Transcript Document

NS 315
Unit 4: Carbohydrate
Metabolism
Jeanette Andrade MS,RD,LDN,CDE
Kaplan University
Objectives
We want to learn about:
 Glycolysis and ATP formation
 Understand Gluconeogenesis, when, where
and how
 Krebs Cycle and Electron Transport Chain
Definitions
 Glycolysis: central pathway for the catabolism of
carbohydrates; occurs in most organs
 Gluconeogenesis: Biosynthesis of new glucose; occurs
mainly in liver and sometimes in kidneys
 Glycogenesis: group of enzymatic reactions leading to
the formation of glycogen
 Glycogenolysis: group of enzymatic reactions that use
stored glycogen to form glucose
Definitions
 Krebs cycle- series of enzymatic reactions in aerobic
organisms involving oxidative metabolism of acetyl units
and producing high-energy phosphate compounds, which
serve as the main source of cellular energy
 Electron Transport Chain (ETC)- Composed of
mitochondrial enzymes that transfers electrons from one
transport to another, resulting in the driving force for the
formation of ATP
 Oxidative phosphorylation- Process occurring in the
cell, which produce energy and synthesizes ATP
Definitions
 Pyruvate: final 3-carbon molecule of glycolysis, involved in the
Krebs cycle which facilitates energy production
 Adenosine diphosphate/Adenosine triphosphate: energy
storing molecule used by an organism on a daily basis
 NAD/NADPH: Reducing agent in several anabolic reactions such
as lipid and nucleic acid
 FAD/FADH: Reducing agent in several anabolic reactions such
as lipid
 Aerobic: in the presence of oxygen
 Anaerobic: no presence of oxygen
Glycolysis Animation
 Please review the website for an animated
description of glycolysis pathway and we will
discuss it in 5 minutes
http://highered.mcgraw-hill.com/sites/0072507470/student_view0/chapter25/animation__how_glycolysis_works.html
Fates of Pyruvate
Under aerobic conditions
In most aerobic organisms,
pyruvate continues in the
formation of Acetyl CoA and
NADH that follows into the
Krebs cycle and ETC
Under anaerobic conditions
Under anaerobic conditions, such
as during exercise or in red blood
cells (no mitochondria), pyruvate is
reduced to lactate by lactate
dehydrogenase producing NAD.
Lactate can be converted back to
glucose in the Cori Cycle.
Pathways From Glycolysis
Aerobic- with oxygen
Anaerobic- without oxygen
 The main energy-releasing
 Fermentation pathway and
pathway in most human
cells
 Continues in the
mitochondrion where
oxygen serves as the final
electron receptor
 1 glucose + 6 oxygen  6
carbon dioxide +6 water
 36 or 38 ATPs are
produced (total after all
cycles: glycolysis, krebs
and ETC)
anaerobic electron transportmany bacteria and humans,
when oxygen is limited, use
this pathway
 Ends in the cytoplasm where
other substances besides
oxygen are the final electron
receptor
 Only 2 ATP are produced
 Lactate may be end product
until oxygen becomes
available
Gluconeogenesis
 During starvation (not eating for 16 hours
plus), the brain can use ketone bodies for
energy by converting to Acetyl CoA; usually
gluconeogenesis creates glucose when
glycogen stores are depleted
 Synthesis of glucose from 3-4 carbon
precursors is a reversal of glycolysis
2 pyruvate + 2 NADH + 4 ATP + 2 GTP
glucose + 2 NAD+ + 4 ADP + 2 GDP + 6 Pi
Gluconeogenesis
 3 reactions in glycolysis are essentially
irreversible, thus they are bypassed in
gluconeogenesis:



Hexokinase (1)
Phosphofructokinase (3)
Pyruvate Kinase (10)
 Shares 7 of the 10 steps in glycolysis
Glycolysis vs Gluconeogenesis
Fed state
Fasting state
Cytoplasm
Cytoplasm
All cells
Liver mostly,
but also kidney
These three irreversible
steps are important in
the regulation and
control of glycolysis and
gluconeogenesis!
Krebs Cycle
 Also known as the citric acid cycle or tricarboxylic acid
(TCA) cycle
 Under aerobic conditions pyruvate enters the mitochondrial
MATRIX and is oxidized to Acetyl CoA, which then enters the
Krebs cycle
 Krebs cycle can occur after glycolysis, after Beta-oxidation or
protein degradation to provide energy for cellular respiration
 Equation for Krebs cycle with the beginning products and the
ending. 8 steps involved
2 pyruvate + 2 GDP + 2 H3PO4 + 4 H2O + 2 FAD + 8 NAD+ ----> 6 CO2 + 2 GTP + 2 FADH2 + 8 NADH
http://vincentimbe.files.wordpress.com/2007/11/krebs-cycle.jpg
Fig. 3-19, p. 87
Krebs Cycle
 Please go to: http://highered.mcgraw-
hill.com/sites/0072507470/student_view0/cha
pter25/animation__how_the_krebs_cycle_wo
rks__quiz_1_.html and we will discuss the
krebs cycle after the animated movie.
Activation of Pyruvate
 First step activates pyruvate to acetyl CoA.
 Pyruvate Dehydrogenase Complex (PDHC)
catalyzes the oxidative decarboxylation of pyruvate to
acetyl CoA
 PDHC is a multienzyme comprising of 5 coenzymes
(some vitamins): thiamin pyrphosphate (thiamin), CoA,
lipoic acid, FAD (riboflavine) and NAD (niacin)
PDHC
http://chemistry.uah.edu/Faculty/ciszak/acetyl_drawing.jpg
Summary TCA
 Occurs in the mitochondrial matrix
 Uses acetyl CoA to produce:

3 NADH, 1 FADH, 1 GTP, 2CO2
 Produce intermediates for biosynthetic pathways
such as amino acid synthesis, gluconeogenesis,
pyrimidine synthesis, phorphyrin synthesis, fatty
acid synthesis, isoprenoid synthesis.
Electron Transport Chain (ETC)
 Final pathway by which electrons generated from
oxidation of carbs, protein, and fatty acids are ultimately
transferred to O2 to produce H2O
 Located in the inner mitochondrial membrane
 Electrons travel down the chain, pumping protons into the
intermembrane space creating the driving force (“proton
gradient”) to produce ATP in a process called oxidative
phosphorylation
 There are 4 complexes that comprise the ETC
Electron Transport Chain
 Please go to:
http://vcell.ndsu.edu/animations/etc/movie.ht
m and we will discuss the ETC after the
animation
Summary ETC
 Reduced electron carriers NADH & FADH2 reduce O2 to H2O via
the ETC. The energy released creates a proton gradient across
the inner mitochondrial membrane. The protons flow down this
concentration gradient back across the inner mitochondrial
membrane through the ATP Synthase Enzyme. This driving force
makes this enzyme rotate, and this conformational change
generates enough energy to make ATP.
 Oxidation of NADH to NAD+ pumps 3 protons which charges the
electrochemical gradient with enough potential to generate 3 ATPs.
 Oxidation of FADH2 to FAD+ pumps 2 protons which charges the
electrochemical gradient with enough potential to generate 2 ATPs.