Effects of Particle Size and Starch Damage of Flour and Alkaline Reagent on Yellow Alkaline Noodle Characteristics

A hard white spring wheat was milled to yield three patent flours with different starch damage levels by manipulating reduction grinding conditions, and each flour was sieved to give three different particle sizes (85–110, 110–132, 132–183 μm). Raw alkaline noodles were prepared using either 1% w/w kansui (sodium and potassium carbonates in 9:1 ratio) or 1% w/w sodium hydroxide. Noodles prepared with sodium hydroxide were significantly brighter, less red, and more yellow than those made with kansui. Differences in noodle color among flour treatments were evident but were attributable to differences in flour refinement rather to than particle size or starch damage. Noodles were rested for 1 hr after processing before cooking. Alkaline reagent was the main factor associated with cooking loss, being ≈50% greater for sodium hydroxide noodles because of higher pH compared with kansui noodles. Cooked sodium hydroxide noodles were thicker than kansui noodles, and cooked strands for both noodle types became thicker as starch damage increased and as particle size became coarser. Instrumental assessment of cooked noodle texture showed that maximum cutting stress (MCS), resistance to compression (RTC), recovery (REC), stress relaxation time (SRT), chewiness (CHE), and springiness (SPR) were influenced by the type of alkaline reagent. Flour particle size and starch damage also influenced noodle texture but the magnitude of the effects and the trends were dependent on alkaline reagent. MCS of kansui noodles was much greater than for sodium hydroxide noodles. MCS of kansui noodles increased as starch damage increased but, in contrast, MCS of sodium hydroxide noodles decreased with increasing starch damage. REC of kansui noodles increased with increasing starch damage and decreased with larger particle size, whereas for sodium hydroxide noodles REC decreased with increasing starch damage and declined dramatically with larger particle size. Kansui noodles exhibited significantly shorter SRT than sodium hydroxide noodles. SRT of kansui noodles was only moderately affected by starch damage and particle size, whereas for sodium hydroxide noodles, SRT became much shorter as flour became coarser and starch damage became higher. CHE of kansui noodles was greater than for sodium hydroxide noodles. CHE of kansui noodles increased as starch damage increased. In contrast, CHE of sodium hydroxide noodles decreased as starch damage increased and also decreased as flour became coarser. SPR of both noodle types decreased as flour became coarser and starch damage became greater. On the basis of these experiments, flour of smaller particle size is an asset to the cooking quality of sodium hydroxide noodles, but high starch damage is to be avoided. For kansui noodles, the impact of flour particle size on cooked noodle texture was less evident and low starch damage, rather than high starch damage, was an asset.     

Influence of pH, benzoic acid, glutathione, EDTA, 4-hexylresorcinol, and sodium chloride on the pressure inactivation kinetics of mushroom polyphenol oxidase.

Pressure inactivation of mushroom PPO was studied for pH values ranging from 4 to 8, and the effect of some antibrowning agents on the pressure stability of mushroom PPO at pH 6.5 was evaluated. pH reduction below 6.5 resulted in a lowered inactivation threshold pressure and an increase of the absolute value of the activation volume (or a decrease of the z(p) value), the latter two parameters reflecting the pressure dependency of the inactivation rate constant. An increase in pH from 6.5 to 8, on the other hand, did only marginally affect the pressure stability of the enzyme. Mushroom PPO at pH 6.5 was markedly sensitized toward pressure by the presence of 2.5 mM 4-hexylresorcinol and slightly stabilized by the presence of 5 mM EDTA. The presence of 5 mM glutathione, sodium chloride, or benzoic acid caused no significant alteration of the enzyme pressure stability. Only in the presence of 4-hexylresorcinol, significant changes of the activation volume and z(p) value were noticed.     

Effect of ph on amount of phosphorus extracted by 10 mm calcium chloride from three Rothamsted soils

Abstract

Three silty clay loams from the classical field experiments at Rothamsted Experimental Station (UK) with low phosphorus (P) status were treated with phosphate fertilizer and incubated for 15 days at field capacity with added acid [hydrochloric acid (HCl)] or base [sodium hydroxide (NaOH)] to give pH ranges measured in 1:5 suspensions of soil in 10 mM calcium chloride (CaCl₂) of 6.3–8.7 (Hoosfield A, pH 8.2), 3.8–8.2 (Hoosfield B, pH 6.3), and 2.8–7.1 (Geescroft, pH 5.3). Extractable ? was measured by the 10 mM CaCl₂ extraction procedure. For the Hoosfield ? and Geescroft soils without added phosphate fertilizer, extractable ? was decreased at both ‘low’ and ‘high’ pH values, the maximum being at about 5.4 in both soils. In the calcareous Hoosfield soil, extractable ? decreased with increasing pH over the range studied. These changes in extractable ? were magnified in soils treated with phosphate fertilizer but the maxima and trends were unaltered. The results indicate that native soil ? appears to be changed by pH in the same way as added ? to the soil. In the calcareous Hoosfield A soil, added acid did not reduce soil pH to less than 6.4 (because of its high buffer capacity) and so the pH level for maximum ? solubility was not found.     

Hydrolytic products and kinetics of triazophos in buffered and alkaline solutions with different values of pH

The hydrolysis of triazophos was studied in buffered solutions in the range of pH 4-10 and in sodium hydroxide solutions with pH values up to 12. The results showed that the degradation of triazophos in the above solutions followed simple pseudo-first-order kinetics. At 35 degrees C, the rate constants in buffered solutions ranged from 0.0222 d(-1) at pH 4 to 0.5357 d(-1) at pH 10, and increased to 0.6251 h(-1) in 0.01 mol/L sodium hydroxide solution. The results also indicated that the base-catalysis was more important than acid-catalysis in the hydrolysis of triazophos. On the basis of the Arrhenius plot, the calculated activation energy (E(a)) and the frequency factor (A) for the hydrolysis of triazophos in buffered solution of pH 10 were 78.6 kJ/mol and 1.13 x 10(13) d(-1), respectively. Hydrolytic products of triazophos in buffered solutions of pH 4 and 10, as well as in sodium hydroxide solution of pH 11, were identified as their corresponding trimethylsilyl derivatives with a gas chromatography-mass spectrometer (GC-MS). The possible hydrolytic pathways of triazophos were also proposed.     

Comparison of Prewashing Procedures for the Assessment of Phosphate Rock Dissolution in Soils

When evaluating phosphate rock (PR) dissolution, previous to the extraction with sodium hydroxide (NaOH), dry soil samples with PR were extracted with three solutions to remove exchangeable and solution calcium (Ca) [sodium chloride (NaCl) 1 M, buffered NaCl with ethylenediaminetetraacetic acid (EDTA) (NaCl–EDTA), and NaCl buffered at pH 7 with triethanolamine (TEA) (NaCl–TEA)] for comparison with the extraction of soil samples without any prewash. In acidic soils, up to 51% of applied P was recovered during the NaCl extraction because of the high exchangeable acidity released during the extraction. In soils with exchangeable Ca>2 cmol₍₊₎kg^?1, high EDTA quantities also promoted PR dissolution. The NaCl–TEA solution efficiently removed Ca, avoiding PR dissolution and P retention by calcium hydroxide [Ca(OH)₂] during the NaOH extraction. Thus, when evaluating PR dissolution we recommend the use of NaCl–TEA to remove Ca. We also recommend the same procedure when applying the Chang and Jackson fractionation to calcareous soils and soils submitted to PR application.     

Effect of bruising on respiration, superficial color, and phenolic changes in fresh Manzanilla olives (Olea europaea pomiformis): development of treatments to mitigate browning

The aim of the work was to study the postharvest changes in Manzanilla olives and to find treatments to mitigate damages because of bruises. The phenolic content in bruised and unbruised fruits exposed to air always decreased, but the loss in phenols and the respiratory activity were greater in bruised olives; these changes were related to the appearance of brown spots. Immersion of the picked fruits in a cold (8 °C) acidic solution (pH 3), ascorbic acid solution (100 mM), or sodium metabisulfite solution (100 mM) significantly reduced the loss in phenols in olives and led to lighter brown bruised areas. This immersion did not affect the behavior of the fruits during the lye treatment and the subsequent fermentation. In the final product, no influence on the surface color of unbruised olives was observed and there was a significant color improvement in the bruised areas of damaged olives.     

Preventing lipid oxidation during recovery of functional proteins from herring (Clupea harengus) fillets by an acid solubilization process

It has previously been found that a process based on solubilization at pH 2.7 gives high yields of herring muscle proteins with good functionality. In this study, the development of lipid oxidation during acid processing of herring mince was studied. It was tested how modifications of the process conditions and/or additions of antioxidants could prevent lipid oxidation during the actual process and then during ice storage of the protein isolates. Processing parameters evaluated were prewash of the mince, exposure time to pH 2.7, inclusion or exclusion of a high-speed centrifugation, and addition of antioxidants. Antioxidants tested were erythorbate (0.2%, 9.3 mM), sodium tripolyphosphate (STPP; 0.2%, 5.4 mM), ethylenediaminetetraacetic acid (EDTA; 0.044%, 1.5 mM), and milk proteins (4%). The first three antioxidants were added in the prewash or during the homogenization step, whereas milk proteins were added to the final precipitate. At time 0, all isolates were analyzed for pH, moisture content, and thiobarbituric reactive substances (TBARS). Selected isolates were also analyzed for lipid and protein content. Stability during ice storage was followed in terms of odor, TBARS, and color (a/b values). Extensive lipid oxidation took place using the "control" process without high-speed centrifugation. This was not significantly (p < or = 0.05) affected by a prewash or varied exposure time to pH 2.7. Including high-speed centrifugation (20 min, 10,000g) significantly (p < or = 0.05) reduced TBARS values, total lipids, a values and b values. Erythorbate alone, or in combination with STPP/EDTA, significantly (p < or = 0.05) reduced lipid oxidation during processing if added in the prewash or homogenization step. During ice storage, better stability was gained when antioxidants were added in both of these steps and when EDTA was used instead of STPP.     

Die Veränderung von Huminsäuren in alkalischer Lösung

The change of humic acids in alkaline solution Five natural humic acids were fragmented under the conditions of the conventional method of extraction of humic substances with sodium hydroxide. Fulvic acid, hymatomelanic acid and a water soluble fraction (at pH 2) could be isolated as fragmentation products. The three fractions were formed directly after the treatment with sodium hydroxide, their quantities depend on the concentration and time of treatment with sodium hydroxide and from the function of the system. The deviating, differentiating and reproducing formation of fragments is explained by partial reversible reactions. Therefore fulvic acid and hymatomelanic acid must be regarded as artefacts. existing during the procedure of isolation of humic substances at high pH-values. Therefore the conventional isolation of humic substances from soils should always be accompanied by experiments, which inform about the arteficial production of ‘fulvic acids’ and ‘hymatomelanic acids’ during the procedure of isolation.     

高静压加工对黄桃罐头品质的影响（英）

为拓展非热加工技术在水果罐头加工中应用,以黄桃罐头为试材,研究了高静压加工对黄桃罐头品质的影响。分析了黄桃罐头果肉或汤汁的质地、显微结构、色泽、pH值、可滴定酸和可溶性固形物在加工前后变化,并与传统热加工产品进行比较。结果表明：高静压加工（600 MPa, >5 min）能有效地保持产品质地、显微结构、色泽、pH值、可滴定酸和可溶性固形物,而热加工（90±2°C, 20 min）导致果肉质地软化、显微结构破坏及可溶性固形物增加,严重影响产品品质。同时感官分析表明,与对照相比,高静压加工黄桃罐头除新鲜度及滋味稍差外,其他方面均无明显差别,而热处理黄桃罐头除保持较好色泽与香气外,其他方面均产生劣质的影响。所得研究结果将为高静压技术在水果罐头中工业化应用提供理论依据。     

Extraction of Wheat Starch with Aqueous Sodium Hydroxide

Wheat starch was extracted with aqueous sodium hydroxide at 30–38% starch solids, pH 11.5–12.3, and 25–42°C for 0.17–24 hr. Stirring wheat starch at pH 12.3 and 25°C for 3 and 24 hr, then washing with water, neutralizing, and washing again, removed 70 and 90% phosphorus (P), respectively. Adding 16% sodium sulfate (dry starch basis) into the alkaline medium removed ≈80% of P at pH 12.0 and 25°C in 3 hr and >95% of P at pH 11.7 and 42°C in 3 hr. Sulfate ion was absorbed strongly by wheat starch in aqueous sodium hydroxide at pH 12.0, and sodium sulfate also increased the starch's uptake of hydroxide ion. Low-P wheat starch (>90% of P removed) retained the fatty acids in the untreated starch, but a fatty acid-amylose complex was not detectable by differential scanning colorimetry. The enthalpy of gelatinization of the low-P wheat starch almost matched that of prime starch, as did its X-ray diffraction pattern. Those data are consistent with saponification of the lysophospholipid in the amorphous phase of the starch to form fatty acid salts and glycerol-choline or glycerol-ethanolamine phosphodiesters that slowly diffused out of the granules. The low-P wheat starch was judged to have less “cereal” odor than the prime starch, and its pasting temperature at 9.3% starch solids was lowered by ≈10°C.     

Separation of food grade antioxidants (synthetic and natural) using mixed micellar electrokinetic capillary chromatography.

A capillary electrophoretic method, for the determination of antioxidants present in food, has been developed using mixed micellar electrokinetic capillary chromatography. The buffer consists of sodium cholate (40 mM), sodium dodecyl sulfate (15 mM), 10% methanol, and 10 mM borate at pH 9.3. A separation was obtained for nine antioxidants (synthetic and natural) commonly found in food. High-performance liquid chromatography and capillary electrophoresis were applied to the analysis of sesame oil and wine. Ascorbic acid was identified in wine.     

Anthocyanins, flavonols, and free radical scavenging activity of Chinese bayberry (Myrica rubra) extracts and their color properties and stability

Characterization of anthocyanins and flavonols and radical scavenging activity assays of extracts from four Chinese bayberry (Myrica rubra) varieties with different fruit colors were carried out. One dominant anthocyanin and three major flavonols were isolated by HPLC, and cyanidin-3-O-glucoside and two of three flavonols, myricetin and quercetin-3-O-rutinoside, were identified by cochromatography with authentic standards. Both DPPH* and ABTS*(+) cation assays indicated that the black varieties (Biji and Hunan) demonstrated much higher radical scavenging activities than the pink (Fenhong) and yellow (Shuijing) varieties, which may be attributed to much higher levels of anthocyanins, flavonoids, and total phenolics in the black varieties. Biji and Hunan had 6.49 and 6.52 mM Trolox equivalent antioxidant capacity (TEAC) per 100 g of fresh weight, whereas the pink (Fenhong) and yellow (Shuijing) bayberries had 1.32 and 1.31 mM TEAC/100 g. Different fruit color was reflected by the surface color and pigment extract color. Color stability of the pigment was dependent on pH, and the pigment was more stable at low pH (pH approximately 1.5). The lightness (L) increased while the chroma (C value) decreased with increase of pH until pH 5, but higher pH caused a small decrease for L and an increase for C.     

Determination of gibberellic acid in fermentation broth and commercial products by micellar electrokinetic chromatography

Micellar electrokinetic chromatography (MEKC) was developed as a method for quantitative determination of gibberellic acid (GA3) in fermentation broth and commercial products, using 25 mM disodium tetraborate as a buffer at pH 9.2 and 100 mM sodium dodecyl sulfate as a micellar phase. The baseline resolution (Rs of GA3 from other compounds in fermentation broth was achieved with Rs > 2.5. The addition of methanol or acetonitrile in the MEKC buffer did not give a better resolution. Advantages of this MEKC method include high accuracy and precision and no sample preparation except for dilution and filtration.     

Isolation of Hemicellulose from Corn Fiber by Alkaline Hydrogen Peroxide Extraction

For the first time, alkaline hydrogen peroxide (AHP) extraction conditions were used to isolate hemicellulose (arabinoxylan) from destarched corn fiber. Yields of the water-soluble hemicellulose B ranged from 35% (24 hr extraction at 25°C) to 42% (2 hr extraction at 60°C). The hemicellulose B resulting from the 2 hr extraction (pH 11.5) was off-white in color, and a very low proportion (1.7%) of water-insoluble hemicellulose A was extracted. AHP treatment caused delignification and facilitated the alkaline extraction of hemicellulose from the lignocellulosic fiber matrix. In the absence of H₂O₂, yields were reduced by more than one-third when using otherwise identical extraction conditions of time, temperature and pH. In the standard protocol, corn fiber, NaOH solution, and H₂O₂ were mixed in a 1:25:0.25 (w/v/w) ratio. Extractions were conducted at pH 11.5 at 25°C or 60°C. The pH was adjusted to 11.5 by addition of NaOH at ambient and elevated temperatures. The optimum hemicellulose yield (51.3%; dry, starch-free basis) was obtained when the pH was increased to 12.5 for the final one-half of the extraction period. Products obtained after extraction at pH values greater than 11.5 were tan in color, however, and the goal of the research has been to isolate white hemicellulose B and then evaluate its properties. Under most conditions, the yields ofhemicellulose B, potentially the most useful form for food and industrial applications, exceeded those of hemicellulose A by more than 10-fold. The hemicellulose B products were lighter in color than those obtained using traditional alkaline extraction conditions of refluxing with calcium or sodium hydroxide. Steps prior to extractions with alkaline H₂O₂, such as grinding to 20 mesh and extracting with azeotropic toluene-ethanol, were found to be unnecessary.     

Effects of silicon on the germination,growth and physiology activity of Zea mays L. seedlings under PH stress

Silicon(Si) has a significant function in reducing abiotic stresses on plants. pH stress is one of abiotic stresses. We investigated the effects of silicon on maize seedlings under pH stress. The results showed that incorporation of Si (2.0?mM (mmol)) into pH 3.0 increased the growth, chlorophyll and carotenoid contents, decreased catalase, peroxidase and ascorbate peroxidase enzyme activity and malondialdehyde content. The combined treatments with Si (8.0?mM) and pH 3.0 decreased the maize growth compare with the single pH (3.0). Incorporation of Si (2.0 or 8.0?mM) into pH 8.0 were obviously unchanged compare with the single pH (8.0). The combined or single effects of Si (2.0 or 8.0?mM) and pH (3.0 or 8.0) on germination percentage were negligible. The application of Si (2.0?mM) could be a better strategy for improving the plant growth and alleviating low pH stress in soil.     

Effect of different forms of alkali treatment on specific fermentation inhibitors and on the fermentability of lignocellulose hydrolysates for production of fuel ethanol

Treatment with alkali, particularly overliming, has been widely used as a method for the detoxification of lignocellulose hydrolysates prior to ethanolic fermentation. However, the mechanisms behind the detoxification effect and the influence of the choice of cation have not been well understood. In this study, a dilute acid hydrolysate of spruce and an inhibitor cocktail consisting of six known inhibitors were used to investigate different alkali detoxification methods. The various treatments included the addition of calcium hydroxide, sodium hydroxide, potassium hydroxide, and ammonia to pH 10.0 and subsequent adjustment of the pH to 5.5 with either sulfuric or hydrochloric acid as well as treatment with the corresponding amounts of calcium, sodium, and potassium as sulfate or chloride salts at pH 5.5. An RP-HPLC method was developed for the separation of 18 different inhibitors in the hydrolysate, including furaldehydes and phenolics. Detection and quantification were carried out by means of UV, DAD, and ESI-MS in negative mode. Treatment of the spruce hydrolysate with alkali resulted in up to approximately 40% decrease in the concentration of furaldehydes. The effects on the aromatic compounds were complex. Furthermore, SFE was performed on the precipitate formed during alkali treatment to evaluate the inhibitor content of the precipitate, and the following RP-HPLC analysis implied that potential inhibitors were removed mainly through conversion rather than through filtration of precipitate. Parallel experiments in which sulfuric acid or hydrochloric acid was used for acidification to pH 5.5 after alkali treatment indicated that the choice of anion did not affect the removal of inhibitors. Detoxification with calcium hydroxide and ammonia resulted in better fermentability using Saccharomyces cerevisiae than detoxification with sodium hydroxide. The results from the experiments with the inhibitor cocktail indicated that the positive effects of alkali treatment are difficult to explain by removal of the inhibitors only and that possible stimulatory effects on the fermenting organism warrant further attention.     

不同预处理方式对柳枝稷厌氧发酵性能的影响

以柳枝稷为原料,研究微波,蒸汽加热和NaOH预处理方法对柳枝稷的结晶度和纤维结构的影响,同时考察了预处理后的柳枝稷在中温时的厌氧发酵性能.结果显示:3种处理都可以降低原料的结晶度;微波和NaOH处理可以显著降低柳枝稷的中性洗涤纤维、酸性洗涤纤维、木质素等含量;NaOH处理会降低粗脂肪的含量;蒸汽加热处理和原料的累积产气量(28 486和28 686 mL)及产气率(453.60和456.79mL/g)接近,而NaOH预处理由于C/N较高、阳离子毒害作用和抑制物的作用使得厌氧发酵性能降低.可见预处理可以降低柳枝稷纤维含量,但是对厌氧发酵性能并无明显改善作用.     

Determination of phenol in honey by liquid chromatography with amperometric detection

A sensitive, selective analytical method has been developed for determination of phenol in honey by liquid chromotography (LC) with amperometric detection (AMD). Phenol is extracted with benzene from the distillate of honey. The benzene extract is washed with 1% sodium bicarbonate solution and then reextracted with 0.1N sodium hydroxide followed by cleanup on a C18 cartridge. Phenol is determined by reverse-phase LC with amperometric detection. An Inertsil ODS column (150 X 4.6 mm, 5 microns) is used in the determination. The mobile phase is a mixture (20 + 80 v/v) of acetonitrile and 0.01M sodium dihydrogen phosphate containing 2mM ethylenediaminetetraacetic acid, disodium salt (EDTA) with the pH adjusted to 5.0. The flow rate is 1 mL/min under ambient conditions. The applied potential of the AMD using a glassy carbon electrode is 0.7 V vs an Ag/AgCl reference electrode. Average recoveries of phenol added to honey were 79.8% at 0.01 ppm spiking level, 90.4% at 0.1 ppm, and 91.0% at 1.0 ppm. Repeatabilities were 3.4, 1.3, and 1.8%, respectively. The detection limit of phenol in honey was 0.002 ppm. For analysis of 112 commercial honey samples, the range and average values of 32 detected samples were 0.05-5.88 ppm and 0.71 ppm, respectively.     

Purification and characterization of polyphenol oxidase from cauliflower (Brassica oleracea L.)

Polyphenol oxidase (PPO) of cauliflower was purified to 282-fold with a recovery rate of 8.1%, using phloroglucinol as a substrate. The enzyme appeared as a single band on sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE). The estimated molecular weight of the enzyme was 60 and 54 kDa by SDS-PAGE and gel filtration, respectively. The purified enzyme, called phloroglucinol oxidase (PhO), oxidized phloroglucinol (K(m) = 3.3 mM) and phloroglucinolcarboxylic acid. The enzyme also had peroxidase (POD) activity. At the final step, the activity of purified cauliflower POD was 110-fold with a recovery rate of 3.2%. The PhO and POD showed the highest activity at pH 8.0 and 4.0 and were stable in the pH range of 3.0-11.0 and 5.0-8.0 at 5 °C for 20 h, respectively. The optimum temperature was 55 °C for PhO and 20 °C for POD. The most effective inhibitor for PhO was sodium diethyldithiocarbamate at 10 mM (IC(50) = 0.64 and K(i) = 0.15 mM), and the most effective inhibitor for POD was potassium cyanide at 1.0 mM (IC(50) = 0.03 and K(i) = 29 μM).     

Effect of storage process on the sugars, polyphenols, color and microbiological changes in cracked Manzanilla-Aloreña table olives

The green cracked "seasoned" Manzanilla-Alore?a table olive is a specialty with a high demand when prepared from fresh fruits; however, when stored fruits are used, the product loses its green color, presents a brownish tone, and loses demand. Different alternative storage systems for preventing such changes and preserving the freshness of the fruits were studied, and their effects on sugar, polyphenol, color, and microbiological changes were analyzed. The application of two washing waters in the presence of different compounds before brining markedly decreased the sugar and polyphenol contents in the flesh, without negatively influencing the color; it also caused the inhibition of yeasts and lactic acid bacteria (except in treatments using sodium metabisulfite and saturated carbon dioxide (CO(2)) in the storage olive brines. Salicylic acid inhibited microbial growth during washings and storage. The best long-term color was achieved in the presence of sodium metabisulfite. A combination of two washing waters (containing 5% sodium chloride (NaCl) and 0.1% sodium metabisulfite or saturated CO(2)), followed by immersion of the fruits in 15% NaCl brine with 0.1% sodium metabisulfite or brine under saturated CO(2) added, led to the best storage conditions.