Mucor racemosus fermented glucose to ethanol, carbon dioxide, and glycerol. When this fungus was grown anaerobically in either the yeast or mycelial form, the catabolism ofglucose was very similar. Yeast cells shifted to aerobic conditions maintained a high flux of glucose carbon through the glycolytic and pentose phosphate pathways. Mycelial cells grown aerobically catabolized glucose in a manner consistent with a respiratory metabolism. Although there was no consistent pattern of glucose metabolism in the mycelial form of Mucor, growth in the yeast form consistently was correlated with a high flux of glucose carbon through the catabolic pathways.Mucor racenosus is a dimorphic phycomycete that can grow either as budding yeasts or as filamentous mycelia. Although the morphology of this fungus appears to be influenced by a variety of environmental factors (4, 14), the presence of a fermentable hexose is essential for the development of the yeast form (2). Larsen and Sypherd (8) showed, for example, that, although dibutyryl cyclic AMP (dbcAMP) induced yeast development in air, the presence of glucose was necessary to maintain the yeast form. Depending on the concentration of glucose in the growth medium, the morphology of M. rouxii, grown under anaerobic conditions (100% N2), varied from the mycelial form to the yeast form (2). Mooney and Sypherd (10) reported, however, that effects of glucose concentration on morphology were not observed with M. racemosus if one carefully regulated the flow rate of nitrogen through the culture. When M. genevensis yeast cells were grown in continuous culture with excess glucose, mycelial cells were not formed even at high oxygen concentrations (13). Indeed, these aerobic yeast cells continued to produce ethanol and carbon dioxide at a rate indicative of a fermentative metabolism. These workers (13) concluded that respiratory capacity was not correlated with morphology. In addition, Paznokas and Sypherd (12) measured the respiratory capacity of aerobic mycelia and aerobic dbcAMP-treated yeast and concluded that morphology was independent of respiratory capacity. The present study was designed to determine the nature of the relationship between the patterns of glucose carbon metabolism and the morphology of Mucor. Changes in the distribution or flux of carbon into the glucose catabolic pathways could reveal changes in metabolic intermediates, enzymes, or end products important to the regulation of morphogenesis.
MATEIUALS AND METHODSOrganism and culture conditions. Mucor racemosus (M. huitanicus) ATCC 1216B was used in all experiments. Sporangiospores were prepared as described by Paznokas and Sypherd (12). Cells were grown in either a complex medium consisting of 0.3% (wt/vol) yeast extract (Difco), 1% (wt/vol) peptone (Difco), and 2% (wt/vol) D-glucose; or a minimal medium consisting of 0.05% (wt/vol) yeast nitrogen base (Difco), 2% (wt/vol) D-glucose, 10 mM L-glutamate, 10 mM L-alanine, 10 mM L-aspartate, and 10 mM NH4Cl (J. Peters and P. S. Sypherd, J. Gen. Microbiol., in press)....