The fate of pyruvate, a key product of glycolysis, is influenced by the cellular conditions and the type of organism involved. Under anaerobic conditions in human cells, pyruvate is converted into lactate, while in yeast or under hypoxic conditions, it is transformed into ethanol and carbon dioxide, a process fundamental to alcohol fermentation and the production of beverages like beer. This fermentation process has historical significance, as it may have played a role in the development of human societies.
In aerobic conditions, pyruvate is further processed into Acetyl CoA, which is essential for aerobic cellular respiration. However, when oxygen is scarce, fermentation becomes crucial for regenerating NAD+ from NADH, allowing glycolysis to continue. Glycolysis itself converts one molecule of glucose (a 6-carbon sugar) into two molecules of pyruvate (3-carbon compounds), yielding a net gain of 2 ATP and 2 NADH.
During alcohol fermentation, pyruvate undergoes decarboxylation, where a carbon atom is removed in the form of carbon dioxide, resulting in acetaldehyde. This intermediate is then reduced by NADH to produce ethanol, effectively recycling NAD+ to sustain glycolysis. The reaction can be summarized as follows:
1. Pyruvate (C3H4O3) → Acetaldehyde (C2H4O) + CO2
2. Acetaldehyde + NADH → Ethanol (C2H6O) + NAD+
In contrast, lactic acid fermentation, also known as the Cori cycle, involves the direct reduction of pyruvate by NADH to form lactate and regenerate NAD+. This process is vital for cells like red blood cells, which rely solely on glycolysis and fermentation for energy. The reaction can be summarized as:
Pyruvate (C3H4O3) + NADH → Lactate (C3H6O3) + NAD+
Both fermentation pathways serve the essential function of maintaining glycolysis in the absence of oxygen, ensuring that cells can continue to produce energy even under challenging conditions.