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     

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     

Xylitol bioproduction from wheat straw: hemicellulose hydrolysis and hydrolyzate fermentation

A 2² central composite design with five center points was performed to estimate the effects of temperature (120, 130 and 140 °C) and acid loading (100, 150 and 200 mg g^?1) on the yield of monomeric xylose recovery from wheat straw hemicellulose (Y_S/RM). Under the best hydrolysis condition (140 °C and 200 mg g^?1), a Y_S/RM of 0.26 g g^?1 was achieved. After vacuum concentration and detoxification by pH alteration and active charcoal adsorption, the hydrolyzate was used as source of xylose for xylitol bioproduction in a stirred tank reactor. A xylitol production of 30.8 g L^?1 was achieved after 54 h^?1 of fermentation, resulting in a productivity (Q_P) of 0.57 g L^?1 h^?1 and bioconversion yield (Y_P/S) of 0.88 g g^?1. The maximum specific rates of xylose consumption and xylitol production were 0.19 and 0.15 g g^?1 h^?1, respectively. Copyright © 2006 Society of Chemical Industry     

Revalorisation of vine trimming wastes using Lactobacillus acidophilus and Debaryomyces hansenii

BACKGROUND: Mild acid treatments of vine‐shoot trimmings result in the hydrolysis of hemicellulosic sugars that can be utilised by Lactobacillus acidophilus CECT‐4179 (ATCC 832) and Debaryomyces hansenii NRRL Y‐7426 as carbon sources to obtain food additives. Since the high content of glucose in these hydrolysates reduces the effective bioconversion of xylose into xylitol by D. hansenii, the use of Lactobacillus acidophilus, one of the main probiotic species, allows this problem to be solved by the selective consumption of glucose. In order to use both sugars (glucose and xylose), hemicellulosic vine‐shoot trimming hydrolysates can be sequentially fermented by both micro‐organisms. RESULTS: It was found that, in the first step, L. acidophilus generated almost exclusively lactic acid (32.7 g of lactic acid L^?1, Q_LA = 1.363 g L^?1 h^?1, Y_LA/S = 0.72 g g^?1) by homofermentative degradation of sugars (mainly glucose), and in the second step, the remaining hemicellulosic sugars were transformed primarily into xylitol by Debaryomyces hansenii (31.3 g of xylitol L^?1, Q_Xylitol = 0.708 g L^?1 h^?1, Y_Xylitol/S = 0.66 g g^?1). Furthermore, L. acidophilus proved to be a strong cell‐bounded biosurfactant producer. Cell extracts were able to reduce the surface tension (ST) of PBS in 18 mN m^?1 units. Lactobacillus acidophilus cells showed no difference in viability before or after PBS extraction of biosurfactants, achieving values of 0.9 × 10⁹ colony‐forming units (CFU) mL^?1 in both cases. CONCLUSIONS: These results have made a serious contribution to the re‐evaluation of a useless and pollutant residue, producing a wide range of natural food additives. Copyright © 2008 Society of Chemical Industry     

Phytosterol content in seven oat cultivars grown at three locations in Sweden

The total and individual sterol content in 21 oat samples (seven cultivars grown at three different locations in Sweden) were analysed by gas chromatography after acid hydrolysis. The total sterol content in these oat cultivars varied between 350–491 µg g⁻¹ of dry weight of kernel. The most abundant phytosterol was β‐sitosterol (237–321 µg g⁻¹) followed by campesterol (32–46 µg g⁻¹), Δ⁵‐avenasterol (15–47 µg g⁻¹) and stigmasterol (11–21 µg g⁻¹). There was a statistically significant difference in total sterol content between cultivars (p < 0.05) but no effect was found for cultivation location. Furthermore when contents of Δ⁵‐avenasterol in hexane‐extracted oat oil and acid‐hydrolysed oat samples were compared, it was noticed that the content of Δ⁵‐avenasterol was lowered due to acid hydrolysis. © 1999 Society of Chemical Industry     

Chemical composition,digestibility and protein quality of 12 sunflower (Helianthus annuus L) cultivars

Twelve sunflower (Helianthus annuus L) cultivars grown in Spain were analysed and tested in experiments with rats. The dehulled seeds contained an average of 32.2 MJ kg⁻¹ dry matter (DM) gross energy, 653 g kg⁻¹ DM fat, 60 g kg⁻¹ DM total non-starch polysaccharides (NSP) and 6 g kg⁻¹ DM Klason lignin. The sunflower seed hulls contained 20.2 MJ kg⁻¹ DM gross energy, 53 g kg⁻¹ DM fat, 562 g kg⁻¹ DM total NSPs and 239 g kg⁻¹ DM Klason lignin. The sunflower samples were dehulled and partially defatted (to ∼17% fat) and included in diets for rats. The dehulled, partially defatted samples contained on average 74.6 g nitrogen kg⁻¹ DM and 1.409 mg g⁻¹ phenolic compounds (chlorogenic acid + caffeic acid + derivative 1 + derivative 2) varying from 0.677 to 2.847 mg g⁻¹. Groups of five growing rats were fed diets (9.38% crude protein) containing one of the sunflower cultivars as the only source of protein. Apparent ileal and faecal digestibilities were determined by using an indigestible marker (Cr₂O₃) and faecal digestibility based on total faecal collections. Apparent ileal, caecal and faecal digestibilities of organic matter were 81.2–91.5% (P = 0.05), 95.8–97.1% (P = 0.005) and 94.7–95.3% (P = 0.94) respectively. The apparent faecal digestibilities of DM, energy and protein (N × 6.25) were 93.2–93.8%, 93.5–94.3% and 81.6–84.3% respectively with no differences among cultivars. Biological value (BV) ranged between 63.8 and 73.2% (P = 0.0001) and net protein utilisation (NPU) between 59.9 and 69.5% (P = 0.0001). BV and NPU were positively correlated with lysine and threonine contents, but no correlation with the analysed phenolic compounds was detected. © 1999 Society of Chemical Industry     

Evaluation of rheological properties,microstructure and water mobility in buns dough enriched in aleurone flour modified by enzyme combinations

This study aimed to explore the differences between single enzyme and combined enzymes in improving buns dough quality characterised by changes in rheological properties, microstructure and water mobility. The results indicated that xylanase (60 μg g⁻¹)–glucose oxidase (GOX) (40 μg g⁻¹) and xylanase (60 μg g⁻¹)–glucose oxidase (40 μg g⁻¹)–cellulase (30 μg g⁻¹)-modified dough can improve the negative effects of the single enzyme on the dough in terms of extensibility, tenacity and stability, leading to the formation of a softer gluten matrix. This may be due to xylanase (60 μg g⁻¹)–GOX (40 μg g⁻¹) and xylanase (60 μg g⁻¹)–GOX (40 μg g⁻¹)–cellulase (30 μg g⁻¹)-modified dough reduced the free sulfhydryl and significantly increased water-extractable arabinoxylan content (P < 0.05) and enhanced more less-tightly bound water availability. The microstructure observation showed that xylanase (60 μg g⁻¹)–GOX (40 μg g⁻¹) and xylanase (60 μg g⁻¹)–GOX (40 μg g⁻¹)–cellulase (30 μg g⁻¹) modified dough exhibited a more compact and continuous gluten matrix.     

Determination of anthocyanins,flavonoids and phenolic acids in potatoes. I: Coloured cultivars of Solanum tuberosum L

The major anthocyanins, flavonoids and phenolic acids in the tubers (skin and flesh), flowers and leaves of 26 cultivars of Solanum tuberosum L with coloured skins and/or flesh have been identified and quantified using analytical HPLC. Red tubers contained mostly pelagonidin-3-(p-coumaroyl-rutinoside)-5-glucoside (200–2000 μg g⁻¹ FW) plus lesser amounts of peonidin-3-(p-coumaroyl-rutinoside)-5-glucoside (20–400 μg g⁻¹ FW). Light to medium purple tubers contained petunidin-3-(p-coumaroyl-rutinoside)-5-glucoside (1000–2000 μg g⁻¹ FW) plus small amounts of malvidin-3-(p-coumaroyl-rutinoside)-5-glucoside (20–200 μg g⁻¹ FW) whilst dark purple–black tubers contained similar levels of petunidin-3-(p-coumaroyl-rutinoside)-5-glucoside together with much higher concentrations of malvidin-3-(p-coumaroyl-rutinoside)-5-glucoside (2000–5000 μg g⁻¹ FW). Tuber flesh also contained chlorogenic acid (30–900 μg g⁻¹ FW) and other phenolic acids plus low concentrations of flavonoids (0–30 μg g⁻¹ FW). Tuber skins showed much higher levels (1000–4000 μg g⁻¹ FW) of chlorogenic acid. The major anthocyanins in flowers were present as the rutinosides or other glycosides of pelargonidin, petunidin and malvidin whilst glycosides of cyanidin and delphinidin were found in some flowers, together with many of the same phenolic acids as found in tubers. The commonest flavonoids included rutin, kaempferol-3-rutinoside and two quercetin-rhamnose-glucosides. Flowers and leaves contained higher concentrations of flavonoids which fell into two patterns, with some cultivars containing high concentrations of quercetin-3-glycosides, whilst others had much lower concentrations. © 1998 SCI.     

Improving downstream processes to recover tartaric acid,tartrate and nutrients from vinasses and formulation of inexpensive fermentative broths for xylitol production

BACKGROUND: Vinasses, the main liquid wastes from the distillation process of grape marc and wine lees, are acidic effluents with high organic content, including acids, carbohydrates, phenols, and unsaturated compounds with high chemical oxygen demand, biological oxygen demand and solid concentrations. These wastes can be revalued to provide additional benefits when they are employed as feedstock of some compounds including tartaric acid, calcium tartrate and economic nutrients for the elaboration of fermentable broths. RESULT: This study attempts to recover tartaric acid and calcium tartrate from vinasses. All the tartaric acid initially solubilised was recovered in both processes. The residual streams can be successfully employed as economic nutrients for the xylose to xylitol bioconversion, achieving higher global volumetric productivities (Q_{P, xylitol} = 0.232 g L^?1 h^?1) and products yields (Y_xylitol/S = 0.57 g g^?1) than fermentations carried out using commercial nutrients (Q_{P, xylitol} = 0.193 g L^?1 h^?1 and Y_xylitol/S = 0.55 g g^?1 respectively). CONCLUSION: Tartaric acid can be recovered from vinasses in the form of tartaric acid crystals and calcium tartrate. The residual streams generated in the process can be used as economic nutrients for the production of xylitol by D. hansenii. Copyright © 2010 Society of Chemical Industry     

Characterisation of peptides in silages made from perennial ryegrass with different silage additives

The effects of applying either formic acid (5.4 g kg⁻¹), a mixture of formic acid (2.7 g kg⁻¹) and formaldehyde (1.5 g kg⁻¹, 81 g kg⁻¹ herbage crude protein) or two concentrations of a cysteine peptidase inhibitor, cystamine (5 or 50 g kg⁻¹), to perennial ryegrass (Lolium perenne) on the nitrogen (N) distribution of the resulting silages were investigated, with emphasis on changes in concentration, composition and molecular weight of silage peptides. Herbage (156 g dry matter kg⁻¹ and 141 g water‐soluble carbohydrate kg⁻¹ dry matter) was ensiled in triplicate in laboratory silos for 100 days. Formic acid and the formic acid/formaldehyde mixture reduced soluble non‐protein N and ammonia N concentrations (P < 0.01); in addition, formic acid increased peptide N concentrations (P < 0.05). Cystamine at 50 g kg⁻¹ reduced ammonia N concentrations (P < 0.01) and increased peptide N concentrations (P < 0.05), but when applied at 5 g kg⁻¹ had little effect. Gel filtration of silage extracts on Sephadex G‐25 suggested that a small proportion (0.06–0.11 g kg⁻¹ peptide N) of silage peptides had a chain length of 7–9 amino acids, but remaining peptides were smaller with chain lengths of 2–6 amino acid residues. Amino acid analysis of silage peptides indicated that additive treatment had little effect on peptide amino acid composition but that peptides with a chain length of 7–9 amino acids contained lower proportions of isoleucine and arginine. © 2000 Society of Chemical Industry     

Use of spent brewer's yeast in L‐(+) lactic acid fermentation

The application of by‐products from the brewing industry in lactic acid (LA) production was investigated in order to replace expensive nitrogen sources (such as yeast extract) with cheaper and renewable nitrogenous materials such as brewer's yeast (BY). In this study, brewer's spent grain (BSG) hydrolysate was used for L‐(+)‐LA fermentation by Lactobacillus rhamnosus ATCC 7469. The effect of pH control during the fermentation and the addition of various BY contents (5–50 g/L) in BSG hydrolysate on fermentation parameters was evaluated. BY addition significantly increased free amino nitrogen (FAN) concentration (by 25.2% at 5 g/L to 616% at 50 g/L). A strong positive correlation between FAN concentration in the hydrolysate and concentration of L‐(+)‐LA produced was observed (correlation coefficient of 0.913). A high cell viability of L. rhamnosus ATCC 7469 (1.95–3.32 × 10⁹ CFU/mL at the end of fermentation) was achieved in all fermentations with the addition of brewer's yeast. The addition of BY increased L‐(+)‐lactic acid yield and volumetric productivity up to 8.4% (5 g/L) and 48.3% (50 g/L). The highest L‐(+)‐LA yield (89%) and volumetric productivity (0.89 g/L h^?1) were achieved in fermentation of BSG hydrolysate with 50 g/L of BY. © 2019 The Institute of Brewing & Distilling     

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.     

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.     

Assessment of technological attributes of autochthonous starter cultures in Turkish dry fermented sausage (sucuk)

The study aims to evaluate the technological properties of autochthonous strains (Lactobacillus sakei S15, Lactobacillus plantarum S24, L. plantarum S91, Pediococcus pentosaceus S128b and Staphylococcus carnosus G109) in Turkish dry fermented sausage (sucuk). After 24 h of fermentaPtion, all lactic acid bacteria strains reduced the pH to below 5.0, while the pH in the control group was above 5.3. The number of lactic acid bacteria strains reached 10⁸–10⁹ cfu g⁻¹ during fermentation. Staphylococcus carnosus G109 remained at the inoculation level of 10⁶ cfu g⁻¹ during ripening. Lactobacillus sakei S15 as mono-culture showed higher TBARS values compared to other strains. The control group had the lowest L* value and autochthonous strains caused no significant difference for a* value. According to principal component analysis results, most volatile compounds were positively correlated with the group containing only L. sakei S15.     

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     

Influence of farmyard manure on the quality of grass silage

The influence of adding small aggregates (5 g) of farmyard manure (FYM) and/or a bacteria suspension (BS), containing Escherichia coli, and spores of Bacillus cereus and Clostridium tyrobutyricum, to silage was studied in two successive years. Direct cut (approximately 200 g DM kg⁻¹), precision-chopped grass herbage was ensiled in 1·6 l experimental silos. At ensiling the BS was either well distributed in the crop or added directly to 5 g of grass or FYM, which was placed in the centre of the green material when the silos were filled. Silage was further treated with formic acid (4 kg t⁻¹ FM), or an inoculant of lactic acid bacteria (10⁶ cfu g⁻¹ FM), and compared with no additive. Only minor influences on silage quality resulted from the addition of BS, although the number of clostridial spores increased slightly. Silages given additions of small aggregates of FYM were of poor quality. The inferior silage with a high number of clostridial spores (⩾3·9 cfu g⁻¹) and a high concentration of butyric acid (⩾2·8 g kg⁻¹) was found in the immediate vicinity of the addition. Application of silage additives did not improve silage quality. The poor quality of ‘FYM-silages’ could not solely be explained by the high number of organisms, but other factors in the manure and/or crops may contribute to the poor silage fermentation. © 1997 SCI.     

Chemical composition of the potential new oilseed crops Barbarea vulgaris,Barbarea verna and Lepidium campestre

Barbarea vulgaris, Barbarea verna and Lepidium campestre were selected as potential new oilseed crops. To evaluate the nutritional and technological quality of the seeds, the chemical composition was studied. The major constituents found were dietary fibre, crude fat and crude protein. Barbarea contained about 350 g kg⁻¹ dietary fibre, 295 g kg ⁻¹ crude fat and 170 g kg⁻¹ crude protein, while Lepidium contained about 400 g kg⁻¹ dietary fibre, 200 g kg⁻¹ crude fat and 190 g kg⁻¹ protein. The amino acid composition was found to be suitable for human consumption when comparison with the amino acid pattern for high quality protein was made. Fatty acid composition was dominated by erucic acid in B vulgaris (28%) and B verna (50%) and by linolenic acid in L campestre (34%). Insoluble dietary fibres were dominated by Klason lignin in both Barbarea and Lepidium. Uronic acid and glucose residues were also found in large amounts. Soluble dietary fibres were dominated by uronic acid, arabinose and galactose residues. The major glucosinolates found were glucobarbarin in B vulgaris (108 μmol g⁻¹), gluconasturtiin in B verna (106 μmol g⁻¹) and sinalbin in L campestre (110 μmol g⁻¹). No cyanogens were found in any of the seeds. © 1999 Society of Chemical Industry     

Effectiveness of organic acid,ozonated water and chlorine dippings on microbial reduction and storage quality of fresh‐cut iceberg lettuce

BACKGROUND: The comparative effects of organic (citric and lactic) acids, ozone and chlorine on the microbiological population and quality parameters of fresh-cut lettuce during storage were evaluated. RESULTS: Dipping of lettuce in 100 mg L⁻¹ chlorine solution reduced the numbers of mesophilic and psychrotrophic bacteria and Enterobacteriaceae by 1.7, 2.0 and 1.6 log₁₀ colony-forming units (CFU) g⁻¹ respectively. Treatment of lettuce with citric (5 g L⁻¹) and lactic (5 mL L⁻¹) acid solutions and ozonated water (4 mg L⁻¹) reduced the populations of mesophilic and psychrotrophic bacteria by 1.7 and 1.5 log₁₀ CFU g⁻¹ respectively. Organic acid dippings resulted in lower mesophilic and psychrotrophic counts than ozonated water and chlorine dippings during 12 days of storage. Lactic acid dipping effectively reduced (by 2.2 log₁₀ CFU g⁻¹) and maintained low populations of Enterobacteriaceae on lettuce for the first 6 days of storage. No significant (P > 0.05) changes were observed in the texture and moisture content of lettuce samples dipped in chlorine, organic acids and ozonated water during storage. Colour, β-carotene and vitamin C values of fresh-cut iceberg lettuce did not change significantly (P > 0.05) until day 8. CONCLUSION: Lactic and citric acid and ozonated water dippings could be alternative treatments to chlorine dipping to prolong the shelf life of fresh-cut iceberg lettuce. Copyright © 2007 Society of Chemical Industry     

Purification of angiotensin I-converting enzyme inhibitory peptides and antihypertensive effect of milk produced by protease-facilitated lactic fermentation

Fresh low-fat milk was fermented with five mixed lactic acid bacteria for up to 30 h at 42 °C. A protease, prozyme 6, was added 5 h after the beginning of fermentation. The whey was separated from the fermented milk and freeze-dried. As the fermentation time extended to 30 h, soluble protein content increased from 30.9 to 195.9 mg g⁻¹, free amino acid content increased from 2.8 to 192.8 mg g⁻¹, peptide content increased from 6.4 to 402.8 mg g⁻¹ and γ-aminobutyric acid (GABA) increased from 0 to 80.6 mg 100 g⁻¹, while inhibition of angiotensin I-converting enzyme (ACE) increased as indicated by a decrease of IC₅₀ from 1.18 to 0.24 mg mL⁻¹, respectively. The amino acid sequences of two ACE inhibitory peptides were Gly–Thr–Trp and Gly–Val–Trp, of which the IC₅₀ values were 464.4 and 240.0 μm, respectively. The systolic blood pressure and diastolic blood pressure of spontaneously hypertensive rat (SHR) were reduced 22 and 21.5 mm Hg, respectively, after 8 weeks of oral administration of diluted whey (peptide concentration 5 mg mL⁻¹) from the 30 h fermentation.     

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