Effects of Foliar Sprays of Phosphates on Powdery Mildew (Sphaerotheca pannosa) of Roses

Powdery mildew on plants of a local clone of Rosa indica Major was significantly controlled by a single spray of 25 mM aqueous solutions of K₂HPO₄, KH₂PO₄ plus KOH, or NaHCO₃, all plus Tween 20 (0.5 ml/l) or bupirimate (Nimrod) at 0.5 ml/l, which was applied 4 days before inoculation with conidial suspension of Sphaerotheca pannosa var. rosae. Disease incidence was reduced by 79, 71, 54 and 50%, as compared to controls on plants sprayed with KH₂PO₄ plus KOH, K₂HPO₄, NaHCO₃ or bupirimate, respectively. Phosphates were suppressive and expressed by disappearance of 99% of the pustules and conidia, as early as 2 days after a single spray on mildewed foliage. This treatment was efficient for at least 9 days after the first application when large infected greenhouse-grown plants were used. Re-application of these salts on the same plants reduced the lesion area by about 90% from that recorded before the application. Phosphate and bicarbonate were more suppressive than the systemic fungicide bupirimate in the early period (up to 2 days). The suppresion effects of bicarbonate and bupirimate, however, were short-term and not persistent, while the phosphate treatments remained significantly suppressive for up to 23 days, when the experiment was terminated. The inhibitory and suppressive effectiveness of phosphate salts is discussed in the light of their possible acceptance as ideal foliar fertilizers which should be considered for use in the field for disease control.     

Solubility of phosphorus added to four Manitoba soils with different calcium and magnesium contents

Summary The solubility of phosphorus was found to approximate that of dicalcium phosphate dihydrate and/or dimagnesium phosphate trihydrate when KH₂-PO₄, H₃PO₄ and K₂HPO₄ were added to four Manitoba soils. Eighty to one hundred, seventy to ninety and sixty to eighty per cent of the phosphorus added remained in solution when H₃PO₄, KH₂PO₄ and K₂HPO₄ were added, respectively. The solubility of the added phosphorus was high in all samples and relatively soluble compounds, dicalcium phosphate dihydrate and dimagnesium phosphate trihydrate, were most likely formed in the samples indicating that phosphorus added to these soils would be readily available to plants. Associate Professor and Professor respectively.     

Efficacy of Foliar Application of Phosphates in Controlling Powdery Mildew Fungus on Field-Grown Winegrapes: Effects on Cluster Yield and Peroxidase Activity in Berries

Seven foliar applications of 0.025M K₂HPO₄ and KH₂PO₄ (both plus Tween 20) and the commercial systemic fungicides, Dorado (Pyrifenox) 480 EC, Penconazole EC and Benomyl, were applied at 14-day intervals starting at 10-cm shoot length on field-grown Chardonnay winegrapes. Both phosphates and systemic fungicides inhibited development of powdery mildew fungus (Uncinula necator, Schw., Burr.) on fruit clusters, as compared with untreated control vines. Diseases, everity on clusters of plants treated with K₂HPO₄ and fungicides was 0.3 and 0.2, respectively, as compared with 1.3 on control clusters (on a 0–4 scale), for the first rating, conducted 10 days after the fifth application of fungicides and phosphates, Five days after the last application, disease severity was 3.5 on non-treated control clusters and 0.3 and 0.8 on clusters treated with Dorado and K₂HPO₄, respectively. Powdery mildew infection remarkably reduced the weight of non-treated control clusters as compared with Dorado and phosphate treated clusters. Phosphate treatment caused an increase (3-fold) of peroxidase activity in the soluble fraction of non-infected control berries. A remarkable peroxidase enhancement was detected in the soluble (8-fold) and ionically bound (2-fold) fractions from the phosphate-treated and infected berries. Results indicate that phosphates can be used as foliar fertilizers for disease control in the field and that peroxidase might, be involved in the defense process.     

Formation of Psicose from Glucose in Autoclaved and Uninoculated Fermentation Media

When a fermentation medium consisting of the high concentration of K₂HPO₄ and KH₂PO₄ and glucose as a sole carbon source is autoclaved in the alkaline side, an unknown sugar is formed. This sugar is identified as psicose by paper chromatography and high-voltage paper electrophoresis. The notion that weak alkali causes the isomerization of reducing sugar could account for the formation of psicose in the medium. It is thus concluded that psicose is chemically formed from glucose in the alkaline side and in the high concentration of K₂HPO₄ and KH₂PO₄ during autoclaving.     

Interference of some aqueous two-phase system phase-forming components in protein determination by the Bradford method

The interference of some specific aqueous two-phase system (ATPS) phase-forming components in bovine serum albumin (BSA) determination by the Bradford method was investigated. For this purpose, calibration curves were obtained for BSA in the presence of different concentrations of salts and polymers. A total of 19 salts [Na₂SO₄, (NH₄)₂SO₄, MgSO₄, LiSO₄, Na₂HPO₄, sodium phosphate buffer (pH 7.0), NaH₂PO₄, K₂HPO₄, potassium phosphate buffer (pH 7.0), KH₂PO₄, C₆H₈O₇, Na₃C₆H₅O₇, KCHO₂, NaCHO₂, NaCO₃, NaHCO₃, C₂H₄O₂, sodium acetate buffer (pH 4.5), and NaC₂H₃O₂] and 7 polymers [PEG 4000, PEG 8000, PEG 20000, UCON 3900, Ficoll 70000, PES 100000, and PVP 40000] were tested, and each calibration curve was compared with the one obtained for BSA in water. Some concentrations of salts and polymers had considerable effect in the BSA calibration curve. Carbonate salts were responsible for the highest salt interference, whereas citric and acetic acids did not produce interference even in the maximum concentration level tested (5 wt%). Among the polymers, UCON gave the highest interference, whereas Ficoll did not produce interference when used in concentrations up to 10 wt%. It was concluded that a convenient dilution of the samples prior to the protein quantification is needed to ensure no significant interference from ATPS phase-forming constituents.     

Optimization of chitinase production by a new <Emphasis Type="Italic">Streptomyces griseorubens</Emphasis> C9 isolate using response surface methodology

The purpose of this article is to use statistical Plackett–Burman and Box–Wilson response surface methodology to optimize the medium components and, thus, improve chitinase production by Streptomyces griseorubens C9. This strain was previously isolated and identified from a semi-arid soil of Laghouat region (Algeria). First, syrup of date, colloidal chitin, yeast extract and K₂HPO₄, KH₂PO₄ were proved to have significant effects on chitinase activity using the Plackett–Burman design. Then, an optimal medium was obtained by a Box–Wilson factorial design of response surface methodology in liquid culture. Maximum chitinase production was predicted in medium containing 2% colloidal chitin, 0.47% syrup of date, 0.25 g/l yeast extract and 1.81 g/l K₂HPO₄, KH₂PO₄ using response surface plots of the STATISTICA software v.12.0.     

Aqueous two-phase extraction coupled with ultrafiltration for purification of amyloglucosidase

Aqueous two phase extraction (ATPE) in combination with ultrafiltration was employed for concentration and purification of amyloglucosidase produced by solid state fermentation. After extraction (with water) from dry moldy bran the dilute enzyme extract was concentrated by ATPE in a polyethylene glycol (PEG)/maltodextrin (MDX) system. The enzyme in the top PEG rich phase was then extracted into a Na₂HPO₄ rich bottom phase and further concentrated by ultrafiltration. The partitioning behavior of amyloglucosidase was examined in PEG/MDX, PEG/Na₂SO₄, PEG/Na₂HPO₄, PEG/KH₂PO₄ aqueous two phase systems. Effect of buffering salts such as NaCl, Na₂HPO₄, KH₂PO₄ and Na₂SO₄ on the partitioning behavior of enzyme was studied in PEG/MDX system. Maximum partitioning of amyloglucosidase was seen with KH₂PO₄ (m = 18.1). A two stage ATPE employing PEG/MDX (buffered with KH₂PO₄) and PEG/Na₂HPO₄ systems, followed by ultrafiltration has resulted in an overall recovery of 78.4% with 3.1 fold purification and 9.4 fold concentration of the enzyme.     

Extractable sulphate and organic sulphur in soils and their availability to plants

Ten soils collected from the major arable areas in Britain were used to assess the availability of soil sulphur (S) to spring wheat in a pot experiment. Soils were extracted with various reagents and the extractable inorganic SO₄-S and total soluble S(SO₄-S plus a fraction of organic S) were determined using ion chromatography (IC) or inductively-coupled plasma atomic emission spectrometry (ICP-AES), respectively. Water, 0.016 M KH₂PO₄, 0.01 M CaCl₂ and 0.01 M Ca(H₂PO₄)₂ extracted similar amounts of SO₄-S, as measured by IC, which were consistently smaller than the total extractable S as measured by ICP-AES. The amounts of organic S extracted varied widely between different extractants, with 0.5 M NaHCO₃ (pH 8.5) giving the largest amounts and 0.01 M CaCl₂ the least. Organic S accounted for approximately 30–60% of total S extracted with 0.016 M KH₂PO₄ and the organic C:S ratios in this extract varied typically between 50 and 70. The concentrations of this S fraction decreased in all soils without added S after two months growth of spring wheat, indicating a release of organic S through mineralisation. All methods tested except 0.5 M NaHCO₃-ICP-AES produced satisfactory results in the regression with plant dry matter response and S uptake in the pot experiment. In general, 0.016 M KH₂PO₄ appeared to be the best extractant and this extraction followed by ICP-AES determination was considered to be a good method to standardise on.     

Induction of Growth Increase and Systemic Resistance to Exserohilum turcicum in Maize by Foliar Spray of Phosphates

A single foliar spray of 0.1 M solution of phosphate salts on the upper side of maize (cv. ‘jubilee') leaves 1, 2 and 3 at the 5–6 fully–expanded leaf-stage, 2-4 h before inoculation induced systemic resistance to northern leaf blight caused by Exserohilum turcicum. Nine days after challenge, protection was demonstrated by 91% reduction in the size and 69% in the number of E. turcicum lesions developing on leaves 4, 5, 6 and 7. Appropriate mixing of phosphate solution with KOH revealed that the level of protection was not necessarily dependent on the pH of the solution. The size and number of lesions decreased to 62% and 56%, respectively, 12 days after challenge. There was no damage or chlorotic stipling on the induced leaves (1, 2, and 3) as a result of the phosphate spray. There were no significant differences in the reduction in the number or size of the lesions obtained when the foliar spray was applied 2-4 h or 1, 3, 6, 8, or 10 days before inoculation. One foliar spray ofK₂HPO₄ on leaves 1, 2 and 3 in these intervals before inoculation, remarkably stimulated growth of inoculated plants, which was expressed by several parameters. The possible dual use of phosphate salts as foliar fertilizers and as resistance-inducing agents is discussed     

Studies on isolated cell components: I. Nuclear isolation by differential centrifugation

A method is presented for isolating nuclei of rat and hamster liver in a high state of purity and in a condition optically similar to nuclei within living cells.The isolation procedure consists in the homogenization and differential centrifugation of fresh liver at 0–5 ° in a salt-sucrose solution buffered at pH 7.1. By layering the material to be centrifuged over a relatively large volume of a slightly denser solution the purification can be carried out in 4 or 5 centrifugations. The entire procedure can be completed in about 90 minutes. The yield as determined by measurements of desoxyribonucleic acid is about 5 per cent.The solutions contain KH₂PO₄, K₂HPO₄, NaHCO₃, and sucrose. The sucrose concentration is varied to give density differences required for layering. Salt-sucrose solutions maintain a large proportion of the isolated nuclei in a nongranular condition for 6 hours at 0 °. Pure sucrose is less satisfactory for maintenance.The protein-desoxyribonucleic acid ratio for the isolated nuclei averages 5.1 with a range of 2.7 to 8.9.     

Effect of temperature and pH on absorption of carbon dioxide by a free level of mixed solutions of some buffers

The rate of absorption of carbon dioxide by solutions of NaHCO₃, KH₂PO₄, hydrogencarbonate, phosphate and borate buffers at 20, 30 and 40°C was determined manometrically. The absorption rate increases for all buffers tested with increasing pH. The CO₂ absorption rate by KH₂PO₄ and by the phosphate buffer at low pH is lower than that of water. For other buffers tested it is equal to or higher than that of water, especially at higher temperatures.     

Activation and thermostabilization effects of cyclic 2,3-diphosphoglycerate on enzymes from the hyperthermophilic Methanopyrus kandleri

Enzymes involved in methane formation from carbon dioxide and dihydrogen in Methanopyrus kandleri require high concentrations (> 1 M) of lyotropic salts such as K₂HPO₄/KH₂PO₄ or (NH₄)₂SO₄ for activity and for thermostability. The requirement correlates with high intracellular concentrations of cyclic 2,3-diphosphoglycerate (cDPG; ≈ 1 M) in this hyperthermophilic organism. We report here on the effects of potassium cDPG on the activity and thermostability of the two methanogenic enzymes cyclohydrolase and formyltransferase and show that at cDPG concentrations prevailing in the cells the investigated enzymes are highly active and completely thermostable. At molar concentrations also the potassium salts of phosphate and of 2,3-bisphosphoglycerate, the biosynthetic precursor of cDPG, were found to confer activity and thermostability to the enzymes. Thermodynamic arguments are discussed as to why cDPG, rather than these salts, is present in high concentrations in the cells of Mp. kandleri. Received: 18 June 1998 / Accepted: 24 August 1998     

Accelerated Germination of Maize Seeds Under Chilling Stress by Osmotic Priming and Associated Changes in Embryo Phospholipids

Osmotic priming of maize seeds (Zea mays L. cv. Partap) usingpolyethylene glycol or potassium salts (K₂HPO₄, KH₂PO₄, KNO₃and K₂HPO₄+KNO₃) resulted in accelerated germination at a chillingtemperature (10 °C). The response of seeds primed in solutionsof either 2.5% K₂HPO₄ or 2.5% K₂HPO₄+ KNO₃ was particularlymarked compared with the untreated seeds, and the effect ofpriming was largely retained after seeds had been dried back.All embryo phospholipid fractions and sterols increased duringsalt-priming and the proportion of phospholipid which was diphosphotidylglycerol(DPG) also increased. It is suggested that the marked increasein the DPG content of primed embryos may be due to enhancedinternal organization of their mitochondrial membranes, andthat the benefit of osmotic priming may be at least partly dueto an increased potential for ATP accumulation. Germination, Zea mays L., osmotic priming, phospholipid changes     

Buffering capacity of the chief components of nutritive media for algae

The buffering capacity of solutions of KH₂PO₄ and NaHCO₃ increases with their concentration, the behaviour being describable by mathematical expressions. Solutions of KH₂PO₄ prepared from tap water exhibit a buffering capacity higher by an order of magnitude than those prepared from distilled water. However, there is no difference between the buffering capacities of solutions of NaHCO₃ prepared from tap and distilled water. Urea and NH₄NO₃ have almost no effect on the buffering capacities of sol utions.     

Enhanced curdlan production in <Emphasis Type="Italic">Agrobacterium</Emphasis> sp. ATCC 31749 by addition of low-polyphosphates

A large amount of adenosine triphosphate with high energy phosphate bonds is required for uridine triphosphate regeneration during curdlan biosynthesis by Agrobacterium sp. ATCC 31749. To supply high energy for curdlan synthesis, three low-polyphosphates (Na₄P₂O₇, Na₅P₃O₁₀, and (NaPO₃)₆) with higher energy phosphate bonds were employed to substitute for KH₂PO₄-K₂HPO₄ in fermentation medium. Two genes encoding the polyphosphate metabolizing enzymes, polyphosphate kinase and exopolyphosphatase, were amplified and showed 95% homology to those in Agrobacterium sp. C58 by sequence analysis. The curdlan yields were enhanced by 23 and 134% when phosphate concentrations 0.024 mol/L of Na₅P₃O₁₀ and 0.048 mol/L of (NaPO₃)₆ respectively, were added in the medium. The maximum curdlan yield of 30 ± 1.02 g/L was obtained with the addition of 0.048 mol/L of (NaPO₃)₆ with 5 g/L CaCO₃ in the medium. When CaCO₃ was removed from the culture and the three lowpolyphosphates were added, the pH and biomass yield dropped remarkably and little or no curdlan was produced. The culture containing 0.048 mol/L of (NaPO₃)₆ was mixed with KH₂PO₄-K₂HPO₄ and CaCO₃ in the medium, but showed no effect on curdlan production. However, curdlan yield was improved by 49 ∼ 60% when CaCO₃ was removed from the medium and KH₂PO₄-K₂HPO₄ acted as a buffer. It appears that the positive effect of (NaPO₃)₆ on curdlan production required the buffering capacity of CaCO₃ and the absence of KH₂PO₄-K₂HPO₄ competing as a phosphate supplier.     

Long-term stability of a biofilter treating dimethyl sulphide

 The biofiltration of dimethyl sulphide (Me₂S) and other volatile sulphur compounds results in the accumulation of the metabolite sulphuric acid in the carrier material. Regeneration of an acidified (pH 4.7), Hyphomicrobium-MS3-inoculated compost biofilter degrading Me₂S was not possible by trickling tap water (days 0–28) or a KH₂PO₄/K₂HPO₄ buffer solution (1.26 g PO^3- ₄ l^-1, pH 7) (days 29–47) over the bioreactor at a superficial liquid flow rate of 34 lm^-2 day^-1. Since the protons produced displaced nutrient cations (Na⁺, K⁺, Ca²⁺, Mg²⁺, NH⁺ ₄) from the cation-exchange sites on the compost material, 95% of the SO^2- ₄ was leached as the corresponding sulphate salts and not as sulphuric acid. Concomitantly, the pH of the compost material decreased from 4.7 to 3.9 over the 47 days rinsing period. Moreover, the rinsing procedure resulted in the leaching of essential microbial nutrients from the compost material, such as NH⁺ ₄ (22.3% wash-out over the 47-day rinsing period) and PO^3- ₄ (39.3% washout over the 28-day tap-water rinsing period). However, mixing limestone powder into the Me₂S-degrading compost biofilter was a successful approach to controlling the pH in the optimal range for the inoculum Hyphomicrobium MS3 (pH 6–7). A stoichiometric neutralisation reaction (molar ratio CaCO₃/H₂SO₄=1.1) was observed between the CaCO₃ added and the metabolite of the Me₂S degradation, while high elimination capacities (above 100 g Me₂S m^-3 day^-1) were obtained over a prolonged (more than 100 days) period. Received: 1 December 1995/Received revision: 26 April 1995 Accepted: 29 April 1996     

Synthesis of (R)-2-phenylpropanoic acid from its racemate through an isomerase-involving reaction by Nocardia diaphanozonaria

(R)-2-Phenylpropanoic acid was synthesized from the racemic acid through an isomerization reaction involving resting cells of Nocardia diaphanozonaria JCM3208. The isomerization activity of the cells was enhanced 25-fold by adding 5.5 mM racemic 2-phenylpropanoic acid to the culture medium. When 5 mM racemic 2-phenylpropanoic acid was included in the reaction mixture (4 ml) containing resting cells (100 mg dry cell wt) in 25 mM K₂HPO₄/KH₂PO₄ buffer (pH 7.0) at 30 °C for 8 h, 4.56 mM (R)-2-phenylpropanoic acid (95.8% e.e.) was formed with a 91% molar conversion yield.     

Response-surface methodology for the production and the purification of a new H2O2-tolerant alkaline protease from Bacillus invictae AH1 strain

This work deals with the optimization of the culture conditions of Bacillus invictae AH1 in order to increase the production level of the proteolytic activity. Response-surface methodology (RSM) was applied for the most significant fermentation parameters (concentration of wheat bran and K₂HPO₄/KH₂PO₄) that were earlier identified by Plackett–Burman Design from seven possible factors. A central composite design was used and the quadratic regression model of producing active protease was built. A maximum protease activity was reached and validated experimentally, using a maximum wheat bran concentration (50 g/L) with increased K₂HPO₄/KH₂PO₄ concentration (2.275 g/L). Protease production obtained experimentally coincident with the predicted value and the model was proven to be adequate. Interestingly, the use of RSM increased the protease production by four times (7,000 U/mL) using a low-cost substrate and a culture time of 40 hr, as compared to the standard culture conditions. In the second part of this study, a H₂O₂-tolerant alkaline protease produced from B. invictae AH1 with a molecular mass of about 41 kDa, noted P3, was purified by successive steps of ultrafiltration, gel filtration and ion exchange chromatography. The K _m and V_max values of the purified protease using casein, as substrate, were about 4 mg/mL and 27 μM/min, respectively. The highest enzyme activity was found at pH 9.0 and a temperature of 60°C. In addition, the enzyme showed a quasi-total stability against H₂O₂ (5% for 1 hr) and against most of the tested solid and liquid detergents, suggesting its eventual use in bio-detergent formulations.     

Partitioning of xylanolitic complex from Penicillium janthinellum by an aqueous two-phase system

This work evaluates the influences of five parameters (pH, PEG molecular mass, PEG concentration, concentration of buffer K₂HPO₄–KH₂PO₄ and NaCl concentration) on xylanolitic complex partitioning produced by P. janthinellum in aqueous two-phase systems, using a 2⁵ factorial experimental design. A mathematical model to quantify the influence of these parameters was attained and statistically tested. The optimum point for total protein extraction was obtained under the following conditions: pH 7.0, PEG 10 000, 3.67% PEG, 10% potassium phosphate and 12.4% NaCl. The partition coefficient (K) value experimentally obtained was 5.25 and that predicted by the model was 5.89.     

Sequential liquid-liquid extraction of d-amino acid oxidase from Trigonopsis variabilis

A method for isolation of d-amino acid oxidase (DAAO) from disrupted Trigonopsis variabilis cells has been developed. In an aqueous two-phase system consisting of PEG6000 (220 g l^–1), potassium phosphate (110 g l^–1, K₂HPO₄ + KH₂PO₄ = 10.1:1, mol mol^–1) and dl-methionine (11 g l^–1), the major portion of cellular proteins (87%) was partitioned into the salt phase. By sequential extraction, 48% of DAAO was recovered in PEG phase, giving a yield of 211 U mg protein^–1.