The yeasts Candida utilis and Saccharomycopsis fibuliger were propagated as a source of single-cell protein in a continuous, mixed, aerobic, single-stage cultivation on blancher water generated during potato processing. A series of steadystate experiments based on a two-level factorial design, half-replicate modified with an intermediate experiment, was performed to determine the effect of pH, 3.8 to 4.8; dissolved oxygen, 42 to 80% saturation; dilution rate, 0.17 to 0.31 h-1I and temperature, 27 to 320C on the amount of carbon consumed, the rate of carbon consumption (Rc), the amount of reducing sugar consumed, the rate of sugar consumption (Rg), the amount of protein produced, the rate of protein production (Rp), the yield from carbon, and the yield from reducing sugar. The results were analyzed by stepwise multiple regression and Fisher's least significant difference test. Analyses showed that high dilution rates resulted in increased Rc, Rg, and Rp and indicated that a rate of 0.31 h-1 was below the critical dilution rate. A temperature of 320C increased the amount of carbon consumed by 34%. A pH of 4.3 to 4.8 increased the amount of protein produced. The yield from carbon was constant, and the relatively high yield from reducing sugar indicated that other substrates were consumed. Dissolved oxygen was in excess at 42% saturation and above. Since C. utilis predominated the mixed cultures and amylase production appeared to be limited, a single-stage fermentation lacked efficiency. The experimental design allowed preliminary optimization of major environmental variables with relatively few experiments and provided a basis for future kinetic studies.
The kinetics of growth and amylase production of Saccharomycopsis fibuligera were studied in a chemostat on a synthetic potato processing blancher water. Dilution rates (D) from 0.101 to 0.480 h-' were examined. A mathematical model based on the Monod equation was developed. The yield of cell mass from carbohydrates was constant and equal to 0.84. The maximum specific growth rate and the Monod constant were determined to be 0.596 h-1 and 0.226 mg/ml, respectively. An equation for the steady-state starch concentrations was empirically derived. The steady-state noncarbohydrate carbon levels rose linearly with D. Reducing sugars were the growth-limiting substrate, and their steady-state levels conformed to Monod kinetics. The yield of amylase from the cell mass (Ye) declined as D rose and was described by the equation Y, = (-8.005D + 4.076). The model predicted that the maximum production of cell mass should occur at D = 0.35 h-' and the maximum production of amylase should occur at D = 0.22 h-'. The mathematical model presented agreed with the experimental results in its prediction of the steady-state level of reducing sugar, starch, cell mass, and amylase concentrations as well as the productivity of amylase.
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