Structural characterization of oligosaccharides and polysaccharides from apple juices produced by enzymatic pomace liquefaction

Eight apple pomace liquefaction juices were produced to characterize soluble cell wall material released by the action of pectolytic and cellulolytic enzyme preparations. Very high colloid values from 9.7 to 19.6 g/L were recovered from the juices by ethanol precipitation. The crude polysaccharides consisted mainly of galacturonic acid (49-64 mol %), arabinose (14-23 mol %), galactose (6-15 mol %), and minor amounts of rhamnose, xylose, and glucose. Separation of the polysaccharides by anion-exchange chromatography yielded one neutral, one slightly acidic, and one acidic polymer accounting for 60% of total colloids. Preparative size exclusion chromatography of the acidic fractions resulted in four polymers of different molecular weights and different sugar compositions. Among them, high molecular weight arabinans and rhamnogalacturonans as well as oligomeric fractions consisting of only galacturonic acid could be found. Linkage studies were performed on neutral fractions from anion-exchange chromatography and size exclusion chromatography. They revealed highly branched arabinans, xyloglucans, and mainly type I arabinogalactans.     

Effect of germination on the carbohydrate composition of the dietary fiber of peas (Pisum sativum L.)

The effect of different conditions of pea germination on dietary fiber (DF) composition was studied. Insoluble dietary fiber (IDF) and soluble dietary fiber (SDF) were subjected to acid hydrolysis, and the resultant neutral sugars, uronic acids, and Klason lignin were quantified. Germinated peas exhibited significantly higher contents of total dietary fiber (TDF) than the raw sample, due to the increases of both DF fractions. Under darkness conditions, germination exhibited the highest contents of IDF and SDF. Decreasing IDF/SDF ratios showed that the carbohydrate changes did not take place to the same extent during germination, the SDF fraction being the most affected. The detailed chemical composition of fiber fractions reveals increases of cellulose in the IDF of germinated samples, whereas SDF exhibits a decrease of pectic polysaccharides and also increases of polysaccharides rich in glucose and mannose. The DF results were corroborated by a comparative examination of the cell wall carbohydrate composition.     

Effect of mash maceration on the polyphenolic content and visual quality attributes of cloudy apple juice

The effects of enzymatic mash treatments on yield, turbidity, color, and polyphenolic content of cloudy apple juice were studied. Using HPLC-ESI-MS, cryptochlorogenic acid was identified in cv. Brettacher cloudy apple juice for the first time. Commercial pectolytic enzyme preparations with different levels of secondary protease activity were tested under both oxidative and nonoxidative conditions. Without the addition of ascorbic acid, oxidation substantially decreased chlorogenic acid, epicatechin, and procyanidin B2 contents due to enzymatic browning. The content of chlorogenic acid as the major polyphenolic compound was also influenced by the composition of pectolytic enzyme preparations because the presence of secondary protease activity resulted in a rise of chlorogenic acid. The latter effect was probably due to the inhibited protein-polyphenol interactions, which prevented binding of polyphenolic compounds to the matrix, thus increasing their antioxidative potential. The results obtained clearly demonstrate the advantage of the nonoxidative mash maceration for the production of cloud-stable apple juice with a high polyphenolic content, particularly in a premature processing campaign.     

Effect of industrial dehydration on the soluble carbohydrates and dietary fiber fractions in legumes

The effects of soaking, cooking, and industrial dehydration treatments on soluble carbohydrates, including raffinose family oligosaccharides (RFOs), and also on total dietary fiber (TDF), insoluble dietary fiber (IDF), and soluble (SDF) dietary fiber fractions were studied in legumes (lentil and chickpea). Ciceritol and stachyose were the main alpha-galactosides for chickpea and lentil, respectively. The processing involved a drastic reduction of soluble carbohydrates of these legumes, 85% in the case of lentil and 57% in the case of chickpea. The processed legume flours presented low residual levels of alpha-galactosides, which are advisable for people with digestive problems. Processing of legumes involved changes in dietary fiber fractions. A general increase of IDF (27-36%) due to the increase of glucose and Klason lignin was observed. However, a different behavior of SDF was exhibited during thermal dehydration, this fraction increasing in the case of chickpea (32%) and decreasing in the case of lentil (27%). This is probably caused by the different structures and compositions of the cell wall networks of the legumes.     

Enzyme-assisted extraction of antioxidative phenols from black currant juice press residues (Ribes nigrum).

Enzymatic release of phenolic compounds from pomace remaining from black currant (Ribes nigrum) juice production was examined. Treatment with each of the commercial pectinolytic enzyme preparations Grindamyl pectinase, Macer8 FJ, Macer8 R, and Pectinex BE, as well as treatment with Novozym 89 protease, significantly increased plant cell wall breakdown of the pomace. Each of the tested enzyme preparations except Grindamyl pectinase also significantly enhanced the amount of phenols extracted from the pomace. Macer8 FJ and Macer8 R decreased the extraction yields of anthocyanins, whereas Pectinex BE and Novozym 89 protease showed no effect. A decrease in pomace particle sizes from 500-1000 microm to <125 microm increased the phenol yields 1.6-5 times. Black currant pomace devoid of seeds gave significantly higher yields of phenols than pomace with seeds and seedless wine pomace. Four selected black currant pomace extracts all exerted a pronounced antioxidant activity against human LDL oxidation in vitro when tested at equimolar phenol concentrations of 7.5-10 microM.     

Soluble and Insoluble Dietary Fiber Content and Composition in Oat

Six oat genotypes were grown in nursery yield trials during 1989-1992 at Lisbon, ND. Groats were analyzed for soluble and insoluble dietary fiber content and composition. Genotype-by-growing year interaction was not significant for soluble or insoluble dietary fiber. Soluble and insoluble dietary fiber differed with genotype (6.0–7.1% and 4.1– 4.9%, respectively) and with growing year (6.0–6.9% and 3.9–5.2%, respectively). The genotype-by-growing year interaction was significant for soluble β-glucan content but not for total neutral sugar or uronic acid content of the soluble dietary fiber. Genotypes did vary in total neutral sugar content but not in uronic acid content. The genotype-by-growing year interaction was not significant for total neutral sugar, β-glucan, uronic acid, or Klason lignin content of insoluble dietary fiber. Genotypes did vary in total neutral sugar, β-glucan, and Klason lignin content but not in uronic acid content of insoluble dietary fiber. The neutral sugar content of soluble dietary fiber was composed of glucose, arabinose, xylose, and galactose. The neutral sugar content of insoluble fiber was composed of glucose, arabinose, and xylose. The content and composition of soluble and insoluble dietary fiber varied with oat genotype. Therefore, oat genotypes could be bred for specific dietary fiber content and composition.     

Impact of Processing on the Noncovalent Interactions between Procyanidin and Apple Cell Wall

Procyanidins can bind cell wall material in raw product, and it could be supposed that the same mechanism of retention of procyanidins by apple cell walls takes place in cooked products. To evaluate the influence of cell wall composition and disassembly during cooking on the cell walls' capacity to interact with procyanidins, four cell wall materials differing in their protein contents and physical characteristics were prepared: cell wall with proteins, cell wall devoid of protein, and two processed cell walls differing by their drying method. Protein contents varied from 23 to 99 mg/g and surface areas from 1.26 to 3.16 m(2)/g. Apple procyanidins with an average polymerization degree of 8.7 were used. The adsorption of apple procyanidins on solid cell wall material was quantified using the Langmuir isotherm formulation. The protein contents in cell wall material had no effect on procyanidin/cell wall interactions, whereas modification of the cell wall material by boiling, which reduces pectin content, and drying decreased the apparent affinity and increased the apparent saturation levels when constants were expressed relative to cell wall weight. However, boiling and drying increased apparent saturation levels and had no effect on apparent affinity when the same data were expressed per surface units. Isothermal titration calorimetry indicated strong affinity (K(a) = 1.4 × 10(4) M(-1)) between pectins solubilized by boiling and procyanidins. This study higllights the impact of highly methylated pectins and drying, that is, composition and structure of cell wall in the cell wall/procyanidin interactions.     

Changes in the cell wall network during the thermal dehydration of alfalfa stems

The effects of heat treatments used to dry alfalfa stems were investigated. Heating at 70 or 100 degrees C caused no major change in the cell wall composition, but xylanase had lower activity on the cell wall of heated material and the amount of xylose released varied with the temperature used. Chemical fractionation of cell wall carbohydrates showed that the main changes occurring during stem dehydration concerned pectic polymers and probably hemicelluloses. There was less material soluble in ammonium oxalate from alfalfa heated at 100 degrees C than from fresh alfalfa. The results suggest that heat processing causes some changes in the cell wall network. Environmental scanning electron microscopy was used to examine fully hydrated tissues at high resolution. There was cell distortion without disruption of cell walls as water was lost.     

Effect of apple cell walls and their extracts on the activity of dietary antioxidants

The effect of dietary fiber in the form of apple cell walls and pectin extracts on natural antioxidants was examined. Cell walls (CW), isolated from apples ( Malus domestica Borkh. cv. "Pacific Rose"), were incubated with ascorbic acid (AA) or quercetin in N-2-hydroxyethylpiperazine- N'-2-ethanesulfonic acid (HEPES) buffer (pH 6.5) at 37 degrees C for 2 h. The resulting supernatants were characterized by a ferric reducing antioxidant power (FRAP) assay and cyclic voltammetry (CV). The experiments were repeated with pectin isolated from the apple cell walls and commercial pectins and showed that polysaccharide preparations stabilized AA effectively but offered little protection against quercetin oxidation. The water-soluble components from cell walls appeared to be responsible for the observed effects of cell-wall polysaccharide preparations on antioxidant activity.     

Chemical composition of natural and polyphenol-free apple pomace and the effect of this dietary ingredient on intestinal fermentation and serum lipid parameters in rats

Unprocessed pomace containing 61% of dietary fiber (DF) and 0.23% of polyphenols (PP) and ethanol- or ethanol/acetone-extracted pomaces containing 66% DF and 0.10% PP and 67% DF and 0.01% PP, respectively, were subjected to a 4 week study in rats. The aim of the study was assessing the advantages of dietary supplementation with the above pomaces. To measure the animal response to dietary treatments, parameters describing cecal fermentation and lipoprotein profile were assessed. The dietary use of 5% unprocessed pomace caused an increase in cecal short-chain fatty acid (SCFA) production and a decrease in blood triacylglycerols, leading to a drop in serum atherogenic index. Ethanol-extracted pomace increased the glycolytic activity of cecal microbiota and decreased cecal branched-chain fatty acid production, whereas acetone extraction led to lower cecal ammonia concentration, decreased colonic pH value, and higher HDL/total cholesterol ratio. The variations in the atherogenic index indicate flavonoids as the key pomace component in relation to blood lipid profile benefits.     

Postharvest storage of white asparagus (Asparagus officinalis l.): changes in dietary fiber (Nonstarch polysaccharides).

Changes occurring in the content and composition of the dietary fiber of white asparagus during storage in different conditions were studied (2 degrees C; 2 degrees C in polyethylene bags with air; 2 degrees C in polyethylene bags with a selected gas mixture). The neutral sugars and uronic acid composition of dietary fiber was determined by gas chromatography and by a spectrophotometric method. The modifications observed in the dietary fiber of the asparagus stored at 2 degrees C were more rapid and pronounced than those in polyethylene bags. The most important changes corresponded to xylose and glucose from insoluble dietary fiber and galactose from soluble dietary fiber. Statistical analysis indicated that the modifications were significantly affected by the type of storage and time.     

Enhancing Water Removal from Whole Stillage by Enzyme Addition During Fermentation

The removal of water from coproducts in the fuel ethanol process requires a significant energy input. In this study, the addition of commercially available cell‐wall‐degrading enzymes was investigated to determine whether or not the enzymes could reduce the amount of water bound within the wet grains. This would have the effect of allowing more water to be removed during centrifugation, reducing the time and energy needed during the drying process. The experiment screened 15 cell‐wall‐degrading enzyme preparations. A significant reduction in water‐binding capacity was found for a number of enzymes tested in the initial screening. The experiment was repeated and two enzymes were identified to have the highest whole stillage dewatering effect, 15 and 14% more water removed for enzyme preparations A and G, respectively. Adding different enzyme preparation amounts to the mash showed varying effects, with the potential to allow for an optimization of enzymes cost and energy savings. In some cases, an enzyme dosage of 0.5 mL worked as well, if not better, than a dosage of 1 mL. These results can translate into improvements in the overall energy efficiency of the process because the wet grains entering the drier would contain less moisture than in the conventional process thus requiring a shorter residence time in the drier.     

Starch and By‐Products from a Laboratory‐Scale Barley Starch Isolation Procedure

Starch was isolated from three different barleys with normal, highamylose, or high‐amylopectin (waxy) starch. The laboratory‐scale starch isolation procedure included crushing of grains, steeping, wet milling, and sequential filtration and washing with water and alkali, respectively. Yield and content of starch, protein, and dietary fiber, including β‐glucan, were analyzed in isolated starch and in the by‐products obtained. Starch yield was 25–34%, and this fraction contained 96% starch, 0.2–0.3% protein, and 0.1% ash. Most of the remaining starch was found in the coarse material removed by filtration after wet milling, especially for the high‐amylose barley, and in the starch tailings. Microscopy studies showed that isolated starch contained mostly A‐granules and the starch tailings contained mostly B‐granules. Protein concentration was highest in the alkali‐soluble fraction (54%), whereas dietary fiber concentration was highest in the material removed by filtration after alkali treatment for the normal and waxy barleys (55%). The β‐glucan content was especially high for the waxy barley in this fraction (26%). The study thus showed that it was possible to enrich chemical constituents in the by‐products but that there were large differences between barleys. This result indicates a need for modifications in the isolation procedures for different barleys to obtain high yields of starch and different by‐products. Valuable by‐products enriched in β‐glucan or protein, for example, may render starch production more profitable.     

Effect of fermentation and autoclaving on dietary fiber fractions and antinutritional factors of beans (Phaseolus vulgaris L.)

The effect of fermentation on antinutritional factors and also on total dietary fiber (TDF), insoluble (IDF) and soluble (SDF) dietary fiber fractions was studied in beans (Phaseolus vulgaris L.). The processes studied were two types of fermentation (lactic acid and natural), and a portion of the obtained flours were processed by autoclaving. The dietary fiber (DF) content and its components were determined using the enzymatic-gravimetric and enzymatic-chemical methods. The TDF content ranged from 24.5% dry matter (DM) in the raw to 25.2% DM in the processed beans. All the processing treatments significantly decreased the SDF content, and irrelevant changes were noticed in the IDF content of processed beans. Cellulose content of all samples was reduced by the processing treatments. Correspondingly, higher amounts of resistant starch was observed in the processed beans, except in the lactic acid fermented ones. However, the levels of pectic polysaccharides and Klason lignin were higher in the samples fermented by Lactobacillus plantarum. The action of microorganisms was determinant for the different degradation of the bean cell wall, disrupting the protein-carbohydrate integration, thus reducing the solubility of DF.     

苹果渣多酚提取工艺的优化

为优化苹果渣中多酚提取工艺,并得到提取工艺和多酚组成之间的关系,利用微波辅助提取法设计了由物料颗粒、液料比、乙醇浓度、微波功率和微波提取时间5个因素构成的多酚提取优化试验流程,构建了涵盖黄酮、原花青素2种典型多酚物质和抗氧化能力的提取工艺评价指标体系。采用证据理论对不同工艺在评价指标下的焦元进行识别,并基于信度函数和似真函数得到了不同提取工艺的效用区间和优化方案。优化结果为：物料颗粒60目,液料比30?mL/g,乙醇体积分数60%,微波功率600?W,提取时间70?s,此条件下苹果渣多酚的提取量为213.83?mg/100g,黄酮提取量为83.21?mg/100g,原花青素提取量为52.79?mg/100g,抗氧化的EC50值为3.71?mg/100mL,验证了采用证据理论进行苹果渣多酚提取工艺优化的有效性。     

Physiological effects of extraction juices from apple, grape, and red beet pomaces in rats

In comparison to classical fruit juice processing, polyphenols and dietary fiber can be extracted from pomace by means of pectinases and cellulases. In the present study, rats were fed with such produced extraction juices from apples, grapes, and red beets as drinking fluids instead of water for 4 weeks to evaluate their physiological effects. In all test groups, the intake of extraction juices was greater as compared to control (water intake), resulting in a higher urine excretion. In the apple and grape group, pH values in feces was lower than control. Administration of extraction juices from apples increased fecal counts of Lactobacillus and Bifidobacterium. More acetate and total short-chain fatty acids appeared in intestinal contents of the apple and red beet group. Furthermore, the intestinal contents of test groups contained higher concentrations of primary bile acids, cholesterol, and cholesterol metabolites but lower concentrations of secondary bile acids. The total amount of steroids excreted by these groups was also greater than control. Quercetin and isorhamnetin appeared in urine of rats fed extraction juices from apples and grapes; in urine of the former group, phloretin was found also. Administration of the extraction juices, enriched in secondary plant metabolites and dietary fiber, resulted in beneficial nutritional effects in rats.     

苹果皮渣固态发酵生产菌体蛋白饲料工艺优化及产物品质分析

为提高苹果皮渣中粗蛋白的含量,以黑曲霉为发酵菌种发酵苹果皮渣,通过单因素试验对影响苹果皮渣固态发酵的参数进行优化,在此基础上进一步采用响应面试验筛选最佳发酵工艺参数,并对最佳工艺条件下的发酵产物品质进行分析。结果表明,黑曲霉发酵苹果皮渣的最佳工艺条件为:黑曲霉接种量10%、发酵温度32℃、水料比3.5、发酵时间6 d。此条件下苹果皮渣经发酵后粗蛋白含量从7.05%提高到33.56%,粗脂肪含量从4.75%提高到5.57%,粗纤维含量从21.80%降低到13.53%,氨基酸总含量从45.10 mg·g~(- 1)提高到126.30 mg·g~(- 1),必需氨基酸含量从16.13 mg·g-1提高到50.40mg·g~(- 1)。综上,黑曲霉发酵可以显著提高苹果皮渣的营养价值,这为苹果皮渣资源化利用、缓解蛋白质供需矛盾提供了有效途径。     

Structural carbohydrate differences and potential source of dietary fiber of onion (Allium cepa L.) tissues.

Onion tissues of three varieties were evaluated for dietary fiber (DF) composition. Insoluble (IDF) and soluble (SDF) dietary fibers were subjected to acid hydrolysis, and the resultant neutral sugars, uronic acids, and Klason lignin were quantified. Brown skin exhibited the highest total dietary fiber (TDF) content (65.8%) on a dry matter basis, followed by top (48.5%) and bottom (38.6%), IDF being the main fraction found. The SDF:IDF ratio decreased from inner to outer tissues. Brown skin and outer leaves byproducts appear to be the most suitable sources of DF that might be used in food product supplementation. The chemical composition reveals that cellulose and pectic polysaccharides were the main components of onion DF in all tissues, although differences between them were noticed. An increase in the uronic acids/neutral sugars ratio from inner to outer tissues was found, suggesting that the galactan side chain shows a DF solubilization role.     

钙处理对葡萄柚果实细胞壁物质代谢及其相关基因表达的影响

【目的】研究采前、 采后钙处理对葡萄柚果实细胞壁组分、 细胞壁降解酶活性变化及其相关基因表达的影响,可为了解钙与果实细胞壁物质代谢之间的关系,揭示钙对果实软化的作用机理,为调控葡萄柚果实膳食纤维含量,提高果实质地品质提供理论依据。【方法】试验于2011年2月至11月在云南省玉溪市葡萄柚果园进行,供试品种为‘里约红’葡萄柚,该品种于2005年嫁接于当地砧木,株行距为3 m×3 m。试验由采前和采后钙处理两部分组成。采前钙处理在幼果初期、 幼果末期、 膨大初期、 膨大末期、 转色期,叶面喷施2% CaCl2; 采后钙处理在果实成熟采后浸于2% CaCl2溶液5 min, 室温贮藏。之后每15天取样一次,每次取10个果实,测定葡萄柚果肉细胞壁组分、 细胞壁降解酶活性及其基因表达量。【结果】随葡萄柚果实后熟软化,紧密结合型果胶(共价结合型果胶)解聚为松散结合型果胶(水溶性果胶、 离子结合型果胶),紧密结合型半纤维素(24% KOH可溶性半纤维素)解聚使其含量下降,而松散结合型半纤维素含量增加(4%KOH可溶性半纤维素)。果实PG、 PME、 Cx、 α-L-Af和β-Gal酶活性及其基因表达量均随果实软化呈不同程度增加。PME活性在果实采收后表现出较高含量,而PG活性在果实贮藏前期急剧增加,其酶基因的表达量与酶活性变化趋势基本一致。Cx、 α-L-Af和β-Gal活性在贮藏中、 后期上升较快,相关酶基因的表达量亦明显增加。钙处理显著地降低果实细胞壁降解酶活性和基因表达水平,其中采后钙处理对α-L-Af和β-Gal活性和基因表达在贮藏中、 后期的调控作用较显著,酶活性和基因表达均维持在较低水平。【结论】外源钙处理降低细胞壁降解酶活性及其基因表达,抑制了细胞壁物质的解聚,采后钙处理对细胞壁物质代谢的调控效果优于采前钙处理。外源钙处理抑制了细胞壁降解酶基因表达水平,降低了细胞壁降解酶活性,减缓了果胶、 半纤维素的解聚,从而达到调控果实膳食纤维含量、 维持果实质地品质、 延长果实货架期寿命的目的。     

混施微生物菌剂和有机肥对‘新红星’苹果解袋后果实品质的影响

以5年生‘新红星’苹果果树为试材,探究不同施肥处理(T1,有机肥;T2,微生物菌剂+有机肥;T3,微生物菌剂;CK,对照)对‘新红星’苹果解袋后果实内在品质、呼吸速率、乙烯释放率、果实硬脆性及相关酶和基因表达的影响。结果表明,与传统单一施肥相比,施加含微生物菌剂的有机肥显著提高了果实可溶性固形物含量、可溶性糖含量及糖酸比。解袋后0~12 d果实呼吸速率及乙烯释放速率显著上升,12~15 d趋于平稳。果实解袋后第9、12、15 d,T2组果实可溶性固形物含量相对于CK组高出2.63%、5.89%、8.78%;可溶性糖高出6.89%、6.71%、12.86%;糖酸比高出15.85%、19.25%、17.08%,且差异显著。施加含微生物菌剂的有机肥处理(T2)显著提高了果实的总香气含量,其含量相对于CK、T1、T3组分别高出16.69%、9.06%、6.25%。混施微生物菌剂和有机肥有利于解袋后苹果果实着色,使果皮细胞排列紧密整齐,对提升果实脆度,减缓果实硬度下降具有重要作用。细胞壁关键酶果胶甲酯酶(PME)、多聚半乳糖醛酸酶(PG)活性在解袋后一直处于上升状态,其中T2组PME、PG活性及MdPME、MdPG表达量均低于CK组,因此果实在解袋后保持较高的硬脆度。综上所述,混施微生物菌剂和有机肥(T2)对提高‘新红星’苹果果实品质及延长货架期具有重要作用。