The immediate effect of gamma irradiation upon the sugar content of potatoes previously stored at 2, 4.5, 6, 10 and 15.5°C

Summary The sugar content of samples of potatoes, cv. Majestic, was varied by storage for 4 weeks at 2, 4.5, 6, 10 and 15.5°C, before irradiation with 10 krad. With initial sucrose contents of 0.14–0.37% FW (tubers from 4.5–15.5°C) the marked temporary increase in sucrose, as reported previously, was observed, reaching a maximum after 3–7 days before falling rapidly to a level rather higher than in non-irradiated tubers. Tubers from 2°C, with 1.4% sucrose, showed an immediate drop in this after irradiation, succeeded within 3 days by a rise to values not significantly different from the controls. Irradiation caused a significant increase in reducing sugar content, for a period of up to 7 days in sweetened tubers, but for 21 days or more in unsweetened tubers. Previous storage at the different temperatures had some permanent residual effect upon the sugar content of the controls during subsequent storage for up to 90 days at 10°C.     

Evaluation of treatments with hot water,chemicals and ventilated containers to reduce microbial spoilage in irradiated potatoes

Summary Potatoes irradiated to control sprouting were dipped in: hot water (56°C, 5 min; 52°C, 10, 15 and 20 min); cold (25°C, 5 min) or hot (56°C, 5 min) salicylic acid (1000 and 2000 ppm); or sodium hypochlorite (0.1 and 0.2%, 5 min); or dusted with salicylic acid (1 and 2%), to try to reduce the incidence of bacterial soft rot (Erwinia sp.) during controlled temperature (10°C, 15°C) and ambient temperature (20–34°C) storage. All treatments, particularly hot water and hot salicylic acid dip, increased microbial spoilage, possibly as a result of handling damage during the treatments combined with the inhibition of wound periderm formation as a result of irradiation. Storing irradiated tubers in well ventilated containers reduced soft rot compared to storing them in sacks and after 6 months storage at 10, 15 and 20–34°C, 95, 90 and 77% respectively were healthy and marketable.     

Amylolytic activity in stored potato tubers. 2. The effect of low-temperature storage on the activities of α-and β-amylase and α-glucosidase in potato tubers

Summary Tubers of the potato cultivars Record, Wilja, Pentland Dell and Brodick (formerly clone 137371) were sampled before and after storage at either 4°C or 10°C. Reducing sugar content stayed constant during storage at 10°C in all four cultivars but rose greatly during the first 6–12 weeks of storage at 4°C in Record, Wilja and Pentland Dell but not in Brodick. Amylolytic activity was determined after 5 weeks storage using blockedp-nitrophenyl maltoheptaoside as substrate for α-amylase,p-nitrophenyl maltopentaoside as substrate for β-amylase, andp-nitrophenylglucopyranoside as substrate for α-glucosidase. The values obtained from tubers stored at 4°C were higher than those from tubers stored at 10°C, the differences being much less in Brodick than in the other three cultivars.     

Post-harvest characteristics of potato minitubers with different fresh weights and from different harvests. II. Losses during storage

Summary Storage losses were studied in minitubers of cvs Agria and Liseta, using five fresh weight classes (<0.50 g, 0.5–0.99 g, 1.00–1.99 g, 2.00–2.99 g, ≥3.00 g), and three successive harvests of the same plantlets. After each harvest, tubers were dired at room temperature (1 day), curred at 18 °C (13 days) and stored at 2 °C (540 days). Two kinds of storage losses were considered: (a) losses of entire tubers because of deterioration, and (b) fresh weight losses of the other tubers. Both kinds of losses were higher in cv. Liseta, in tubers with lower fresh weights and in tubers from the first harvest. Almost all minitubers ≥0.5 g from later harvests and from both cultivars survived storage for 1.5 years. Deterioration occurred mainly from 6 to 12 months of storage. Tubers which deteriorated during cold storage had already shown high weight losses during curing.     

The effect of controlled atmosphere storage at 4°C on crisp colour and on sprout growth,rotting and weight loss of potato tubers

Summary After three weeks curing at 10°C, potato tubers cv. Record were stored at 4°C under different controlled atmospheres (CA) for six months to study the effect on crisp fry colour, sprout growth and rotting. Combinations of low levels of CO₂ (0.7–1.8%) and low levels of O₂ (2.1–3.9%) gave a significantly lighter crisp colour, low sprout growth and fewer rotted tubers compared with 0.9% CO₂ and 21.0% O₂. Tubers stored in these conditions. showed a significantly higher weight loss and shrinkage after reconditioning. High CO₂: low O₂ combinations during storage completely inhibited sprout growth and caused the darkest crisp colour, but after reconditioning tubers gave the same level of sprouting and crisps as light as the other CA combinations. Furthermore these combinations, especially CO₂ at 10 or 15%, increased the onset of rotting. Also our results showed that at low concentrations of CO₂ (0.7–1.6%), and low O₂ (2–2.4%) there was an increase in tuber rotting.     

The effect of temperature and light during storage of young seed potatoes on initial plant development at early plantings

Summary Young seed tubers of several cultivars were exposed to storage temperatures of 4–24°C in light and dark intended to optimise their growth vigour following early plantings. In five experiments during four autumn and winter periods, the effects of storage conditions on subsequent initial plant development in the glasshouse were studied. Storage of seed potatoes for 2 months at temperatures of 12°C or higher greatly increased early plant development of five cultivars following early plantings. Light during storage had a favourable effect, but desprouting before planting was greatly disadvantageous.     

Effect of wet incubation time and temperature on infection, and of storage time and temperature on soft rot lesion expansion in potatoes inoculated withErwinia carotovora ssp.Carotovora

Summary Infection and lesion expansion studies were carrried out on potato tubers. In the infection study, the tubers were inoculated withErwinia carotovora ssp.carotovora (Ecc) and exposed to incubation temperatures of 10–25 °C for 3–48 h of wetness. In the lesion expansion study, the tubers were exposed to 12 h of wetness at 20 °C to establish infection, and then·stored at temperatures of 4–16 °C for 15–90 d, at 95% RH. The volume of diseased tissue was determined and the data were transformed to proportion of maximum volume diseased (PVD). Infection was close to zero for 3 and 6 h wet incubation time, regardless of incubation temperature, and reached the maximum in 12 h of wetness at 20 °C. Significant lesion expansion occurred at a storage temperature of 16 °C after about 60 d of storage time. Cubic models of infection and lesion expansion potentials explained 95 and 96% of the variations in infection and lesion expansion, respectively.     

Loss of vitamin C (L-ascorbic acid) during long-term cold storage of Dutch table potatoes

Summary Loss of vitamin C (L-ascorbic acid) from Dutch table potatoes during storage at 5–6°C over 8 months from November to July, was studied in two seasons. L-Ascorbic and dehydroascorbic acid were analysed by HPLC. The amount of dehydroascorbic acid was negligible. Total loss of L-ascorbic acid varied between 21 and 60%. Some potato lots lost L-ascorbic acid rapidly in the first four months, others more gradually over the whole storage period. The L-ascorbic acid levels detected were 75–150% higher in the period March–June, but 35% lower in the period December–February than those indicated by the step-wise decreases in the Dutch Food Composition Table.     

Slow-growth in vitro conservation of potato germplasm at normal propagation temperature

Summary In-vitro conservation of microplants at 24±1 °C was investigated in six potato genotypes belonging to different maturity groups. Growth was controlled by using different concentrations of sucrose (20, 40 and 60 g 1⁻¹) alone or in combination with either mannitol (20 and 40 g 1⁻¹) or sorbitol (20 and 40 g 1⁻¹) in Murashige and Skoog medium. Maximum microplant survival (55.5–77.8%) after 12 months of storage was on medium supplemented with 20 g 1⁻¹ sucrose plus 40 g 1⁻¹ sorbitol. Microplants so conserved were in good to very good condition, without phenotypic abnormalities and had enough nodes for sub-culturing. Microplant survival and microplant condition were closely associated with each other but not with root growth. The success of conservation was unaffected by maturity group of the genotypes. This conservation approach at 24±1 °C can be an effective alternative to low temperature (6–8 °C) storage, especially in tropical and sub-tropical conditions, where the ambient temperatures in summer can reach 45–50°C.     

Prevention of after-cooking darkening of irradiated potatoes

Summary Potatoes of the variety ‘Kufri Chandramukhi’ exposed to 10 krad of gamma rays for sprout inhibition, tended to develop after-cooking darkening, after storage at 15°C, for over three months. The darkening could be prevented or reduced (a) by pre-peeling of tubers prior to cooking: or (b) by reconditioning the potatoes by keeping them at 34–35°C for 4–6 days; or (c) by soaking and cooking the tubers in solutions of diaminoethane-tetra-acetic acid disodium salt (EDTA) or citric acid. Prepeeled tubers cooked in the presence of the peel tissues or added phenolics like caffeic and chlorogenic acids showed darkening. The results implicate that this could be due to the interaction of phenolics with Fe⁺⁺ present in the tissues. The storage of irradiated tubers at low temperature also showed enhanced disapperance of carotenoids.     

The effect of storage conditions on chemical content of raw potatoes and texture of cooked potatoes

Summary Texture of boiled potato tubers (cv. Beate) was studied over several months of storage at either 4 or 8 °C, in relation to dry matter content, non-starch polysaccharides (NSP), methyl groups, glucose, starch and amylose. The dry matter content decreased significantly during storage at 4 °C, but increased at 8 °C due to evaporation. The insoluble NSP contained rhamnose, galactose, arabinose, xylose, mannose, fucose and glucose; the first three sugars decreased significantly after the first 7 weeks of storage. Fracturability and percent compression before break increased during storage at 8 °C, particularly percent compression after 15 weeks. The change in fracturability could partly be explained (R²=43.4%) by the content of the NSP and the increase in percent compression by dry matter (R²=91.8%). Changes in texture during storage at 4 °C, however, were not striking, and could not be explained by changes in the potato components that were analysed.     

Effect of Low Storage Temperature on Some of the Flavour Precursors in Garlic (Allium Sativum)

Garlic (Allium sativum) cloves were stored at ambient temperature and 4 °C for periods up to six months to establish the effect of position of the individual clove within the bulb and of low storage temperature on the composition of several flavours precursors and other organic sulphur compounds, measured by gradient High Pressure Liquid Chromatography. Levels of alliin, γ glutamyl allyl cysteine sulphoxide and γ glutamyl isoallyl cysteine sulphoxide were statistically significantly higher in outer than in inner cloves. There was no statistically significant change in levels of alliin, the major flavour precursor, in cloves stored at 4 °C, remaining in the average range 17.5±3.8–39.1±7.5 mM. However, isoalliin increased significantly during storage at 4 °C, rising from an average 0.6±0.2 mM (outer cloves)—0.7±0.4 mM (inner cloves) to 7.1±1.7 mM (outer cloves)—4.1±0.7 mM (inner cloves). A decline in other sulphur-containing compounds, most likely to be the peptides γ-glutamyl allylcysteine sulphoxide and γ-glutamyl isoallylcysteine sulphoxide, occurred at the same time and possibly contributed to the increase in the flavour precursor compounds. The degree of chemical changes during storage will be of interest to the food and pharmaceutical industries.     

An investigation of the level of reducing sugars in diploid potatoes before and after cold storage

Summary The reducing sugar content and chip colour were studied in diploid potatoes bred for superior table and chipping quality. The reducing sugar content in the tubers of 119 diploid clones was estimated before and after cold storage (4–6°C) in the years 1987–1991, and reducing sugar and chip colour were determined in 1990 and 1991 for 36 clones. Thirty two clones had a significantly lower reducing sugar content after cold storage than cv. Mila. The year of evaluation, storage temperature and genotype significantly affected the reducing sugar content.     

Shortening dormancy of seed potatoes by storage temperature regimes

Summary Four experiments (three with four cultivars, one with twenty cultivars) investigated the effect of different storage temperature regimes on the duration of dormancy of seed potatoes harvested immature. Regimes included constant temperatures (18 and 28°C), hot pre-treatments (20 days at 28°C and subsequently 18°C) and cold pre-treatments (20 days at 2°C and subsequently 18°C). Compared with 18°C, storage at 28°C slightly prolonged dormancy of some cultivars with a genetically short dormancy and shortened dormancy by up to 45 days in cultivars with a long dormancy. Some tubers of one cultivar lost their ability to sprout after storage at 28°C for 90 days. A hot pre-treatment shortened dormancy by 2–3 weeks on average, for all cultivars examined. A cold pre-treatment shortened dormancy by 2 weeks on average in some cultivars with a short dormancy and in all cultivars with a long dormancy.     

The feasibility of cool storing potatoes in different parts of Britain,by ventilating with cold outside air at 0–3°C

Summary Analyses of meteorological data suggest that prolonged cool storage of potatoes, by ventilating with cold outside air at 0–3°C, is a feasible proposition in areas of Britain other than Edinburgh where this technique has been successfully operated, since 1964–65, for storage periods of up to 6 months.     

Shelf life study of some Nigerian fruit juices inoculated with ascospores ofNeosartorya spp.

Mango, orange and pineapple juices containing various concentrations of sucrose were dispensed in 100 ml volumes into 100 ml conical flasks with stoppers. Each juice in a flask was inoculated with ascospores of one local isolate of eitherNeosartorya fischeri, N. fischeri var.spinosa orN. quadricincta to a final concentration of 120–140 ascospores/ml of juice, and then pasteurized at 80°C for 30 min. A set of 36 inoculated flasks with 12 controls was stored at 4–5°C and two sets, one protected with 100 mg/l sodium benzoate, were stored at room temperature (25–28°C). A shelf life study was carried out on all the juices for 64 days. Only fruit juices stored at 4–5°C and those containing sodium benzoate stored at room temperature were protected from spoilage by these fungi for 64 days. Addition of sucrose at levels of 9% to mango juice, 30% to pineapple juice and 31.5% to orange juice significantly (p=0.05) protected ascospores from inactivation during cold storage.     

Increase in phosphorylase activity during cold-induced sugar accumulation in potato tubers

Summary The accumulation of reducing sugars, sucrose and hexose phosphates in cv. Bintje and genotype KW77-2916 during storage at 2, 4, or 8°C was studied in relation to several catalytic activities. Bintje tubers accumulated sugars during storage at 2 or 4°C, whereas KW77-2916 showed reduced cold-sweetening at 2°C. The increase in glucose 6-phosphate and sucrose occurred concurrently and preceded the increase in reducing sugar concentration. Phosphorylase activity showed a strong interaction with temperature, storage duration and sugar accumulation in both genotypes. Invertase activity increased in Bintje concomitantly with the increase in reducing sugars, but this effect was less obvious in KW77-2916. The activities of other glycolytic and Krebs cycle enzymes showed no obvious correlation with sugar accumulation. It is suggested that the increase in phosphorylase activity acts as a triggering event in the sweetening of potato tubers during cold storage.     

Effects of nitrogen,phosphorus and potassium fertilizer treatments on weight loss and changes in chemical composition of potato tubers stored at 4°C

Summary Pot and field experiments were carried out to test fertilizer treatments on the behaviour of potato tubers stores at 4°C and ≥90% relative humidity for 6 months. Weight losses (separated into water and dry matter) were enhanced after N and K fertilization and decreased by increasing P supply. Glucose and fructose contents were reduced at harvest by high N-fertilizer rates compared to no or low fertilization, but throughout storage reducing sugar accumulation was increased, sucrose reduction was decreased and ascorbic acid was increased. K fertilization affected the chemical composition of the tubers somewhat similar to that of nitrogen fertilization. High initial nitrate content of the tubers seemed to be increased and low nitrate values were decreased during storage. The tubers from pot experiments showed similar changes but of greater magnitude.     

The relationship between temperature and sprout growth in stored seed potatoes

Summary Sprout growth in a range of European cultivars was studied over two seasons at constant temperatures from 2 to 25°C, with an additional 33 (day)/22°C (night) treatment in the second season. There were only minor differences in the response of the cultivars and the optimum for sprout growth was at 15–18°C in all cases, when measured over an extended period, but initially sprout growth was more rapid at 23–25°C. Sprout growth at 23–25°C was frequently arrested by sub-apical necrosis, and at these temperatures the sprouts remained short enough for the tubers to be planted by hand without desprouting.     

Possible involvement of fructose 1,6-bisphosphatase in cold-induced sweetening of potato tubers

Summary In measuring fructose 1,6-bisphosphatase (EC 3.1.3.11; FBPase) in potato tubers, we used anti PFP antibodies to ensure that the assay was specific for FBPase and that PPi:fructose 6-phosphate 1-phosphotransferase (EC 2.7.1.90: PFP) did not contribute to the production of fructose 6-phosphate (Fru-6-P). The involvement of cytosolic FBPase in cold sweetening was determined by monitoring enzyme activity during storage ofSolanum tuberosum cv. Erntestolz tubers at 2 or 8°C. In contrast to the rapid increase in sucrose and reducing sugars, the specific activity of FBPase showed no change and PFP rose slightly during storage at 2°C. Sugar concentrations and enzyme activities remained virtually unchanged during storage at 8°C. These data allow the interconversion of fructose 1.6-bisphosphate (Fru-1,6-P₂) to Fru-6-P and vice versa by FBPase and PFP, respectively, in potato tubers, but do not support a causal relationship between coarse metabolic control of FBPase and cold-induced sweetening.