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Glycolysis
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is the sequence
of reactions that metabolizes one molecule of glucose to two molecules
of pyruvate with the concomitant net production of two molecules of
ATP. This process is anaerobic (i.e., it does not require O2) because it
evolved before substantial amounts of oxygen accumulated in the
atmosphere.
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Pyruvate can be further processed
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anaerobically to lactatelactic acid fermentation) or ethanol (alcoholic fermentation).
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Starch and glycogen are digested primarily by
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the pancreatic enzyme
a-amylase and to a lesser extent by salivary α-amylase.
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Amylase cleaves
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the
α-1,4 bonds of starch and glycogen, but not the α-1,6 bonds
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maltase cleaves
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maltose into two glucose molecules, whereas α-glucosidase
digests maltotriose and any other oligosaccharides that may have escaped
digestion by the amylase
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Glucose
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common and important fuel. In mammals, glucose is the
only fuel that the brain uses under nonstarvation conditions and the only fuel
that red blood cells can use at all.
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Why is glucose instead of some other
monosaccharide such a prominent fuel?
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First, glucose is one of several monosaccharides formed from form-aldehyde
under prebiotic conditions, and so it may have been available as a fuel source
for primitive biochemical systems. Second, glucose has a low tendency,
relative to other monosaccharides, to nonenzymatically glycosylate proteins.
In their open-chain forms, monosaccharides contain carbonyl groups that can
react with the amino groups of proteins to form Schiff bases, which rearrange
to form a more stable amino–ketone linkage.
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What happens in Stage one of glycolysis
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Stage 1 is the trapping and preparation phase. No ATP
is generated in this stage. Stage 1 begins with the conversion of
glucose into fructose 1,6-bisphosphate, which consists of three steps:
a phosphorylation, an isomerization, and a second phosphorylation
reaction. The strategy of these initial steps in glycolysis is to trap the
glucose in the cell and form a compound that can be readily cleaved
into phosphorylated three-carbon units. Stage 1 is completed with the
cleavage of the fructose 1,6-bisphosphate into two three-carbon
fragments. These resulting three-carbon units are readily
interconvertible. In stage 2,
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In stage 2, of glycolysis
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ATP is harvested when the three-carbon
fragments are oxidized to pyruvate.
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Glucose enters cells through specific transport proteins (p. 477) and has one
principal fate: it is phosphorylated by ATP to form glucose 6-phosphate why does this matter?
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1) glucose 6-phosphate cannot pass through
the membrane because it is not a substrate for the glucose transporters, and
(2) the addition of the phosphoryl group acts to destabilize glucose, thus
facilitating its further metabolism. The transfer of the phosphoryl group from
ATP to the hydroxyl group on carbon 6 of glucose is catalyzed by hexokinase.
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Kinases
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are
enzymes that catalyze the transfer of a phosphoryl group from ATP to an
acceptor.
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The Cori cycle is
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Lactate formed by active muscle is converted into glucose by the liver. The cycle shifts part of the metabolic burden of active muscle to liver. Thus, the liver restores the level of glucose necessary for active muscle cells, which derive ATP from the glycolytic conversion of glucose into lactate.
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Lactose intolerance, or hypolactasia,
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"Deficiency" is not quite the appropriate term because a decrease in lactase is normal in the course of development in all mammals.
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What happens to the lactose in the intestine of a lactase-deficient person?
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Lactose is a good energy source for microorganisms in the colon, and they ferment it to lactic acid while generating methane (CH4) and hydrogen gas (H2).
The gas produced creates an uncomfortable feeling of gut distension and the annoying problem of flatulence.
The lactate produced by the microorganisms is osmotically active and draws water into the intestine, as does any undigested lactose, resulting in diarrhea.
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Hexokinase
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catalyzes the transfer of a phosphoryl group
from ATP to a variety of six-carbon sugars (hexoses), such as glucose and
mannose. Hexokinase, like adenylate kinase (Section 9.4) and all other
kinases, requires Mg2+ (or another divalent metal ion such as Mn2+) for
activity. The divalent metal ion forms a complex with ATP.
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