The effect of sorbic acid on loss reduction during storage of orange peels

Sorbic acid (SA) at 0·25, 0·5 and 1·0 g kg^?1 was applied to fresh orange peels before ensiling in special 18 litre fermentation containers in two separate experiments. The higher two concentrations of sorbic acid were effective in reducing dry matter (DM) loss throughout the ensiling period, up to 90 days. Chemical analysis revealed that SA at the higher concentrations slowed down the fermentation rate, with less water-soluble carbohydrates (WSC) converted into organic acids and ethanol after 5 days of ensiling. However, after 30 and 90 days of ensiling, similar amounts of lactic acid were found in all silages, but less ethanol and more residual WSC were found in the silage treated with the higher SA concentrations. This indicates a more efficient fermentation pattern in the SA-treated silages. Microbial examination of the fresh and ensiled peels indicated large numbers of yeasts, the activity of which was probably inhibited by the sorbic acid.     

The effects of the rate of addition of formic acid and sulphuric acid on the ensilage of perennial ryegrass in laboratory silos

Perennial ryegrass was ensiled in laboratory silos after addition of formic acid (850 g kg^?1) or sulphuric acid (906 g kg^?1) at rates of 0, 2, 4 and 6 litres t^?1 fresh grass. Silos were opened after 6, 18 and 90 days and the silage subjected to chemical and microbiological analysis. The untreated control was poorly fermented with a final pH of 4.7, a butyric acid concentration of 19 g kg^?1 dry matter (DM) and an NH₃-N content of 275 g kg^?1 total nitrogen (TN). For the formic acid treatments the 2 litre t^?1 and 6 litre t^?1 levels both produced well-preserved silages but they were of different types. The silage treated with 2 litre t^?1 had a pH of 4.0, a lactic acid concentration of 92 g kg^?1 DM and 161 g NH₃-N kg^?1 TN, whereas with the 6 litre t^?1 treatment, fermentation had been severely restricted. The pH was 4.2, the lactic acid concentration was only 8 g kg^?1 DM and the NH₃-N content was 80 g kg^?1 TN. However, formic acid at 4 litre t^?1 produced a badly fermented silage of final pH 5.0 with lactic acid and butyric acid concentrations of 16 and 15 g kg^?1 DM, respectively, and an NH₃-N content of 149 g kg^?1 TN. Sulphuric acid at 2 and 4 litres t^?1 produced silages of low lactic acid contents, 36 and 24 g kg^?1 DM, and they also contained butyric acid in concentrations of 13 and 11 g kg^?1 DM; respective NH₃-N contents were 206 and 114 g kg^?1 DM. When sulphuric acid was added at 6 litres t^?1, despite a reduction in the pH of the grass to 3.5, fermentation was not restricted as it was with the equivalent level of formic acid. Lactic acid was present at 27 g kg^?1 DM and the ethanol concentration was very high at 66 g kg^?1 DM; the sulphuric acid-treated silages were characterised by high yeast counts. At the higher rates of addition, formic acid reduced the.     

Production of fermentable media from vine‐trimming wastes and bioconversion into lactic acid by Lactobacillus pentosus

Trimmings of vineshoots, an agricultural waste with little use, were hydrolysed with dilute sulphuric acid (1–5%) in order to obtain sugar solutions suitable as fermentation media. The operational conditions for hydrolysis were selected on the basis of both the generation of hemicellulosic sugars (mainly xylose) and glucose and the concentrations of reaction byproducts affecting fermentation (furfural, hydroxymethylfurfural and acetic acid). Hemicellulosic hydrolysates were supplemented with nutrients and fermented with Lactobacillus pentosus, without any previous detoxification stage, to produce lactic acid. Under the best operational conditions assayed (3% H₂SO₄ and 15 min), 21.8 g lactic acid l^?1 was produced (Q_P = 0.844 g l^?1 h^?1, Y_P/S = 0.77 g g^?1), which represents a theoretical yield of 99.6%. Acetic acid was the primary byproduct formed from xylose, at about 25% of the lactic acid level. Copyright © 2004 Society of Chemical Industry     

The occurrence and prevention of ethanol fermentation in high‐dry‐matter grass silage

Ethanol is a common, usually minor fermentation product in ensiled forages, the major product being lactic acid. Occasionally, high levels of ethanol are found in silages. The aim of this study was to determine the incidence of high‐dry‐matter (DM) grass silages containing ethanol as the main fermentation product (ethanol silages), to describe the fermentation process in such silages and to determine the effect of grass maceration prior to wilting and addition of a bacterial inoculant containing Lactobacillus plantarum and Enterococcus faecium strains on fermentation. Twenty‐one laboratory silages produced between 1993 and 1995, 21 farm silages produced between 1980 and 1989 and 36 farm silages produced in 1995 (all produced without additive) were examined for pH and chemical composition. Dry matter (DM) loss during ensilage was determined for the laboratory silages only. Four laboratory silages were identified as ethanol silages. Mean concentrations of ethanol, lactic acid and acetic acid were 48.1, 15.5 and 6.0 g kg⁻¹ DM respectively. In the silages that contained lactic acid as the main fermentation product (lactic acid silages) these values were 7.7, 45.5 and 15.1 g kg⁻¹ DM. Mean DM loss and pH were 62.8 g kg⁻¹ DM and 5.32 respectively for ethanol silages and 24.4 g kg⁻¹ DM and 4.69 for lactic acid silages. There was no difference between ethanol silages and lactic acid silages in the mean concentration of ammonia‐N (94 g kg⁻¹ total N), and butyric acid was not detected (<0.2 g kg⁻¹ DM), indicating that both types of silages were well preserved. Analysis of the composition of the grass at ensiling showed a positive correlation between the concentration of soluble carbohydrates and the development into ethanol silage. Analysis of the farm silages indicated that 29% of the silages produced between 1980 and 1989 and 14% of those produced in 1995 were ethanol silages. Maceration prior to wilting and addition of silage inoculant improved lactic acid fermentation and prevented high ethanol levels. The micro‐organisms responsible for ethanol fermentation as well as the implications of feeding ethanol silages to livestock remain to be resolved. © 2000 Society of Chemical Industry     

Comparative evaluation of laboratory-scale silages using standard glass jar silages or vacuum-packed model silages

BACKGROUND: The objective of this study was to compare the fermentation variables of laboratory‐scale silages made in glass preserving jars (GLASS) and vacuum‐packed plastic bags (Rostock model silages, ROMOS). Silages were prepared from perennial ryegrass (fresh and wilted, 151 g kg^?1 and 286 g kg^?1 dry matter (DM), respectively) and remoistened coarsely ground rye grain (650 g kg^?1 DM) either with or without the addition of a lactic acid bacteria inoculant (3 × 10⁵ colony forming units (cfu) g^?1, LAB). Quintuplicate silos were opened on days 2, 4, 8, 49 and 90. RESULTS: Silage pH (P = 0.073), acetic acid content (P = 0.608) and ethanol content (P = 0.223) were not influenced by the ensiling method. The contents of DM (P < 0.001) and propionic acid (P = 0.008) were affected by the ensiling method, but mean differences were only marginal. In ROMOS the concentration of lactic acid was increased (P = 0.007) whereas butyric acid was produced less (P = 0.001) when compared to GLASS. This suggested slightly better ensiling conditions for ROMOS. CONCLUSIONS: ROMOS represents a reasonable alternative to glass jar silages and opens the possibility for further investigations, e.g. studying the impact of packing density as well as the quantitative and qualitative analysis of fermentation gases. Copyright © 2010 Society of Chemical Industry     

Effects of harvest date, wilting and inoculation on yield and forage quality of ensiling safflower (Carthamus tinctorius L.) biomass

BACKGROUND: Safflower (Carthamus tinctorius L.), usually grown as a source of oil crop, can be used as fodder either for hay or ensiling purposes, particularly in semi‐arid regions. RESULTS: A 2‐year trial was conducted in southern Italy to evaluate the production and forage quality of safflower biomass cv. Centennial, harvested at three different stages: 1, at complete appearance of primary buds (PB); 2, at complete appearance of secondary and tertiary buds (STB); and 3, at 25% of flowering stage (FS). For each stage of growth, 50% of the biomass was ensiled in 4 L glass jars without and with inoculation (Lactobacillus plantarum, LAB), and the other 50% was field wilted for 24 h before ensiling. Dry matter (DM) content and yield (DMY), pH, buffering capacity (BC) and water soluble carbohydrates (WSC) were determined on fresh forage. On safflower silages were also evaluated ammonia‐N, crude protein (CP), fibre fractions, fat, lactic and acetic acids, Ca and P, and gas losses. DMY ranged from 4.5 t ha^?1 (PB harvesting) to 11.6 t ha^?1 (FS harvesting). DM content varied from 129 g kg^?1 (PB not wilted) to 630 g kg^?1 (FS wilted). The WSC in forage before ensiling with not wilting ranged from 128 (PB stage) to 105 and 100 g kg^?1 DM at STB and FS stages, respectively. The wilted safflower forage showed a lower WSC compared to wilted forage. The high sugar substrate allowed lactic acid fermentation and a good conservation quality in all the harvesting stages. Silages quality was strongly influenced by the treatment performed. Wilting practice increased DM, pH and NDF contents but reduced lactic acid, acetic acid and NH₃‐N values. Inoculation reduced DM, pH and NDF contents, but increased lactic and acetic acids, CP and ash. CONCLUSION: As result, wilting the forage for 1 day was very effective in the early harvesting stage because this practice significantly increased DM, reducing on the same time the intensive fermentation and proteolysis processes of silage. When harvesting is performed at the beginning of the flowering stage wilting is not necessary. Copyright © 2011 Society of Chemical Industry     

Variation in short chain fatty acid and ethanol concentration resulting from the natural fermentation of wheat and barley for inclusion in liquid diets for pigs

Fifty‐six samples of wheat and 44 samples of barley were taken, at harvest, from locations across the UK. Lactic acid bacteria (LAB) and yeasts were enumerated before the samples were ground. Following grinding, triplicate 30‐g samples of each cereal were mixed with sterile distilled water and incubated at 30, 35 or 40 °C. Samples were taken immediately after mixing and at 24‐h intervals for analysis of short‐chain fatty acids (SCFA) and ethanol by isocratic ion‐exclusion liquid chromatography. The number of LAB and yeasts present in samples ranged from 0 to 5.0 (mean 2.25 ± 1.31) and 3.30 to 6.25 (mean 4.96 ± 0.74) log₁₀ colony‐forming units (cfu) ml^?1 respectively. At 30 °C the mean concentrations (mmol l^?1) of SCFAs and ethanol were, lactic acid 59.6 ± 40.0 (range 0.14–134.9), acetic acid 23.2 ± 11.1 (range 2.9–51.4), butyric acid 17.2 ± 16.8 (range 0.0–62.2) and ethanol 15.0 ± 9.0 (range 4.6–53.7) respectively. After fermentation for 24 h only 9 of 300 fermentations produced more than 75 mmol l^?1 lactic acid, which has previously been demonstrated to prevent the growth of Salmonella in liquid pig feed. Fermenting at 35 or 40 °C had no effect on lactic acid concentration but significantly (p < 0.001) increased the concentrations of acetic and butyric acids and ethanol. These results indicate that natural fermentation cannot be relied upon to produce levels of SCFAs that will prevent the proliferation of enteropathogens. Copyright © 2004 Society of Chemical Industry     

Modelling of the hydrolysis of sorghum straw at atmospheric pressure

Sorghum straw is a renewable, cheap and widespread resource. The acid hydrolysis of sorghum straw to obtain xylose solutions could be a good alternative for this abundant resource. The H₂SO₄ hydrolysis of sorghum straw at two different temperatures (80 and 100 °C) and three H₂SO₄ concentrations (2, 4 and 6%) using a solid/liquid ratio of 1:10 (w/w) was studied. Kinetic parameters of mathematical models for predicting the concentrations of xylose, glucose, acetic acid and furfural were determined. The activation energy of the release reaction was 183.3 kJ mol^?1 for xylose and 185.8 kJ mol^?1 for glucose. The optimal conditions found were 6% H₂SO₄ at 100 °C for 60 min, which allow one to obtain a solution with 18.27 g xylose l^?1, 6.78 g glucose l^?1, 0.7 g furfural l^?1 and 1.35 g acetic acid l^?1. It is concluded that this process has potential for utilisation of this renewable lignocellulosic resource. © 2002 Society of Chemical Industry     

Enhanced lactic acid fermentation of silage by the addition of green tea waste

The effects of green tea waste (GTW) addition on the ensiling of forage were investigated. Wet and dried GTW added at 10, 50, 100 and 200 g kg^?1 of fresh matter (FM) and at 2, 10 and 20 g kg^?1 FM, respectively, decreased pH and increased lactic acid concentration of the silages, whereas the butyric acid concentration and ammonia nitrogen content, as a proportion of a total nitrogen, were lowered, compared with silage without additives (control). To investigate the effect of GTW‐associated LAB on silage fermentation, wet GTW was sterilized by autoclaving or gamma irradiation and added at 50 g kg^?1 FM. The silages made with sterilized GTW showed higher lactic acid concentrations, and lower pH and butyric acid concentrations than controls. The counts of lactic acid bacteria (LAB) were higher in silages made with sterilized GTW than control until 10 days after ensiling. The enhanced lactic acid fermentation was not found when green tea polyphenols (GTP) were added. These data suggested that GTW could enhance LAB growth and lactic acid production of silage, particularly when added at 50 g kg^?1 FM in a wet form or at the equivalent in a dry form. Although neither GTW‐associated LAB nor GTP accounted for the enhancement of lactic acid fermentation, GTW would possibly supply some nutrients which are heat‐stable and effective for LAB growth during silage fermentation. Copyright © 2004 Society of Chemical Industry     

Fermentation characteristics,aerobic stability and ruminal degradation of ensiled pea/wheat bi‐crop forages treated with two microbial inoculants,formic acid or quebracho tannins

This study evaluated the effects of two commonly used microbial inoculants (Lactobacillus buchneri (LB) and Lactobacillus plantarum (LP)), formic acid (FA) and quebracho tannins (QT) on the fermentation quality, aerobic stability and in situ rumen degradation of pea/wheat bi‐crop forages. Precision‐chopped spring pea (Pisum sativum, var Magnus) and wheat (Triticum aestivum, var Axona) bi‐crops (3:1 pea/wheat ratio) harvested at a combined dry matter (DM) content of 301 g kg^?1 were used for the study. The bi‐crops were conserved without (Control) or with inoculants based on lactic acid bacteria (LB (10⁵ CFU g^?1 fresh weight (FW)) or LP (10⁶ CFU g^?1 FW)), QT (16 g kg^?1 FW) or FA (2.5 g kg^?1 FW) in laboratory silos of 1.5 kg capacity, with each treatment being replicated six times. The pH, chemical composition, aerobic stability and in situ rumen degradation of DM, nitrogen (N) and neutral detergent fibre (NDF) after 112 days of ensilage were measured. The average pH at silo opening was 4.0, suggesting that the silages were well fermented. There were no significant effects of additive treatment on water‐soluble carbohydrate, total N, soluble N, ammonia N and NDF. Lactic acid and acetic acid were the main fermentation products. High concentrations of acetic acid were found in all the treatments, indicating a heterofermentative pathway. Although FA treatment gave the most aerobically stable silage, the Control and QT‐treated silages did not heat up by more than 1 °C until after 6 days of exposure to air. There were no effects of additives on DM degradation characteristics. However, the inoculants increased the rate of N and NDF degradation in the rumen, and both FA and QT reduced the effective and potential degradation of N. © 2001 Society of Chemical Industry     

Cellulase and Bacterial Inoculant Effects on Cocksfoot and Lucerne Ensiled at High Dry Matter Levels

Limited information exists on the response of grass and legume silage to enzyme and bacterial inoculant treatments when wilted to drier than desired conditions. This study was undertaken to evaluate the impact of cellulase (from Trichoderma longibrachiatum) application rate, when combined with a bacterial inoculant (Lactobacillus plantarum and Pediococcus cerevisiae), on the fermentation characteristics of cocksfoot (Dactylis glomerata L) and lucerne (Medicago sativa L) ensiled at high dry-matter concentrations. Forages were wilted to near 600 g dry matter kg^-1 and cellulase, combined with inoculant, was applied at 0·30 ml kg^-1 herbage and at two, four and eight times this concentration (at least 2500 IU ml^-1). Cellulase was also applied alone at 0·60 ml kg^-1. Wilted forages were ensiled in laboratory silos for 60 days. Effect of cellulase application rate on neutral detergent fibre concentrations of the silages was small and inconsistent. Averaged across species, only the intermediate cellulase concentrations decreased neutral detergent fibre concentration (P=0·082). The limited cell-wall degradation was probably related to the high silage dry-matter and lignin concentrations. Cellulase combined with inoculant increased total fermentation, when averaged across species. In cocksfoot, cellulase combined with inoculant decreased pH and NH₃-N concentration but increased the lactic: acetic acid ratio of control silage, with most of the effect caused by the inoculant. Cellulase applied alone to lucerne caused a higher lactic: acetic acid ratio than the control or when combined with the inoculant at the same cellulase rate. Thus, the effect of cellulase–inoculant mixtures on silage quality varied among plant species, with cocksfoot generally more responsive than lucerne. © 1997 SCI.     

Effects of Silage Fermentation and Post-ruminal Casein Supplementation in Lactating Dairy Cows: 1—Diet Digestion and Milk Production

Two silages were prepared from the first-cut sward of timothy-meadow fescue and wilted to a dry matter (DM) content of 300 g kg^-1. One was ensiled with the addition of a formic-acid-based additive (4 litres formic acid (FA) per tonne) and the other with the addition of a bacterial inoculant (LAB) at a rate of 5×10⁶ colony forming units g^-1. Both silages were well preserved, but the extent of fermentation was greater in LAB-silage than in FA-silage as indicated by a lower concentration of water soluble carbohydrates (68 vs 177 g kg^-1 DM) and a higher concentration of lactic acid (147 vs 32 g kg^-1 DM). Four Ayrshire cows were used in a 4×4 Latin square experiment with 21-day periods to study the effects of silage fermentation and postruminal casein supplementation on silage intake, nutrient supply and milk production. The four treatments were FA-silage without casein (FA-0), LAB-silage without casein (LAB-0), FA-silage with casein (FA-C) and LAB-silage with casein (LAB-C). Both silages were given ad libitum with 8 kg day^-1 of barley without or with 400 g day^-1 of casein infused into the duodenum. Organic matter digestibility was lower (0·723 vs 0·753; P<0·01) for FA-silage than for LAB-silage. Cows offered FA-silage had a higher molar proportion of acetate and a lower proportion of propionate in ruminal fluid than cows offered LAB-silage. Microbial protein synthesis estimated from the output of purine derivatives in urine was greater (288 vs 260 g N day^-1; P<0·05) for cows given FA-silage compared with LAB-silage. Feeding LAB-treated silage tended (P<0·10) to decrease silage DM intake compared with FA-treated silage (10·61 vs 11·77 kg DM day^-1). Silage composition did not affect significantly milk yield or milk composition. Casein infusion increased milk yield (25·1 vs 27·1 kg day^-1; P<0·05), milk protein content (32·4 vs 33·8 g kg^-1; P<0·05) and protein yield (808 vs 905 g day^-1; P<0·01). The responses were similar for both silages. © 1997 SCI.     

Production of detoxified sorghum straw hydrolysates for fermentative purposes

Sorghum straw can be hydrolysed to obtain monosaccharide solutions, mainly containing xylose. The usual biotechnological application of xylose is its bioconversion to xylitol. The global process from straw to xylitol can give an added value to the sorghum straw. The process has the following sequential steps: reduction of size, acid hydrolysis, neutralization, detoxification, fermentation, recovery and purification. This work deals with the optimization of the detoxification process of sorghum straw hydrolysates with activated charcoal. The variables evaluated were pH (1–5), contact time (20–60 min) and activated charcoal charge (20–33 g kg^?1). Mathematical models were obtained through a factorial experimental design. The models suggest that optimal conditions for detoxification are pH 1, contact time of 29 min and a charcoal charge of 33 g kg^?1. These conditions allowed hydrolysates with 54.2 g xylose L^?1, 13.5 g glucose L^?1, 12 g arabinose L^?1, 0.2 g furfural L^?1 and 0.0 g acetic acid L^?1 to be obtained. The results suggest that performing the detoxification step before the neutralization step gave the best outcome. Fermentations by Candida parapsilosis NRRL Y‐2315 were performed and it was confirmed that the treated hydrolysate is suitable for xylitol production, yielding up to 17 g L^?1 of this polyol. Copyright © 2006 Society of Chemical Industry     

Simultaneous lactic acid and xylitol production from vine trimming wastes

Hemicellulosic hydrolyzates from vineshoot trimmings obtained by dilute sulfuric acid hydrolysis were evaluated for xylitol production by Debaryomyces hansenii NRRL Y‐7426. Bioconversion was not efficient, however, since a mixture of products (mainly ethanol) was achieved. Taking into account that hexoses (such as glucose or mannose) can inhibit xylose metabolism by repression and inactivation of the xylose transport system or catabolic enzymes and that these hemicellulosic hydrolyzates are characterized by a high glucose concentration, a novel technology was developed, sequentially transforming glucose into lactic acid by Lactobacillus rhamnosus followed by fermentation of xylose into xylitol by Debaryomyces hansenii after L. rhamnosus removal by microfiltration. Optimal conditions were achieved using detoxified concentrated hemicellulosic hydrolyzates, after CaCO₃ addition in both stages of fermentation and using nitrogen purges after sampling in order to reduce the oxygen dissolved. Under these conditions 31.5 g lactic acid L^?1 (Q_LA = 1.312 g L^?1 h^?1 and Y_LA/S = 0.93 g g^?1) and 27.5 g xylitol L^?1 (Q_Xylitol = 0.458 g L^?1 h^?1 and Y_Xylitol/S = 0.53 g g^?1) were produced. Finally, lactic acid was selectively recovered using the resin Amberlite IRA 400 (0.0374 g of lactic acid g^?1 of dry resin), allowing a further recovery of xylitol by sequential stages of adsorption, concentration, ethanol precipitation, concentration and crystallization to obtain food‐grade xylitol according to a developed process. Copyright © 2007 Society of Chemical Industry     

Biodegradation of cell wall components of maize stover colonized by white-rot fungi and resulting impact on in-vitro digestibility

Treatment of crop residues with some species of white-rot fungi can enhance digestibility. This study was conducted to investigate changes in in-vitro dry matter disappearance (IVDMD) and degradation of cell wall constituents in maize (Zea maize L) stover treated with three white-rot fungi: Cyathus stercoreus, Phlebia brevispora and Phanerochaete chrysosporium. Solid fermentation of maize stover for 28 days at 27°C improved IVDMD from 409 g kg^?1 (control) to 514 g kg^?1 for P brevispora and 523 g kg^?1 for C stercoreus. In contrast, growth of P chrysosporium reduced IVDMD from 409 to 298 g kg^?1. All fungi degraded cell wall p-coumaric acid (PCA) and ferulic acid (FA), but P chrysosporium was the least effective in degrading PCA and FA. Conversely, P chrysosporium degraded lignin 1·6 times more effectively than C stercoreus and 1·4 times more than P brevispora, indicating that lignin degradation alone cannot account for the IVDMD enhancement and that degradation of PCA and FA may be important. Hemicelluloses were preferentially and highly utilized by all the fungi. Cellulose was extensively degraded only by P chrysosporium (69% lost after 28 days of incubation), while substrate colonized by the other two fungi retained more than 84% original cellulose. Incubation of C stercoreus and P brevispora decreased the concentrations of both xylose and arabinose, but increased glucose concentration, whereas P chrysosporium removed less xylose and decreased glucose concentration. Preferential removal of arabinose over xylose by the fungi caused an increase in the xylose to arabinose ratio of the treated residues. Enhanced digestibility may have resulted from cleavage of lignin-carbohydrate bonds. Results of this study suggest that digestibility enhancement of maize stover colonized by white-rot fungi is regulated by a complex combination of various factors, including the degradation of structural carbohydrates, cell wall phenolic acids and lignin.     

Influence of Fermentation Time and an ‘Indigenous Tenderiser’ (Kanwa) on the Microbial Profile,Chemical Attributes and Shelf-Life of Rice Masa (a Nigerian Fermented Product)

Investigations on the influence of fermentation time, ‘Kanwa’ (an indigenous tenderiser and a flavouring agent) and potassium sorbate (0·5, 1·0 or 1·5 g kg⁻¹) were conducted by examining the microbial profile, chemical attributes and shelf-life of rice ‘Masa’ (a Nigerian fermented product). Various types of microorganisms occurred at the initial stages of rice slurry fermentation and these included fungi (Aspergillus spp, Penicillium spp, Saccharomyces spp, Rhizopus spp) and bacteria (Lactic acid bacteria, Bacillus spp, Enterobacter spp and Acetobacter spp). But beyond 8 h fermentation time, fewer types of micro-organisms (Lactobacillus spp, Saccharomyces spp and Rhizopus spp) were isolated.Total aerobic counts increased significantly (P=0·05) as fermentation progressed (0, 6 or 12 h), with lactic acid bacteria (LAB) and yeasts dominating and probably contributed to the sour–sweet spongy characteristic of the rice Masa. But after fermentation and baking process, the rice Masa became dominatedand spoilt by Bacillus spp, Lactobacillus spp and Saccharomyces spp withstorage time. Longer fermentation time resulted in a less acceptable product,being more acidic. Rice Masa produced from a 6 h fermentation showedbetter sensory qualities (aroma and visual appearance). Use of Kanwa(Na₂CO₃.NaHCO₃.2H₂O) improved aroma but was detrimental to visualappearance and spoilage was accelerated, probably due to higher pH. Potassium sorbate at higher concentrations (1·0 and 1·5 g kg⁻¹) induced beneficial antimicrobial effects and reduced the microbial load thereby prolonging the shelf life of the rice Masa (treated with 1·5 g kg⁻¹) by about 3 days.     

Evaluation of fermentation and aerobic stability of wet brewers' grains ensiled alone or in combination with various feeds as a total mixed ration

Wet brewer's grains (BG; 200 g kg^?1 dry matter(DM)) were ensiled alone or in combination with various dry feeds as a total mixed ration (TMR; 540 g kg^?1 DM) in laboratory silos. Ensilage was stopped at 40 days (experiment 1) or at 5, 20, 40 and 60 days (experiment 2) after storage. The composition of soluble sugars and the profiles of fermentation products were determined. The 60 day silages were subjected to aerobic deterioration and changes in silage temperature were recorded for 7 days. A rapid pH fall coupled with accelerated lactic acid production was observed in BG silage; soluble sugars, mainly composed of maltose and raffinose, completely disappeared within 5 days of ensiling. Prolonged storage, however, decreased lactic acid concentration and increased acetic acid greatly. Appreciable amounts of propionic acid and 1‐propanol were also produced in BG silage in the late stages of fermentation. When TMR silage was made, the decline in pH and the increase in lactic acid were delayed due to the low moisture content. Acetic acid production was enhanced from the beginning of storage, and mannitol accumulated in TMR silage. Yeast numbers were lower in TMR than in BG silage, but the changes were limited in the late stages of fermentation. When exposed to air, the temperature of BG silage increased after 3 days, whereas that of TMR silage appeared stable during the 7 days test. The results indicate that BG is a suitable by‐product for ensiling and, when ensiled with various feeds as a TMR, improved stability against aerobic deterioration can be expected. Copyright © 2003 Society of Chemical Industry     

Non-conventional fermentation at laboratory scale of cocoa beans: Using probiotic microorganisms and substitution of mucilage by fruit pulps

In a non-conventional lab-scale fermentation of cocoa beans using probiotic microorganisms and substituting the cocoa pulp for fruit pulp, physicochemical, microbiological and quality parameters were investigated. Two hundred grams of beans were fermented in a controlled environmental chamber (temperature ramp rate of 25°C for 48 h; 35°C for 48 h and 45°C for 48 h; and 65% HR). pH, titratable acid, citric, lactic and acetic acids, as well as sugars and ethanol were measured. A cut test was also performed on the cocoa beans fermented 5 and 6 days. As the fermentation time progressed, citric acid concentration decreased until 0.53 g kg⁻¹, whereas both lactic and acetic acids increased until 0.44 and 16.58 g kg⁻¹, respectively. Sucrose content decreased from 12.26 g kg⁻¹ (in fresh) to 6.54 g kg⁻¹ on the 6th day. Fructose and glucose contents increased in the cotyledons from day five, reaching a maximum concentration of 1.14 and 1.01 g kg⁻¹, respectively, on day six. Yeasts were the main microorganisms during the first 24–48 h (8.4 log CFU g⁻¹), while bacterial counts reached its highest number (7.8 log CFU g⁻¹) on day four. Beans fermented 5 and 6 days resulted in more fermented beans (>81%) and less violet ones (<18.4%) than the control.     

Increase in low molecular size uronic acid in ripening banana fruit

Uronic acid soluble in ethanol/water (4:1 v/v) increased from 9 ± 1 mg kg^?1 fresh weight in pulp of unripe banana fruit. Musa (AAA Group, Cavendish subgroup) ‘Williams’, to 53 ± 13 mg kg^?1 fresh weight in fruit ripened for 13 days. This increase began within the first 2 days of ripening. Uronic acid soluble in phenol/acetic acid/water (2:1:1 w/v/v) increased from 15 ± 5 to 86 ± 17 mg kg^?1 fresh weight during the first 8 days of ripening, accompanied by a decrease in cell wall uronic acid from 10·2 ± 0·8 to 4·4 ± 0·4 g kg^?1 fresh weight. Most or all of the uronic acid in extracts of ripe pulp cochromatographed with monogalacturonic acid. The results were consistent with hydrolysis of cell wall polyuronides by exopolygalacturonase (EC 3.2.1.67).     

Seasonal Changes in the Composition and Properties of a High Dietary Fibre Powder from Grapefruit Peel

Seasonal changes in composition and properties of a high dietary fibre product from grapefruit peel were studied. Total dietary fibre decreased in January as compared to September (586–686 g kg^-1). Main constituents from soluble fibre were: uronic acids (172–233 g kg^-1), arabinose (13–41 g kg^-1), galactose (4–11 g kg^-1), glucose (5–10 g kg^-1) and xylose (2–3 g kg^-1). Insoluble dietary fibre (385–392 g kg^-1) did not significantly change during the season. Its main constituents were: Klason lignin (29–37 g kg^-1), uronic acids (33–70 g kg^-1) and neutral sugars: glucose (149–196 g kg^-1), mannose (45–50 g kg^-1), xylose (25–38 g kg^-1), galactose (20–22 g kg^-1) and arabinose (16–45 g kg^-1). Total neutral sugars from dietary fibre decreased over the harvest period (315–383 g kg^-1) and an inverse trend was observed in total free-sugars from samples (49–85 g kg^-1). Both, water holding capacity (7·0–9·3 g water g^-1 dry sample) and glucose retardation index (7·0–25·3%) decreased from early stages in fruit development until late in the harvest season. Seasonal changes in grapefruit peel should be taken into account, in order to standardise the quality of rich fibre products. © 1997 SCI