critical role in very-long-chain fatty acids elongation and biosynthesis of epicuticular waxes under both biotic and abiotic stress conditions. The aim of present study was to investigate the effect of sunflower CER genes during drought stress condition. Thus, comparative analysis was undertaken for sunflower CER genes with Arabidopsis genome to determine phylogenetic relationship, chromosomal mapping, gene structures, gene ontology and conserved motifs. Furthermore, we subjected the sunflower cultivars under drought stress and used qRT-PCR analysis to explore the expression pattern of CER genes during drought conditions. We identified thirty-seven unevenly distributed CER genes in the sunflower genome. The phylogenetic analysis revealed that CER genes were grouped into seven clades in Arabidopsis, Helianthus annuus, and Gossypium hirsutum. Expression analysis showed that genes CER10 and CER60 were upregulated in sunflower during drought conditions, indicating that these genes are activated during drought stress. The results obtained will serve to characterize the CER gene family in sunflower and exploit the role of these genes in wax biosynthesis under limited water conditions.Key messageCuticular waxes protect the plants from drought stress, so we observed the expression of wax bio synthesis genes in recently sequences genome of Helianthus annuus. We observed that expression of wax biosynthesis genes CER10 and CER60 was upregulated when the plants were subjected to drought stress.     

Effect of salt on survival and P-solubilization potential of phosphate solubilizing microorganisms from salt affected soils

A total of 23 phosphate solubilizing bacteria (PSB) and 35 phosphate solubilizing fungi (PSF) were isolated from 19 samples of salt affected soils. The ability of 12 selected PSB and PSF to grow and solubilize tricalcium phosphate in the presence of different concentrations of NaCl was examined. Among 12 PSB, Aerococcus sp. strain PSBCRG₁-1 recorded the highest (12.15) log viable cell count at 0.4 M NaCl concentration after 7 days after incubation (DAI) and the lowest log cell count (1.39) was recorded by Pseudomonas aeruginosa strain PSBI₃-1 at 2.0 M NaCl concentration after 24 h of incubation. Highest mycelial dry weight irrespective of NaCl concentrations was recorded by the Aspergillus terreus strain PSFCRG₂-1 (0.567 g). The percent P_i release, in general, was found to increase with increase in NaCl concentration up to 0.8 M for bacterial solubilization and declined thereafter. At 15 DAI, strain Aerococcus sp. strain PSBCRG₁-1 irrespective of NaCl concentrations showed the maximum P-solubilization (12.12%) which was significantly superior over all other isolates. The amount of P_i released in general among PSF was found to decrease with increase in NaCl concentration at all the incubation periods. Aspergillus sp. strain PSFNRH-2 (20.81%) recorded the maximum P_i release irrespective of the NaCl concentrations and was significantly superior over all other PSF at 7 DAI.     

Prospects of in vivo 31P NMR method in glyphosate degradation studies in whole cell system

The degradation of the phosphonate herbicide glyphosate (N-phosphonomethylglycine) by four taxonomically distinct microorganisms was studied in vivo in whole cell system using phosphorus nuclear magnetic spectroscopy (³¹P NMR). The time-course of glyphosate metabolization in dense cell cultures was followed by means of ³¹P NMR up to 21 days after the addition. The results obtained by this non-invasive way confirmed that the cells of Spirulina platensis and Streptomyces lusitanus biodegrade herbicide. Moreover, phosphorus starvation influenced the rate of glyphosate degradation by S. platensis. On the other hand, the results of similar measurements in the cultures of green algae Chlorella vulgaris showed that this aquatic plant, however growing in the medium containing 1 mM of N-phosphonomethylglycine, did not seem to posses the ability of its biodegradation. Additionally, the use of this method allowed us to find the new fungal strain Fusarium dimerum, which is able to biodegrade and utilize the glyphosate as the sole source of phosphorus. The results of our studies on usefulness of in vivo ³¹P NMR for tracing glyphosate degradation in whole cell systems revealed that this non-invasive, one-step method, might be considered as a valuable tool in environmental biotechnology of organophosphonate xenobiotics.     

Herbivory,mowing, and herbicides differently affect production and nutrient allocation of Alternanthera philoxeroides

This glasshouse study examined the effect of three damage types on plant growth and nutrient allocation of the invasive aquatic plant, alligator weed (Alternanthera philoxeroides). The damage included: repeated leaf removal, a single application of herbicide, and one-time shoot removal. Damage types were meant to simulate the effects of insect herbivory, chemical, and mowing/grazing, respectively. Response variables included plant biomass and both the concentration and abundance of nutrients. Complete shoot removal and herbicide treatments caused an initial decline in growth rate, followed by several weeks of increasing rates and finally a second decline during the fourth week. Plants from control and repeated leaf removal treatments showed a steady increase in growth rate from the treatment application to the final harvest, but control plants were accumulating biomass three times faster than repeated defoliation plants by the fifth week (9.7 and 3.5 g week⁻¹, respectively). Not surprisingly, all treatments led to lower total cumulative biomass 5 weeks after treatment application (mean 30.8 g) when compared with controls (49.0 g). However, despite the repeated leaf removal and complete shoot removal treatments removing similar quantities of biomass (mean 8.0 and 7.5 g respectively), repeated removal of leaves produced less total biomass (26.2 g) and led to less cumulative above ground biomass (20.1 g) than the other treatments (mean total = 33.1 g, mean above ground = 25.7 g). Repeated leaf removal also produced less below ground biomass (6.1 g) than the shoot removal treatment (8.5 g) and had the greatest negative effect on nitrogen and potassium abundance in plant tissues after 5 weeks. In addition, it reduced the amount of phosphorous to a lower level than herbicide treated or control plants. These results indicate that repeated leaf removal was the treatment most effective in reducing biomass and depleting nutrients in A. philoxeroides plants.     

Characterization and directed evolution of BliGO,a novel glycine oxidase from Bacillus licheniformis

Glycine oxidase (GO) has great potential for use in biosensors, industrial catalysis and agricultural biotechnology. In this study, a novel GO (BliGO) from a marine bacteria Bacillus licheniformis was cloned and characterized. BliGO showed 62% similarity to the well-studied GO from Bacillus subtilis. The optimal activity of BliGO was observed at pH 8.5 and 40 °C. Interestingly, BliGO retained 60% of the maximum activity at 0 °C, suggesting it is a cold-adapted enzyme. The kinetic parameters on glyphosate (K_m, k_cat and k_cat/K_m) of BliGO were 11.22 mM, 0.08 s⁻¹, and 0.01 mM⁻¹ s⁻¹, respectively. To improve the catalytic activity to glyphosate, the BliGO was engineered by directed evolution. With error-prone PCR and two rounds of DNA shuffling, the most evolved mutant SCF-4 was obtained from 45,000 colonies, which showed 7.1- and 8-fold increase of affinity (1.58 mM) and catalytic efficiency (0.08 mM⁻¹ s⁻¹) to glyphosate, respectively. In contrast, its activity to glycine (the natural substrate of GO) decreased by 113-fold. Structure modeling and site-directed mutation study indicated that Ser51 in SCF-4 involved in the binding of enzyme with glyphosate and played a crucial role in the improvement of catalytic efficiency.     

Biodegradation of the herbicide diuron by streptomycetes isolated from soil

The diuron degrading activity of 17 streptomycete strains, obtained from agricultural and non-agricultural soils, was determined in the laboratory. All strains were identified as Streptomyces sp. by phenotypic characteristics and PCR-based assays. The strains were cultivated in liquid medium with diuron (4 mg L⁻¹) at 25 °C for 15 days. Biodegradation activity was determined by high-performance liquid chromatography. The results indicated that all strains were able to degrade diuron, but to different amounts. Twelve strains degraded the herbicide by up to 50% and four of them by up to 70%. Strain A7-9, belonging to S. albidoflavus cluster, was the most efficient organism in the degradation of diuron, achieving 95% degradation after five days of incubation and no herbicide remained after 10 days. Overall, the strains isolated from agricultural soils exhibited higher degradation percentages and rates than those isolated from non-agricultural soils. Given the high degradation activity observed here, the streptomycete strains show a good potential for bioremediation of soils contaminated with diuron.     

Antibacterial activity of selected medicinal plants of northwest Pakistan traditionally used against mastitis in livestock

The present study aimed to investigate the efficacy of traditionally used anti-mastitis plants (Allium sativum, Bunium persicum, Oryza sativa and Triticum aestivum) in northwest Pakistan against bacterial pathogens. Selected plants were phytochemically screened for Alkaloids, Flavonoids, and Saponins and checked for in vitro antibacterial activity at concentration of 50 mg/ml against S. aureus, E. coli and K. pneumoniae by agar well diffusion method. Minimum inhibitory concentration and minimum bactericidal concentration was determined against multidrug resistant bacteria using tube dilution method. All extracts were found to significantly inhibit (p < 0.01, p < 0.05) the activity against bacterial strains examined. Among phytochemicals, alkaloids of all tested antimastitis plants produced significantly higher inhibition zones against bacteria. The minimum inhibitory concentration and minimum bactericidal concentration of phytochemicals and crude methanolic extracts against tested bacterial strains ranged between 12.5–50 mg/ml and 25–50 mg/ml, respectively. Medicinal plants traditionally used against mastitis are therapeutically active against bacterial pathogens. A. sativum and B. persicum were found to be potential candidate species for the development of novel veterinary drugs with low cost and fewer side effects.     

Factors influencing the return of submerged plants to a clear-water,shallow temperate lake

Lack of submerged vegetation was studied in a small, shallow, alkaline, clear-water lake with high nitrate concentration (mean 9 mg NO₃–N L⁻¹) and profuse filamentous green algae (FGA) (mainly Spirogyra sp.). A laboratory microcosm and two lake enclosure experiments were carried out using Elodea nuttallii (Planchon) St John. E. nuttallii grew about 1.7 times as well in sediment from its place of origin compared with sediment from the lake. Differential water quality had no effect, and neither sediment nor water prevented growth in the lake. Nutrient addition reduced plant growth by more than 55% because of shading from epiphytic filamentous green algae (shoot dry weight versus epiphytic algal dry weight, r = −0.491, P < 0.05). Transplanted Elodea plants grew better in enclosures in the lake than in laboratory conditions with lake water and sediment (P < 0.001, t-test). Rare Elodea individuals in the lake indicate the presence of plant propagules in the lake sediment, but excessive growth of filamentous green algae (summer mean 3.2 g dry weight m⁻²) significantly hamperd plant growth (shoot length reduced from 29 ± S.E.M. 1 to 25 ± 1 cm) and bird herbivory significantly reduced survival (from 82 ± 7 to 40 ± 6%) and shoot growth (from 78 ± 6 to 18 ± 5 cm) and thus eliminates establishment of even modest plant beds. Fish disturbance and sediment stability were not important. Restoration of submerged plants may require reduction of nitrate input, control of filamentous green algae and protection from birds.     

Antimalarial and antitubercular C-glycosylated benz[α]anthraquinones from the marine-derived Streptomyces sp. BCC45596

Three naturally new C-glycosylated benz[α]anthraquinone derivatives, urdamycinone E (1), urdamycinone G (2), dehydroxyaquayamycin (3) have been isolated from the marine Streptomycetes sp. BCC45596. Urdamycin E (4), the possible biosynthetic precursor of 1–3, has also been identified after a re-cultivation of the strain. These compounds (1–4) exhibited potent anti-Plasmodium palcifarum K1 strain with IC₅₀ values in a range of 0.0534–2.93 μg/mL and anti-Mycobacterium tuberculosis with minimum inhibition concentrations (MICs) in a range of 3.13–12.50 μg/mL. Cytotoxicity against KB, MCF-7, NCI-H187, and Vero cells was also evaluated.     

Biotransformation pathways of ginsenoside Rb1 to compound K by β-glucosidases in fungus Paecilomyces Bainier sp. 229

Ginsenoside Rb1 is the most abundant ginsenoside in Panax (ginseng). The hydrolysis of this ginsenoside produces compound K, the biologically active ginsenoside of ginseng. We previously identified a fungus Paecilomyces Bainier sp. 229 (sp. 229), which can efficiently convert ginsenoside Rb1 to compound K. In this report, the ginsenoside hydrolyzing β-glucosidases were isolated from sp. 229 and the pathway of the biotransformation of ginsenoside Rb1 to compound K by sp. 229 was investigated. Based on reverse-phase HPLC and TLC analysis, we found the main metabolic pathway is as follows: ginsenoside Rb1 → ginsenoside Rd → ginsenoside F2 → compound K. Moreover, the results showed that there were other metabolic pathways: ginsenoside Rb1 → ginsenoside XVII → ginsenoside F2 → compound K and ginsenoside Rb1 → ginsenoside Rg3 → ginsenoside Rh2. These processes would allow the specific bioconversion of ginsenoside Rb1 to various ginsenosides using an appropriate combination of specific microbial enzymes.     

Kocuria uropygioeca sp. nov. and Kocuria uropygialis sp. nov., isolated from the preen glands of Great Spotted Woodpeckers (Dendrocopos major)

Two new species of Gram-positive cocci were isolated from the uropygial glands of wild woodpeckers (Dendrocopos major) originating from different locations in Germany. A polyphasic approach confirmed the affiliation of the isolates to the genus Kocuria. Phylogenetic analysis based on the 16S rRNA gene showed high degree of similarity to Kocuria koreensis DSM 23367^T (99.0% for both isolates). However, low ANIb values of <80% unequivocally separated the new species from K. koreensis. This finding was further corroborated by DNA fingerprinting and analysis of polar lipid profiles. Furthermore, growth characteristics, biochemical tests, MALDI-TOF MS analysis, and G + C contents clearly differentiated the isolates from their known relatives. Besides, the woodpecker isolates significantly differed from each other in their whole-cell protein profiles, DNA fingerprints, and ANIb values. In conclusion, the isolated microorganisms constitute members of two new species, for which the names Kocuria uropygioeca sp. nov. and Kocuria uropygialis sp. nov. are proposed. The type strains are 36^T (DSM 101740^T = LMG 29265^T) and 257^T (=DSM 101741^T = LMG 29266^T) for K. uropygialis sp. nov. and K. uropygioeca sp. nov., respectively.     

Accumulation of radioiodine from aqueous solution by hydroponically cultivated sunflower (Helianthus annuus L.)

The suitability of sunflower plants (Helianthus annuus L.) for the phytoremediation of soils and waters contaminated with radioactive iodine was tested following the ¹²⁵I uptake from a hydroponic medium and translocation during 32-day cultivation. The plants accumulated about 26% of the applied activity in case of combination of ¹²⁵I (1.3 MBq) and 0.1 mM K¹²⁷I (“carrier ¹²⁵I”) and 47% when only ¹²⁵I (1.3 MBq, “non-carrier ¹²⁵I”) was added. When hydroponic medium was changed for the fresh one every 4 days, the plants accumulated up to 59% of starting activity of non-carrier ¹²⁵I. The ¹²⁵I distribution within the plant was followed using autoradiography. At low iodine level (non-carrier ¹²⁵I) the radionuclide was localized mainly in the roots. At high iodine concentrations (carrier ¹²⁵I) it was found mainly in the upper part of sunflower plants. All iodine removed from the liquid medium was found in the plant body. Volatilization of iodine (in the form of I⁰ or volatile organic compounds) apparently did not occur during accumulation and translocation. The achieved results indicate that sunflower can be used for phytoremediation of radioactive iodine, even if it is not its hyperaccumulator.     

Impact of rock materials and biofertilizations on P and K availability for maize (Zea Maize) under calcareous soil conditions

The present work evaluated the synergistic effects of soil fertilization with rock P and K materials and co-inoculation with P and K-dissolving bacteria [PDB (Bacillus megaterium var. phosphaticum) and KDB (Bacillus mucilaginosus and B. subtilis)] on the improvement of P and K uptake, P and K availability and growth of maize plant grown under limited P and K soil conditions (calcareous soil). The experiment was establishment with eight treatments: without rock P and K materials or bacteria inoculation (control), rock P (RP), rock K (RK), RP + PDB, RK + KDB and R(P + K)+(P + K)DB. Under the same conditions of this study, co-inoculation of PDB and KDB in conjunction with direct application of rock P and K materials (R(P + K)) into the soil increased P and K availability and uptake, and the plant growth (shoot and root growth) of maize plants grown on P and K limited soils.