Characterisation of Odorous Compounds and Emissions from Slurries Produced from Weaner Pigs Fed Dry Feed and Liquid Diets

Changes in odorous emissions were recorded from slurries produced by weaner pigs fed dry feed and feed with water added in the respective ratios of 3:1 and 4:1. Slurries were placed in an environmentally controlled emissions chamber, periodic air sampling was performed to determine the olfactometric response as odour concentration, and the air was analysed to identify volatile organic compounds present. Distinctive odours were produced by each slurry. However, four major groups of odorants were identified as sulphides, volatile fatty acids, phenols and indoles. The odour concentration from the slurry of the 4:1 diet was significantly less (P<0·05) than the odour concentration from the dry feed and 3:1 slurry samples. Decay of the sulphide component of the odours was investigated and the role of methanogenesis in reducing odour production is discussed. While monitoring the emissions in the chamber the slurry odorant concentrations increased by up to 50 ppm h^-1. © 1997 SCI.     

A novel technique to determine organic processes in pig wastes

Complex processes concerning declining concentration of organic matter within pig wastes have been investigated using deuterated phenol (d₅) and acetic acid (d ₄) over a ten day period. Decomposition rates of products responsible for odours and pollution were also quantified. These products included the volatile fatty acids, phenols and indoles as well as gaseous methane and carbon dioxide. The last two were quantified in the headspace flow to assess methanogenesis and the activity of bacteria. The relative rates of emission, production and bio‐decay were calculated as exponential curves showing that acetic acid was lost through emission and bio‐decay with half lives of 158 h and 95 h, respectively. Bio‐production of acetic acid was very low. The emission rate of methane was 4.0 g m ⁻³ d⁻¹. The ratio of methane generated to the bio‐decay of acetic acid concentration was 1: 66. The decline of acetic acid in slurry was shown to be a concentration‐dependent process. Other volatile fatty acids demonstrated similar declining concentration characteristics but at a lesser rate. This was also the case for 4‐methyl phenol with a half life of 495 h. However phenol demonstrated different declining concentration and production characteristics with a maximum concentration of 85 mg l⁻¹ at 175 h. Carbon dioxide was produced at a greater rate than acetic acid was lost from the slurry (a ratio of 1.88: 1.0). Ammonia was emitted at a rate of 4.7 g m⁻² d⁻¹. © 1999 Society of Chemical Industry     

High carbon dioxide pressure inactivation kinetics of Escherichia coli in broth

The inactivation kinetics of Escherichia coli by high pressure carbon dioxide was investigated. Inactivation rates increased with increasing pressure (25, 50, 75 and 100 atm), temperature, and exposure time. Microbial inactivation followed first order reaction kinetics, with inactivation rates (k) and decimal reduction times (D) that varied from 0·0848 to 0·4717 min⁻¹and from 4·90 to 27·46 min, respectively, at treatment temperatures (20, 30 and 40°C). The inactivation rates of E. coli were described by the apparent activation volume (ΔV^*) and a ‘pressure z value’, and they were greatly dependent on both temperature and pressure.     

Evaluation of the influence of mastication on temporal aroma release of ripe and unripe bananas,using a model mouth system and gas chromatography-olfactometry

The effect of the mastication rate on temporal aroma release from ripe and unripe bananas was investigated using a model mouth system and analysing the volatiles by gas chromatography-olfactometry (GC-O) and gas chromatography-mass spectrometry. Large differences were found in the numbers of odour active compounds of ripe and unripe bananas as well as for the three different mastication rates investigated (0, 26 and 52 min^-1). Hexanal was the only compound that was detected by all six assessors for ripe and unripe bananas for each mastication speed. In the odour profile of ripe and unripe bananas with a mastication rate of 52 min^-1, 18 and 7 significant odour active compounds respectively were detected whereas with a mastication rate of 26 min^-1, 15 and 3 respectively were detected. Without mastication only 3 and 2 compounds respectively were observed. Principal component analysis on GC-O data allowed an easy separation between the three chewing speeds and the ripe and unripe bananas.     

Determination of Chlorogenic Acids with Lactones in Roasted Coffee

An HPLC method has been developed which allowed the determination of mono- and dicaffeoylquinic acids (CQA and di-CQA), corresponding lactones (CQL) and feruloylquinic acids (FQA) in roasted coffee within one chromatographic run. The elution order was verified by isolation of the individual compounds by preparative HPLC, chromatography of the fractions on the analytical HPLC system, NMR spectroscopy and thermospray LC-MS. At least 15 additional minor compounds had the spectra of hydroxycinnamic acids, some of them only occurring in roasted coffee. Caffeoyltryptophan, which has been identified some time ago by another working group could also be separated with this system. The average contents in commercial roasted coffee samples (n=12) were: 3-CQA, 5·0 g kg⁻¹; 4-CQA, 6·2 g kg⁻¹; 5-CQA, 11·4 g kg⁻¹; 4-FQA, 0·7 g kg⁻¹; 5-FQA, 1·4 g kg⁻¹; 3-CQL, 2·1 g kg⁻¹; 4-CQL, 1·0 g kg⁻¹; 3,4-di-CQA, 0·7 g kg⁻¹; 3,5-di-CQA, 0·4 g kg⁻¹ and 4,5-di-CQA, 0·8 g kg⁻¹ dry matter. There were only small differences between the different brands. Two series of samples with different degrees of roast produced from the same green coffee have also been analysed. One series was steam treated before roasting (a process which is commercially used to improve digestibility). Only in the initial stages of roasting (light roast) could a difference in the contents of the acids between both series be observed. Keeping coffee brews at an elevated temperature (4 h at 80°C) reduced the amounts of CQL to 60% of the initial value. The contents of 3-CQA and 4-CQA increased, whilst that of 5-CQA decreased. The overall contents of CQA decreased.     

Deacetylated chitin used as adsorbent in production of clarified pineapple syrup

A study of clarification of pineapple wastes syrup by a combined process of membrane ultrafiltration (UF), ion exchange and adsorption techniques using partially deacetylated chitin (PDC) as adsorbent material was conducted. Chitin from Black Tiger shrimp shell was used after undergoing deproteination, demineralisation and deacetylation with different concentrations of sodium hydroxide (NaOH). The performance of cation resin (Dowex 88), anion resin (Dowex 66) and PDC as adsorbent material were evaluated. Effects of flow rate ranging from 10 to 50 ml min⁻¹ on operation and regeneration of the resins were also investigated. Chitin yield was about 31·2% of the shrimp shells, corresponding to about 89% recovery of the total chitin content of the shells. When treated with 5%, 10%, 20% and 30% NaOH, the degree of deacetylation increased with increasing concentration of sodium hydroxide. In ion exchange process, cation resin removed more than 90% of K⁺, Mg²⁺ and Ca²⁺ from UF mill juice at a flow rate of 30 ml min⁻¹. In adsorption process, anion resin (Dowex 66) had more colorant removed (94% T) from UF mill juice than PDC treated with 30% NaOH (84·4% T). The optimum flow rate for cation resin was 10 ml min⁻¹ for both operation and regeneration while for PDC, 30 ml min⁻¹ was optimum for operation and 10 ml min⁻¹ for regeneration. The concentrated pineapple syrup was clear with a colour value of 70·2% and pH value of 4·96. The main reducing sugars after concentration were glucose, fructose and sucrose at 29·05, 15·72 and 18·62% (w/v), respectively. © 1998 SCI.     

Nonenzymatic Browning in Pear Juice Concentrate at Elevated Temperatures

The effect of temperature and soluble solids (°Brix) on nonenzymatic browning in pear juice concentrate was determined by following absorbance at 420 nm (A₄₂₀) over the temperature range of 50–80°C. Browning could be modeled as a zero order rate process with rates of 22.2 × 10⁻⁴ (45.2 °Brix), 36.9 × 10⁻⁴ (55.4 °Brix), 53.5 × 10⁻⁴ (65.1 °Brix) and 107 × 10⁻⁴ (72.5 °Brix) A₄₂₀· min⁻¹ at 80°C. Temperature dependence was described by the Arrhenius relationship with an average activation energy of 21.9 kcal · mole⁻¹. Formol titration indicated a 20% loss of amino acids during heating 4.4 hr at 80°C and no loss of carbohydrates was observed after any heating period.     

Nutrient contents,rumen protein degradability and antinutritional factors in some colour- and white-flowering cultivars of Vicia faba beans

Six colour-flowering (Scirocco, Alfred, Carola, Condor, Tina and Herz Freya) and six white-flowering (Caspar, Albatros, Gloria, Tyrol, Vasco and Cresta) cultivars of Vicia faba were studied. The crude protein contents of colour- and white-flowering cultivars were 267±13·6 and 283±18·8 g kg⁻¹, respectively, which did not differ significantly at P<0·05. The levels of lipids, crude fibre, starch and ash varied from 14 to 22 g kg⁻¹, 88 to 143 g kg⁻¹, 407 to 485 g kg⁻¹ and 32 to 42 g kg⁻¹, respectively. The calculated organic matter digestibility (OMD) and metabolisable energy (ME) of the white-flowering cultivars were significantly higher (P<0·001) than those of the colour-flowering cultivars (OMD: 889·1±26·6 g kg⁻¹ vs 797·5±17·1 g kg⁻¹; ME: 13·97±0·49 vs 12·30±0·34 MJ kg⁻¹). In all cultivars, sulphur amino acids were lower than adequate concentration when compared with recommended amino acid pattern of FAO/WHO/UNO reference protein for a 2–5-year-old child. The in vitro rumen nitrogen degradability of colour-flowering cultivars was significantly lower (P<0·01) compared to that of white-flowering cultivars (71·4±9·3% vs 88·0±11·1%). Amongst colour-flowering varieties, the contents of total phenols (TP), tannins (T) and condensed tannins (CT) were highest in Alfred (28·3, 21·0 and 35·4 g kg⁻¹, respectively). The contents of TP and T were similar (about 15 and 10 g kg⁻¹, respectively) in Carola, Tina and Herz Freya, and the CT were in the order: Condor>Herz Freya>Carola. The CT were not detected in white-flowering varieties, T were virtually absent and TP were extremely low (4·0–4·9 g kg⁻¹). The activities of other antinutritional factors (white- and colour-flowering cultivars, respectively: trypsin inhibitor activity 3·05±0·34 and 1·85±0·09 mg trypsin inhibited g⁻¹; lectin 27·2±9·4 and 27·1±5·1 mg ml⁻¹ assay medium producing haemagglutination; phytate 15·0±2·7 and 16·6±2·3 g kg⁻¹) were very low. A strong negative correlation (r=-0·92, P<0·001) between tannins and in vitro rumen protein degradability was observed which suggested that tannins have adverse effect on protein degradability. Similarly negative correlations between tannin levels and metabolisable energy (r=-0·89; P<0·001) and organic matter digestibility (r=-0·89; P<0·001) were observed. The correlation coefficient between trypsin inhibitor activity and tannins was negative and highly significant (r=-0·88, P<0·001), whereas between tannins and saponins it was significantly positive (r=0·96, P<0·001). ©1997 SCI     

Hardaliye: fermented grape juice as a traditional Turkish beverage

Twenty-six aged hardaliye samples, collected from different spots of the Kirklareli province of Turkey and hardaliye produced in laboratory conditions using the traditional method were investigated in this study. The pH ranged from 3·21 to 3·97. Red colour (Hunter Lab a_Lvalue) of samples ranged from 1·33 to 9·66. The total bacterial count ranged from 3·5×10²to 8×10⁵cfu ml⁻¹. The lactic acid bacteria counts of the samples were found to be between 1·0×10²and 4·0×10⁴cfu ml⁻¹. Yeasts and moulds, which were found in 21 samples out of 26, ranged from 1·0×10²to 8·1×10⁴cfu ml⁻¹. Coliforms and Escherichia coli were found in none of the samples. The changes of some microbiological and chemical properties of hardaliye during fermentation were investigated. The pH of hardaliye dropped from 3·86 to 3·39. The ethanol content of the end product was determined as 595·50 mg dl⁻¹. During the fermentation process, the total bacteria count, lactic acid bacteria count and yeast count changed from 2·1×10⁵, 6·0×10⁴and 1·2×10⁵cfu ml⁻¹to 1·3×10², 1·2×10³and 1·1×10³cfu ml⁻¹, respectively.Lactobacilli isolated from hardaliye samples were characterized by API 50 CH and other phenotypic criteria. A succession of Lactobacillus species, dominated by L. paracasei subsp. paracasei and L. casei subsp. pseudoplantarum were found during the fermentation process.     

Effects of intraruminal infusions of propionate and butyrate with two different protein supplements on milk production and blood metabolites in dairy cows receiving grass silage-based diet

Four cows were used in a balanced 4×4 Latin square with 2 week experimental periods to investigate the effects of intraruminal infusions of volatile fatty acids and protein source on milk production and blood metabolites. The four treatments in a 2×2 factorial arrangement were isoenergetic intraruminal infusions of propionate (500 g day⁻¹) or butyrate (417 g day⁻¹) each given with isonitrogenous protein supplementation of fish meal (FM) or barley protein (BP). The cows were fed restrictively with 9 kg dry matter day⁻¹ of formic acid treated grass silage and 8 kg day⁻¹ of concentrate. Propionate infusion increased milk yield (24·9 vs 23·4 kg day⁻¹; P<0·05), milk protein yield (832 vs 778 g day⁻¹; P=0·05) and milk lactose content (44·7 vs 43·5 g kg⁻¹; P<0·05) and yield (1113 vs 1023 g day⁻¹; P<0·01), whereas butyrate infusion was associated with a higher milk fat content (44·7 vs 39·4 g kg⁻¹; P<0·01) and yield (1033 vs 974 g day⁻¹; P<0·01). FM tended (P<0·10) to increase milk yield, but had no significant effects on milk composition or milk component yields compared with BP. Butyrate infusion increased blood ketones, plasma non-esterified fatty acids and glycine relative to propionate infusion. The concentrations of ammonia N in rumen fluid and urea in plasma and milk were similar for both protein supplements. The profile of amino acids in plasma was similar for both protein supplements except for the higher concentrations of phenylalanine, proline and tyrosine with BP. The results show that protein utilisation can be improved by increasing the supply of propionate from rumen fermentation in cows given a grass silage-based diet. © 1998 SCI.     

Injury,Inhibition and Inactivation ofEscherichia coli O157:H7 by Potassium Sorbate and Sodium Nitrite as Affected by pH and Temperature

The effect of potassium sorbate (0–2 g litre⁻¹) and sodium nitrite (0–1 g litre⁻¹) on the growth of four strains of Escherichia coli O157: H7 in tryptic soya broth at various pH levels (pH 4·0–7·0 for sorbate, pH 5·0–8·0 for nitrite) were determined at 37°C and 4°C. Among the pH levels tested, sorbate and nitrite exhibited the highest antimicrobial activity at pH 4·0 and 5·0, respectively. At pH 5·0 and 37°C, the presence of 500 mg litre⁻¹ sorbate or 200 mg litre⁻¹ nitrite completely inhibited the growth of E coli O157: H7. While at higher pH levels, 2 g litre⁻¹ sorbate or 1 g litre⁻¹, nitrite, the highest concentration tested, did not show significant antimicrobial action against the test organisms. At 4°C and pH 5·0, the inoculated test organisms did not showed any significant growth in preservative-free control media. Different degree of inactivation and injury was observed when E coli O157: H7 strain 933 was stored in TSB (pH 5·0) containing 1 g litre⁻¹ sorbate or nitrite at 37°C. At 4°C, inactivation and injury of E coli O157: H7 cells was not observed in the medium containing sorbate or nitrite throughout the 24 h experimental period.     

In vitro biohydrogenation and total tract digestibility of oleamide by sheep

Disappearance of cis-18:1(n-9) from ruminal in vitro cultures supplemented with either oleic acid or oleamide was measured over 48 h to determine if the amide resisted biohydrogenation. Oleamide added to the substrate maintained higher concentrations of cis-18: 1(n-9) in the microbial cultures at 24 and 48 h of incubation compared to substrates with added oleic acid. Disappearance rates of cis-18: 1(n-9) from the cultures, which were calculated as a measure of biohydrogenation, were 0·064 and 0·025 h⁻¹ for the oleic acid and oleamide supplements, respectively. Four sheep were fed four diets (control, 42 g kg⁻¹ oleic acid, 23 g kg⁻¹ oleamide, and 45 g kg⁻¹ oleamide) in a 4×4 Latin square to determine how the amide affected fatty acid digestibility. Total tract digestibilities of protein and fibre were not affected (P>0·05) by either oleic acid or oleamide compared to the control diet. Fatty acid and energy digestibilities were not changed (P>0·05) by oleic acid, but were increased (P<0·05) when oleamide was added to the sheep diets at 45 g kg⁻¹. These results show that oleamide resists ruminal biohydrogenation without impairing fatty acid digestibility. © 1998 SCI.     

Isolation and characteristics of yeasts able to grow at low concentrations of nutrients

Seven oligotrophic yeasts, which can grow in a 10⁴-fold dilution of malt–yeast–glucose–peptone medium (10⁻⁴ YM), were mainly isolated from soil. These yeasts belong to the Cryptococcaceae. When inoculated at about 10² cells/ml in 10⁻⁴ YM, the isolates grew to 1·4×10³–2·4×10⁵ cells/ml after 3 days. Some culture collection yeasts fell into three groups according to their growth characteristics in 10⁻⁴ YM, one group showing characteristics of the oligotrophic yeasts. The half-saturation values of uptake by the five isolated oligotrophic yeasts for D-glucose, L-leucine and L-amino acids were 6·0–25·0, 1·7–43·3 and 3·5–21·6 μM, respectively. The oligotrophic yeasts suspended in 10 mM-phosphate buffer (pH 6·0) had high tolerances for starvation, and remained more than 15% viable after 90 days of starvation. © 1998 John Wiley & Sons, Ltd.     

Proofing of bread dough assisted by ohmic heating

Proofing of bread dough was studied under ohmic heating for a target temperature of 35°C. An experimental device based on PLC monitoring was developed to study the effect of heating rates and voltages on the proofing process. Conventional and ohmic heating-assisted proofing were compared; the results showed that the process itself had no impact on the proofing when identical heating rates (0.065°C·min^− 1) were used. However, increasing the heating rate could significantly reduce the time needed to reach an expansion ratio of 3 (from 122 min during conventional proofing to 65–70 min during ohmic heating in the range of 1–10°C·min^− 1). This was due to the shortening of the lag phase at the beginning of proofing (from 58 min during conventional heating to 20 min at 10°C·min^− 1 in ohmic heating). Results also showed that the voltage intensity had no significant effect on the proofing kinetics in the range of 50–150 V. The evolution of expansion ratios with proofing time could be fitted by a Gompertz model with a very high accuracy (R² > 0.999)     

In vitro protein digestibility and mineral availability of green beans (Phaseolus vulgarisL) as influenced by variety and pod size

Three varieties of green beans (Cleo, Strike and Sentry) were harvested and sorted into four fractions according to pod size (diameter <7 mm; 7–8·5 mm; 8·6–10 mm and >10 mm). Ash content and dietary fibre increased significantly as pod size increased mainly in Cleo and Strike beans. Strike showed the highest fibre content (378·0 g kg⁻¹) but the lowest carbohydrate (364·6 g kg⁻¹) and ash (68·4 g kg⁻¹) values. Mean values for Fe and Mg content were higher in Cleo beans (70·9 and 27·1 mg kg⁻¹, respectively), Zn, Cu and Mg were higher in Strike beans (48·7 mg kg⁻¹, 22·4 mg kg⁻¹ and 3·15 g kg⁻¹, respectively) while Na and Ca values were maximum in Sentry (459·1 mg kg⁻¹ and 7·11 g kg⁻¹, respectively). Trypsin inhibitor was negatively related to in vitro protein digestibility but no relationship was found between this last parameter and phytic acid content. This antinutrient, together with dietary fibre, and a negative influence on in vitro mineral dialysability of green beans. © 1998 SCI     

Response of pancreatic secretions to feeding diets with low and high levels of soybean trypsin inhibitors in growing pigs

Studies were carried out to determine the effect of soybean trypsin inhibitors (SBTI) on exocrine pancreatic secretions in growing pigs. Six barrows with an average initial body weight (BW) of 27·1±1·4 kg were fitted with permanent pancreatic re-entrant cannulas and fed two diets according to a crossover design. Two maize starch-based diets were formulated to contain 200 g kg⁻¹ crude protein from either Nutrisoy (food grade defatted soy flour) or autoclaved Nutrisoy. The concentrations of SBTI in Nutrisoy and autoclaved Nutrisoy diets were 13·4 and 3·0 g kg⁻¹, respectively. The experiment consisted of two periods of 9 days each. The average BW at the start of the first and second experimental periods was 33·5±2·7 and 37·2±3·7 kg, respectively. The average BW at the conclusion of the experiment was 41·8±3·9 kg. The volume of pancreatic secretion was higher (P<0·01) when the Nutrisoy, as opposed to the autoclaved Nutrisoy diet was fed (3804 vs 2634 ml (24 h)⁻¹). The concen-tration of nitrogen and protein and specific activities (units litre⁻¹) of amylase, chymotrypsin and trypsin were lower (P<0·05) in pancreatic juice of pigs fed the Nutrisoy diet. There were no differences (P>0·05) in the total secretions of nitrogen (g (24 h)⁻¹) and total activities (units (24 h)⁻¹) of amylase, lipase, chymotrypsin and trypsin in pancreatic juice of pigs fed the Nutrisoy and autoclaved Nutrisoy diets. However, the total secretion of protein was slightly higher (25·7 vs 22·8 g (24 h)⁻¹; P<0·05) in pancreatic juice of pigs fed the autoclaved Nutrisoy diet, which corresponded with the increase in the secretion of protein-bound amino acids. There was also an increase in the total secretion of free amino acids in pancreatic juice. These studies show no effect of SBTI on the total enzyme activities in pancreatic juice of growing pigs. © 1998 SCI.     

Effects of sodium and potassium fertilisers on the composition of herbage and its acceptability to dairy cows

Fertilisation of herbage with Na can increase acceptability to cows, but the influence of fertiliser rate and fertilisation by K is unknown. In experiment 1, ten cows were grazed on pasture plots that had just been fertilised with 0–132 kg-Na ha⁻¹ (current Na) and had received 0–64 kg-Na ha⁻¹ in the previous grazing season (residual Na). Herbage Na concentration increased in proportion to current Na from 2·7 to 4·9 g-Na kg⁻¹ dry matter (DM) and also increased with increasing residual Na from 2·2 to 4·5 g-Na kg⁻¹ DM. Herbage K concentrations were low (10 g kg⁻¹ DM at 0 kg-Na ha⁻¹) and were only slightly reduced by Na fertiliser. Herbage Mg and Ca concentrations and DM digestibility were maximum at 66–99 kg-current-Na ha⁻¹. Cows grazed current-Na-fertilised plots to a lower height and spent more time grazing them. In experiment 2, pasture plots received no fertiliser, low and high isomolar and independent applications of Na and K or a combination of the two. The herbage was more mature than in experiment 1 and Na concentration of the herbage without Na fertilizer was high (5 g kg⁻¹ DM). Na fertiliser, therefore, only slightly increased Na concentration, more in clover than in grass, and had little effect on K concentration. K fertiliser increased K concentration from 16 to 20 g kg⁻¹ DM and reduced Na concentration to 3·5 g kg⁻¹ DM. Sodium fertiliser, therefore, only increased the acceptability of herbage to cattle when herbage Na concentrations were initially low (less than 5 g kg⁻¹ DM) and were increased substantially by the application of the fertiliser. © 1998 SCI.     

Oven drying improves the nutritional value of Calliandra calothyrsus and Gliricidia sepium as supplements for sheep given low-quality straw

Leaves from the tree legumes Gliricidia (Gliricidia sepium) and Calliandra (Calliandra calothyrsus) were fed as supplements (200 g dry matter) to sheep (n=3) given a basal diet of barley straw ad libitum. Tree leaves were fed either freshly harvested (F=fresh) or after drying at 60°C in a forced draught oven (D=dried). Voluntary intakes, digestibility and aspects of nitrogen (N) and phenolic compound metabolism were measured in all sheep. Drying decreased the condensed tannin (CT) content of Calliandra (F 117, D 82 g CT kg⁻¹ DM). Total phenolics (TP) were significantly decreased when Gliricidia was dried (F 39, D 21 g TP kg⁻¹ DM), and CT content was reduced from 20 g CT kg⁻¹ DM to zero. Sheep given Gliricidia had higher rumen ammonia concentrations (73–85 mg N litre⁻¹) than did sheep given Calliandra (37–40 mg N litre⁻¹). For both species, drying significantly increased the voluntary consumption of straw, increased DM digestibility, decreased faecal N excretion and increased N balance. For calliandra, drying decreased the apparent degradability of N in the rumen (DNR) from 0·40 to 0·28 g N g⁻¹ N ingested, and increased the apparent digestibility of N (ADN) in the post-ruminal tract from 0·20 to 0·52 g N absorbed g⁻¹ N flowing into the small intestines. For Gliricidia, DNR decreased from 0·64 to 0·51 and ADN increased from 0·41 to 0·56. There were no significant effects of drying on rates of microbial N synthesis. The above changes were discussed in relation to changes in tannin content and it was concluded that drying facilitates the formation of protein–tannin complexes which protect proteins from degradation in the rumen. These proteins are subsequently released in the small intestines, thereby promoting an increased efficiency of dietary N utilisation. ©1997 SCI     

Freeze-drying in a fluidized-bed atmospheric dryer and in a vacuum dryer: Evaluation of external transfer coefficients

The factors which influence freeze-drying are classified as either internal or external. Internal factors derive from the properties of the material undergoing drying, while external factors relate to the physical conditions under which drying occurs. This paper looks at the external factors and compares them for two different freeze-drying methods: a vacuum dryer and an atmospheric fluidized-bed dryer containing an adsorbent.First, the ratio between the external heat and mass transfer coefficients, h/K, was evaluated: this ratio for the fluidized-bed dryer was constant at 398·8 kcal torr kg⁻¹ °C⁻¹ but varied for the vacuum dryer within the range 9·5 to 16·2 kcal torr kg⁻¹ °C⁻¹. The individual heat and mass transfer coefficients were calculated. The mass transfer coefficient, K, for the vacuum dryer was 1·0 kg h⁻¹ m⁻² torr⁻¹; for the atmospheric fluidized-bed dryer, K varied slightly with temperature, being 0·7, 0·8 and 1·0 kg h⁻¹ m⁻² torr⁻¹, at fluidized-bed temperatures of 0, −10 and −20°C, respectively. At these temperatures, the heat transfer coefficients for the fluidized-bed dryer were 287, 321 and 402 kcal h⁻¹ m⁻² °C⁻¹, respectively. For the vacuum dryer h was 9·5–16·2 kcal h⁻¹ m⁻² °C⁻¹. Thus, K values were comparable in the two drying systems but h in the fluidized-bed dryer was some 20–40 times greater than in the vacuum dryer.The study helped to elucidate the mechanisms involved during ice sublimation and contributed towards developing a means by which freeze-drying patterns could be predicted. The results were helpful in providing guidelines during the development of the novel atmospheric fluidized-bed technique.     

Mathematical model for Phaffia rhodozyma growth using peat hydrolysates as substrate

The potential of peat hydrolysates for the production of astaxanthin from Phaffia rhodozyma yeast biomass in continuous fermentation was studied. Chemostat fermentations of the yeast were performed using peat hydrolysates as substrate. Kinetic parameters were calculated for the growth of the yeast and the biomass productivity was determined using mathematical models. A low maximum specific growth rate (μ_max=0·08 h⁻¹) and a high Monod constant (Ks=26·2×10³) were obtained for this substrate. The low maintenance energy requirement found, 0·020 g (gh)⁻¹, confirms the aerobic metabolism of the yeast with this substrate. Under selected conditions, a biomass productivity of 0·108 g (lh)⁻¹ and an astaxanthin productivity of 0·046 mg (lh)⁻¹ were obtained. The biomass produced had a high protein and astaxanthin content (490±8 g kg⁻¹ and 0.43±0.07 g kg⁻¹, respectively), indicating that it can be used as a feed additive. © 1998 SCI.