This paper discusses the use of cassava in foods and animal feed. Industrial processing of cassava and waste management in cassava starch factories are also considered.

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The root tuber crops, including cassava, sweet potato, yams, and aroids, enjoy considerable importance as a vegetable, staple food, or raw material for small-scale industries at a global level, particularly in the less developed tropical countries. The perishability and postharvest loses of root and tuber crops are the major constraints in the utilization of these crops. Several simple, low-cost traditional methods are being followed by farmers in different parts of the world to store different root and tuber crops in the fresh state. An account of different storage practices and constraints is reviewed in this article. Some of these methods have been studied and evaluated by different research workers. Several modern techniques, including refrigerated cold storage, freezing, chemical treatments, wax coating, and irradiation, for storing fresh tropical tubers are also reviewed. The pre- and postharvest factors to be considered for postharvest storage of different root and tuber crops are incorporated into the review.

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The properties of Cephalosporium eichhorniae 152 (ATCC 38255) affecting protein production from cassava carbohydrate, for use as an animal feed, were studied. This strain is a true thermophile, showing optimum growth at 450 to 47°C, maximum protein yield at 45°C, and no growth at 25°C. It has an optimum pH of about 3.8 and is obligately acidophilic, being unable to sustain growth at pH 6.0 and above in a liquid medium, or pH 7.0 and above on solid media. The optimum growth conditions of pH 3.8 and 45°C were strongly inhibitive to potential contaminants. It rapidly hydrolyzed cassava starch. It did not utilize sucrose, but some (around 16%) of the small sucrose component of cassava was chemically hydrolyzed during the process. Growth with cassava meal (50 g/liter [circa 45 g/ liter, glucose equivalent]) was complete in around 20 h, yielding around 22.5 g/liter (dry biomass), containing 41% crude protein (48 to 50% crude protein in the mycelium) and 31% true protein (7.0 g/liter). Resting and germinating spores (106 to 108 per animal) injected by various routes into normal and y-irradiated 6-weekold mice and 7-day-old chickens failed to initiate infections.