Glycoside Hydrolase Family 51 α‐l‐Arabinofuranosidases from Clostridium thermocellum and Cellvibrio japonicus Release O–5‐Feruloylated Arabinose

Arabinofuranosidases act synergistically with other enzymes to depolymerize arabinoxylans by cleaving arabinofuranose substituents from the β‐(1→4)‐linked d ‐xylopyranose backbone. Because arabinose feruloylation is a barrier to some, but not all, arabinofuranosidases, we investigated the actions of three α‐l ‐arabinofuranosidases from the glycoside hydrolase (GH) family 51 on feruloylated arabinoxylan‐oligosaccharide standard compounds with and without feruloyl esterase. GH51 α‐l ‐arabinofuranosidases from Clostridium thermocellum and Cellvibrio japonicus both partially released feruloylated arabinose (up to 59% for C. thermocellum). Simultaneous incubation with arabinofuranosidases and feruloyl esterase quantitatively released arabinose from feruloylated standard compounds. Therefore, although feruloylation does not completely obstruct GH51 arabinofuranosidases, synergistic approaches utilizing multiple enzymes remain the most effective tactic for enzymatic breakdown of feruloylated compounds.     

Structural Characteristics of Water‐Extractable Nonstarch Polysaccharides from Barley Malt

Water‐extractable (WE) material was isolated from a Canadian barley malt (cv. Harrington). The purified WE material contained mainly arabinoxylans, β‐glucans, proteins, and small amounts of arabinogalactans and mannose‐containing polymers. WE material was treated with specific enzymes to obtain two fractions: one enriched in arabinoxylan (AX) and another enriched in β‐glucan (BG). The AX fraction was further fractionated by stepwise precipitation in (NH₄)₂SO₄ into five arabinoxylan subfractions. ¹H‐NMR spectroscopy and sugar analyses revealed a relatively high content of unsubstituted xylose residues (48–58%) as well as a relatively high content of doubly substituted xylose residues (28–33%) in the structure of the arabinoxylans. β‐Glucans constituted a minor portion of water‐extractable malt polysaccharides and were characterized by high levels of tri‐ and tetrasaccharide residues (93.4%) with a molar ratio of 2.19 for cellotriosyl to cellotetraosyl units. Size‐exclusion chromatography revealed that the WE material contained several polymer populations. One population had a very high molecular weight that appeared to be the result of aggregation. The AX fraction contained higher molecular weight polymers than the BG fraction.     

Isolation and Characterization of Water‐Extractable Arabinoxylan from Hull‐less Barley Flours

A new procedure was developed for the isolation of highly purified water‐extractable arabinoxylan (WE‐AX) from hull‐less barley flour. It included inactivation of endogenous enzymes, removal of proteins with silica gel, and removing β‐glucans, arabinogalactan‐peptides, and starch fragments by enzyme or solvent precipitation steps. WE‐AX recovered by this isolation procedure represented, on average, 47% of all WE‐AX present in hull‐less barley flour. Purified WE‐AX from flour of different hull‐less European barley cultivars contained 84.9–91.8% AX and showed small structural differences. The apparent peak molecular weight of the purified WE‐AX was 730,000–250,000, and the arabinose‐to‐xylose ratio was 0.55–0.63. Proton nuclear magnetic resonance spectroscopy showed that the levels of un‐, O‐2 mono‐, O‐3 mono‐, and O‐2,O‐3 disubstituted xylose residues were 59.1–64.7%, 8.2–10.0%, 5.7–10.6%, and 17.6– 23.1%, respectively, and the ratio of di‐ to monosubstituted xylose was 0.90–1.54. Both O‐3 mono‐ and disubstituted xylose residues occurred isolated or next to disubstituted xylose residues in the WE‐AX chain.     

Antioxidant Capacity of Water‐Extractable Arabinoxylan from Commercial Barley,Wheat, and Wheat Fractions

The objective of this research was to analyze the antioxidant capacity directly of water‐extractable nonstarch polysaccharides (NSP) and feruloylated arabinoxylans (WEAX) following their characterization. NSP were isolated from barley, wheat, and wheat fractions (germ, bran, and aleurone). WEAX were extracted only from wheat fractions. Antioxidant capacity of NSP measured with the 2,2‐diphenyl‐1‐picrylhydrazyl (DPPH), 2,2′‐azino‐bis(3‐ethylbenzothiazoline‐6‐sulfonic acid (ABTS), and oxygen radical absorbance capacity (ORAC) assays was 24.0–99.0, 40.0–122.0, and 140.0–286.0μM Trolox equivalents (TE)/g, respectively. The antioxidant capacity of WEAX was 75.7–84.0, 58.0–105.0, and 110.0–235.0μM TE/g for those three assays. DPPH and ABTS were highly correlated to xylose content (R² = 0.85), degree of substitution (R² = −0.99), total phenolic acids (R² = >0.73), total phenolic content (TPC) (R² = >0.78), and ferulic acid content (R² = >0.86). ORAC was only influenced by TPC (R² = 0.63). By taking yield and antioxidant capacity into account, NSP would provide about 0.4–4.2, 0.6–5.1, and 2.8–12.0μM TE/g of flour of radical scavenging activity as measured by DPPH, ABTS, and ORAC, respectively, compared with WEAX (0.4–1.0, 0.3–1.3, and 0.6–2.8μM TE/g). Our results suggest that NSP or WEAX may play a role in protection against free radicals in a food matrix and likely in the gastrointestinal tract.     

Pectic Arabinans in Quinoa Seeds (Chenopodium quinoa Willd.) Are Acylated with p‐Coumaric Acid

A modified digestion method was used to hydrolyze large amounts of quinoa meal to study polysaccharide‐bound phenolic acids. Besides the well‐characterized oligosaccharide O‐(2‐O‐trans‐feruloyl‐α‐l ‐arabinofuranosyl)‐(1→5)‐l ‐arabinofuranose, O‐(2‐O‐trans‐coumaroyl‐α‐l ‐arabinofuranosyl)‐(1→5)‐l ‐arabinofuranose was isolated from the hydrolysate and identified by LC‐MS, GC‐MS, and NMR experiments. This study demonstrates for the first time that p‐coumaric acid can be linked to pectic side chains of dicotyledonous plants.     

Oxidative Cross-Linking of Pentosans by a Fungal Laccase and Horseradish Peroxidase: Mechanism of Linkage Between Feruloylated Arabinoxylans

The potential of a laccase from the fungus Pycnoporus cinnabarinus to cross-link feruloylated soluble wheat arabinoxylans was investigated using capillary viscometry, size-exclusion HPLC, and reverse-phase HPLC of phenolic compounds. The laccase results were compared with those for a hydrogen peroxide/horseradish peroxidase system. The oxidants provoked an increase in viscosity of a 0.2% (w/v) arabinoxylan solution. A gel was formed after 30 min with laccase. Hydrogen peroxide was consumed rapidly before a gel could be formed. Free ferulic acid, methyl ferulate, and vanillic acid inhibited the gelation, whereas fumaric acid had no effect. This suggests that the aromatic ring, and not the propenoic chain of ferulic acid, was the initiating site for arabinoxylan cross-linking. Ferulic acid and its 8-O-4′, 8-5′, and 5-5′ dehydrodimers were present in nonoxidized arabinoxylans. Upon oxidation, the 8-8′ and 8-5′ benzofuran dehydrodimers appeared and the 8-O-4′ and 8-5′ dimers increased. The production of dimers was proportional to the consumption of ester-bound ferulic acid. In cross-linked arabinoxylans, the major dimers were 8-5′ benzofuran, 8-8′, and 8-O-4′, whereas the 5-5′ dehydrodimer remained at the same level as in the nonoxidized solution.     

Effect of Holding Temperature on the Structures of Mung Bean Starch Gels and Noodles

The effect of storage temperatures (‐10, +1, and +10°C) on the structural organization of mung bean starch gels and noodles was studied by acid hydrolysis, X‐ray diffractometry, and gel‐permeation chromatography. The gels showed higher susceptibility to acid compared with the noodles as shown by the rate constants of the first stage of hydrolysis (k = 5.37–12.17 × 10^‐2/day and k = 4.19–4.61 × 10^‐2/day for gels and noodles, respectively). Acid hydrolysis showed no difference in the amount of resistant residues of both gels (42–46%) and noodles (44–45%), except for gels (38%) stored at ‐10°C. The acid‐resistant residues of both the gels and noodles had a B‐type X‐ray diffraction pattern (major reflections at 2θ = 19, 24, and 25°). The acid‐resistant residues of the unstored sample and those stored at ‐10°C for both gels and noodles contained chains with DP 46–54 and after debranching yielded two peaks with DP 29–39 and DP 15–19. The acid‐resistant residues of gels and noodles stored at +1 and +10°C contained chains with DP 35–37 and after debranching showed two chain populations with DP 31–33 and DP 14–19. These results indicate the greater participation of amylopectin in the retrogradation process occurring during storage at +1 and +10°C.     

Distribution of Total,Water‐Unextractable,and Water‐Extractable Arabinoxylans in Wheat Flour Mill Streams

Arabinoxylans are a minor but important constituent in wheat that affects bread quality, foam stability, batter viscosity, and sugar snap cookie diameter. Therefore, it is important to determine the distribution of arabinoxylans in flour mill streams to better formulate flour blends. Thirty‐one genetically pure grain lots representing six wheat classifications common to the western U.S. were milled on a Miag Multomat pilot mill, and 10 flour mill streams were collected from each. A two‐way ANOVA indicated that mill streams were a greater source of variation compared to grain lots for total arabinoxylans (TAX), water‐unextractable arabinoxylans (WUAX), and water‐extractable arabinoxylans (WEAX). TAX and WUAX were highly correlated with ash at r = 0.94 and r = 0.94, respectively; while the correlation for WEAX and ash decreased in magnitude at r = 0.60. However, the 5th middlings mill streams exhibited disparity between TAX and ash content as well as between WUAX and ash content. This may indicate that TAX and WUAX in mill streams are not always the result of bran contamination. Cumulative extraction curves for TAX, WUAX and WEAX revealed increasing gradients of arabinoxylans parallel to extraction rate. Therefore, arabinoxylans may be an indicator of flour refinement.     

Wheat Bran AX Properties and Choice of Xylanase Affect Enzymic Production of Wheat Bran‐Derived Arabinoxylan‐Oligosaccharides

Wheat bran‐derived arabinoxylan‐oligosaccharides (AXOS) recently have been shown to potentially exert prebiotic effects. In this study, 15 bran samples obtained by milling different wheat cultivars were treated with xylanases from Hypocrea jecorina (XHJ), Aspergillus aculeatus (XAA), and Pseudoalteromonas haloplanktis (XPH) to assess the effect of bran source and xylanase properties on the AXOS yield and structure. The total arabinoxylan (AX) extraction yield was higher with XHJ (8.2–10.7%) and XAA (8.2–10.8%) than with XPH (6.9–9.5%). Irrespective of the enzyme, a significant negative correlation was observed between extraction yield and arabinose to xylose (A/X) ratio of bran AX (r = –0.7), but not between yield and bran AX level. The A/X ratio of the extracted material was 0.27–0.34 for all bran samples and all enzymes, which combined with yield data and microscopic analysis, indicated primary hydrolysis of aleurone and nucellar epidermis AX. The average degree of polymerization (avDP) of the extracted AX was very low for all enzymes (2–3), owing to the release of high levels of monomeric arabinose and xylose. The release of these monosaccharides could be ascribed to 1) the activity of wheat bran‐associated enzymes (arabinofuranosidases and xylosidases); 2) the hydrolytic properties of the xylanases themselves; and 3) the presence of xylosidases as contaminations in enzyme preparation, in that order of importance. Heat treatment of bran before xylanase treatment significantly decreased the levels of monomeric arabinose and xylose in the extract, without affecting the extraction yield, resulting in a higher avDP of 3–7, thus yielding true AXOS. Overall, for AXOS production, wheat cultivars with a low bran A/X ratio of the AX are preferable as starting materials, and inactivation of bran‐associated enzymes before incubation is desirable. The XHJ xylanase was the best enzyme for wheat bran‐derived AXOS production.     

Distribution and Structural Variation of Nonstarch Polysaccharides in Milling Fractions of Hull‐less Barley with Variable Amylose Content

Three hull‐less barley genotypes containing starches with variable amylose content (23.8% normal, 4.3% waxy, 41.8% high‐amylose barley) were pearled to 10% and then roller‐milled to produce pearling by‐products (PBP), flour, and fiber‐rich fractions (FRF). PBP were enriched in arabinoxylans, protein, and ash and contained small amounts of starch and β‐glucans. FRF were considerably enriched in β‐glucans and arabinoxylans. The solubility of β‐glucans was higher in PBP than in FRF. The solubility of arabinoxylans was higher in FRF than in PBP. Small amounts of arabinogalactans detected in barley were concentrated in the outer portion of the barley kernel. The content and solubility of nonstarch polysaccharides (NSP) in various milling fractions was also dependent on the type of barley. To obtain more detailed information about the content and molecular structure of NSP, each milling fraction was sequentially extracted with water, alkaline [Ba(OH)₂], again with water, and finally with NaOH. These extractions resulted in four sub‐fractions: WE, Ba(OH)₂, Ba(OH)₂/H₂O, and NaOH. β‐Glucans and arabinoxylans exhibited structural heterogeneity derived from differences in their location within the kernel as well as from the genetic origin of barley. The WE arabinoxylans from FRF and flour had a substantially lower degree of branching than those from PBP. The WE arabinoxylans from FRF of high‐amylose and normal barley contained more unsubstituted Xylp residues but fewer doubly‐substituted and singly‐substituted Xylp at O‐2 than their counterparts from PBP. The WE arabinoxylans from FRF of waxy barley had a relatively high content of doubly‐substituted, but very few singly‐substituted Xylp residues. In all three barley genotypes, the ratio of tri‐ to tetrasaccharides in β‐glucans from PBP was higher than from flour and FRF. Substantial differences in the molecular weight of NSP in different milling fractions were also observed.     

Effects of nitrate‐, ammonium‐, and organic‐nitrogen‐based fertilizers on growth and yield of tomatoes

Mineral and organic fertilizers contain different forms and amounts of nitrogen (N), which can affect yield and product quality. The aim of this study was to determine appropriate amounts of N applied as nitrate (NO ), ammonium (NH ), and organic N (a mixture based on chicken manure) for optimal growth and quality of tomatoes. A pot experiment with sand as substrate was established in a greenhouse with six‐week‐old tomato plants (Lycopersicon esculentum Mill. cv. “Armada”). Nitrogen was applied in nutrient solutions at different NO : NH ratios combined with different chloride levels (NO ‐dominated, NO = NH at low Cl^–, NO = NH at high Cl^–, and NH ‐dominated, respectively) or as organic N at four N‐application rates (250, 500, 750, 1000 mg N plant^–1 week^–1). No significant differences in shoot biomass and yields of red tomatoes were observed between NO ‐ or NH ‐fed plants. Nitrogen rates above 750 mg N plant^–1 week^–1 did not significantly increase marketable fruit yield, but enhanced shoot‐biomass production. The NH ‐N‐dominated treatments (which also had high Cl^– concentrations) showed increasing incidence of blossom‐end‐rot (BER)‐infected fruits. In the organic‐N treatments, shoot‐biomass production and yields were lower than in the inorganic‐N treatments, but fruit quality was good with few BER‐infected fruits. The results show that with a total N supply below 750 mg N plant^–1 week^–1, NH can be used as equivalent N source to NO , resulting in equivalent yields of marketable fruit under the conditions in this experiment.     

Evaluation of N‐butyl phosphorothioic triamide for retardation of urea hydrolysis in soil

Abstract

Work reported showed that N‐butyl phosphorothioic triamide (NBPT) is considerably more effective than phenylphosphorodiamidate (PPD) as a soil urease inhibitor and merits consideration as a fertilizer amendment for retarding hydrolysis of urea fertilizer in soil. Studies to determine the factors influencing the effectiveness of NBPT for retardation of urea hydrolysis in soil showed that the inhibitory effect of NBPT on hydrolysis of urea by soil urease increased markedly with the amount of NBPT added and decreased markedly with time and with increase in temperature from 10 to 40°C. They also showed that the ability of NBPT to retard urea hydrolysis in 13 surface soils selected to obtain a wide range in properties was significantly correlated with organic C content (r = ‐0.70**), total N content (r = ‐0.76**), cation‐exchange capacity (r = ‐0.67* ), sand content (r = 0.61*), clay content (r = ‐0.63*), and surface area (r = ‐0.66*), but was not significantly correlated with pH, silt content, urease activity, or CaCO₃ equivalent. Multiple‐regression analyses indicated that the effectiveness of NBPT for retardation of urea hydrolysis in soil tends to increase with decrease in soil organic‐matter content.     

Effect of Food Additives on Deoxynivalenol (DON) Reduction and Quality Attributes in Steamed‐and‐Fried Instant Noodles

The effect of food additives reduction on quality attributes in steamed‐and‐fried instant noodles was investigated. Three additives, l ‐ascorbic acid, l ‐cysteine, and sodium bisulfite, were evaluated for their effect on deoxynivalenol (DON) reduction and sensory acceptability of instant noodles. After screening the different concentrations of three food additives, the maximum reduction of DON was optimized for the following concentration ranges: l ‐ascorbic acid, 0–100 μg/g; l ‐cysteine, 0–300 μg/g; and sodium bisulfite, 0–200 μg/g. The experimental results were fitted to a second‐order polynomial model, which gave a coefficient of determination (R²) of 0.987. The results indicated that the overall optimal condition resulting in the maximum DON reduction in instant noodles was obtained at the following combined level: sodium bisulfite, 167 μg/g; l ‐cysteine, 254 μg/g; and l ‐ascorbic acid, 23 μg/g. The sensory evaluation of noodles with the optimal condition of additives showed that the overall acceptability was in the range of “like slightly” and was not significantly (P > 0.05) different from the control sample. The optimized protocol produced a mixture that can reduce DON in instant noodles up to 67%. Modifying the processing of instant noodles by using additives may be useful to reduce the risk of DON exposure via instant noodles.     

Medium‐ and short‐term available organic matter,microbial biomass,and enzyme activities in soils under Pinus sylvestris L. and Robinia pseudoacacia L. in a sandy soil in NE Saxony,Germany

Total, mobile, and easily available C and N fractions, microbial biomass, and enzyme activities in a sandy soil under pine (Pinus sylvestris L.) and black locust (Robinia pseudoacacia L.) stands were investigated in a field study near Riesa, NE Germany. Samples of the organic layers (Oi and Oe‐Oa) and the mineral soil (0–5, 5–10, 10–20, and 10–30 cm) were taken in fall 1999 and analyzed for their contents of organic C and total N, hot‐water‐extractable organic C and N (HWC and HWN), KCl‐extractable organic C and N (C_org(KCl) and N_org(KCl)), NH ‐N and NO ‐N, microbial‐biomass C and N, and activities of β‐glucosidase and L‐asparaginase. With exception of the HWC, all investigated C and N pools showed a clear response to tilling, which was most pronounced in the Oi horizon. Compared to soils under pine, those under black locust had higher contents of medium‐ and short‐term available C (HWC, C_org(KCl)) and N (HWN, N_org(KCl)), mineral N (NH ‐N, NO ‐N), microbial‐biomass C and N, and enzyme activities in the uppermost horizons of the soil. The strong depth gradient found for all studied parameters was most pronounced in soils under black locust. Microbial‐biomass C and N and enzyme activities were closely related to the amounts of readily mineralizable organic C (HWC and C_org(KCl)). However, the presented results implicate a faster C and N turnover in the top‐soil layers under black locust caused by higher N‐input rates by symbiotic N₂ fixation.     

Isolation,Fractionation, and Structural Characteristics of Alkali‐Extractable β‐Glucan from Rye Whole Meal

The main nonstarch polysaccharide of rye is arabinoxylan (AX), but rye contains significant levels of (1→3)(1→4)‐β‐d ‐glucan, which unlike oat and barley β‐glucan, is not readily extracted by water, possibly because of entrapment within a matrix of AX cross‐linked by phenolics. This study continues objectives to improve understanding of factors controlling the physicochemical behavior of the cereal β‐glucans. Rye β‐glucan was extracted by 1.0N NaOH and increasing concentrations of ammonium sulfate were used to separate the β‐glucan from AX and prepare a series of eight narrow molecular weight (MW) distribution fractions. Composition and structural characteristics of the isolated β‐glucan and the eight fractions were determined. High‐performance size‐exclusion chromatography (HPSEC) with both specific calcofluor binding and a triple detection (light scattering, viscometry, and refractive index) system was used for MW determination. Lichenase digestion followed by high‐performance anion exchange chromatography of released oligosaccharides, was used for structural evaluation. The overall structure of all fractions was similar to that of barley β‐glucan.     

Relationship of Gelatinization and Recrystallization of Cross‐Linked Rice to Glass Transition Temperature

Nonwaxy rice starch was cross‐linked with sodium trimetaphosphate and sodium tripolyphosphate to obtain different degrees of cross‐linking (9.2, 26.2, and 29.2%). The objective was to investigate the influence of cross‐linking on thermal transitions of rice starch. Starch suspensions (67% moisture) were heated at 2°C/min using differential scanning calorimetry (DSC) to follow melting transition of amylopectin. Biphasic transitions were observed at ≈60–95°C in all samples. Melting endotherms of amylopectin shifted to a higher temperature (≤5°C) with an increasing degree of cross‐linking, while there was no dramatic change in enthalpy. Recrystallization during aging for 0–15 days was significantly suppressed by cross‐linking. The delayed gelatinization and retrogradation in crosslinked starch were evident due to restricted swelling and reduced hydration in starch granules. Glass transition temperature (T_g) measured from the derivative curve of heat flow was ‐3 to ‐4°C. No significant change in T_g was observed over the storage time studied.     

Isolation of an Antifungal Pathogenesis‐Related Protein from Naked Oat (Avena nuda) Seeds

A novel antifungal protein was isolated from naked oat (Avena nuda) seeds by acetone fractionation, (NH₄)₂SO₄ precipitation, Q‐Sepharose ion‐exchange chromatography, chitin affinity chromatography, and Sephacryl S‐200 gel filtration chromatography. The antifungal protein exhibited a molecular mass of 23,760, as measured by gel filtration and SDS‐PAGE. Matrix‐assisted laser desorption ionization–time of flight MS analysis indicated that the protein was homologous with a permatin precursor from A. sativa. The protein from naked oats exhibited antifungal activity against Trametes sp. SQ01 (half‐maximal inhibitory concentration [IC₅₀] = 5.68μM), Trichoderma spp. (IC₅₀ = 0.83μM), and Chaetomium sp. R01.     

Mutagenesis‐Derived Puroindoline Alleles in Triticum aestivum and Their Impacts on Milling and Bread Quality

Wheat (Triticum aestivum) end‐product quality is impacted by grain hardness, which is determined by the Hardness locus consisting of the Puroindoline a and Puroindoline b genes, Pina and Pinb, respectively. Hard wheats commonly contain just one of two Pin mutations. We previously demonstrated the creation and preliminary hardness testing of 46 Pin missense alleles. In this study we examine the degree that individual Pin missense alleles confer unique milling and bread quality traits. Three Pina (PINA‐R103K, ‐G47S, and ‐P35S) and four Pinb (PINB‐D34N, ‐T38I, ‐G46D, and ‐E51K) missense alleles were chosen because they impart variable grain hardness levels, with one allele conferring soft seed texture, three conferring intermediate hardness (single‐kernel characterization system [SKCS] hardness approximately 50), and three conferring hard grain texture (SKCS hardness greater than 60). All but two of the alleles (PINA‐R103K and PINA‐G47S) resulted in higher total flour yield when compared with wild‐type controls. All hard and intermediate hardness alleles had decreased break flour yield, but intermediate hardness allele PINA‐P35S had higher break flour yield than common hard allele Pinb‐D1b. Intermediate and hard alleles resulted in increased abundance of larger and reduced levels of smaller flour particles. None of the missense alleles differed from their controls for loaf volume. The seven selected Pin alleles imparted defined levels of grain hardness and milling properties not previously available that may prove useful in wheat improvement.     

REVIEW: Variability in Fine Structures of Noncellulosic Cell Wall Polysaccharides from Cereal Grains: Potential Importance in Human Health and Nutrition

Noncellulosic polysaccharides from the cell walls of cereal grains are not digested by human small intestinal enzymes and so contribute to total dietary fiber intake. These polysaccharides are becoming recognized increasingly for their potential to lower the risk of serious diet‐related conditions such as type II diabetes, cardiovascular disease, colorectal cancer, and diverticular disease. The effectiveness of noncellulosic cell wall polysaccharides in improving health outcomes is related to the fine structure and associated physicochemical properties. The two most nutritionally relevant wall polysaccharides of cereal grains are the arabinoxylans and the (1‐3,1‐4)‐β‐d ‐glucans. These polysaccharides have high molecular mass values but are nevertheless soluble in aqueous media, at least in part, where they adopt highly asymmetrical conformations and consequently form high viscosity solutions. Thus, arabinoxylans and (1‐3,1‐4)‐β‐d ‐glucans contribute to the soluble fiber component of human diets. The molecular size, solubility, and viscosity of the polysaccharides vary widely not only between different cereals but also within a single species. The variability in these properties reflects differences in the chemical structure of the polysaccharides, which in turn influences the beneficial effects of arabinoxylans and (1‐3,1‐4)‐β‐d ‐glucans in human diets. Here, we summarize information on the variability of fine structures of the arabinoxylans and (1‐3,1‐4)‐β‐d ‐glucans in common cereals and relate these to solubility, viscosity, and health benefits. The recent identification of genes involved in the biosynthesis of the (1‐3,1‐4)‐β‐d ‐glucans opens the way for the genetic improvement of cereal quality parameters that are important in human health.     

Composition and Regiodistribution of Fatty Acids in Triacylglycerols and Phospholipids from Red and Black Rices

Regiospecific profiles of fatty acids (FA) of triacylglycerols (TAG) and phospholipids (PL) isolated from red and black rices were investigated. The lipids extracted from red and black rices were separated by thin‐layer chromatography (TLC) into eight subfractions, respectively. With a few exceptions, the major lipid components were TAG (76.4–80.5%), free FA (7.2–9.8%), and phospholipids (3.5–3.6%), while hydrocarbons, steryl esters, diacylglycerols (1,3‐DAG and 1,2‐DAG), and monoacylglycerols were present in minor proportions (0.1–4.1%). The PL components isolated from the two cultivars were phosphatidyl choline (52.3–53.7%), phosphatidyl ethanolamine (22.3–23.1%), phosphatidyl inositol (20.6–21.3%), and others (<3.4%). No significant differences (P < 0.05) in FA distribution were found when these cultivars were compared. The principal characteristics of the FA distribution in the TAG and PL were evident in the rices between the two cultivars: unsaturated FA were predominantly located at the sn‐2 position (77.3–96.8%), while saturated FA primary occupied the sn‐1 or the sn‐3 position (35.0–78.7%) in these lipids. The results of this study could provide useful information to both consumers and producers during manufacture of traditional rice foods in Japan.