Biochemistry Lecture 1. Blooms Taxonomy Richard C. Overbaugh, Lynn Schultz Old Dominion University.

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Biochemistry Lecture 1

Transcript of Biochemistry Lecture 1. Blooms Taxonomy Richard C. Overbaugh, Lynn Schultz Old Dominion University.

Page 1: Biochemistry Lecture 1. Blooms Taxonomy Richard C. Overbaugh, Lynn Schultz Old Dominion University.

Biochemistry

Lecture 1

Page 2: Biochemistry Lecture 1. Blooms Taxonomy Richard C. Overbaugh, Lynn Schultz Old Dominion University.

Bloom’s Taxonomy

Richard C. Overbaugh, Lynn SchultzOld Dominion University

Page 3: Biochemistry Lecture 1. Blooms Taxonomy Richard C. Overbaugh, Lynn Schultz Old Dominion University.

Student Objectives for this course

• Calculate bioenergetic parameters and evaluate carbon molecules reactions

• Reproduce and explain key metabolic processes: glycolysis, TCA cycle, electron transport and oxidative phosphorylation, fatty acid oxidation

• Analyze protein structure and function and evaluate different methods used to assess and test structure and function

• Trace key metabolites through key pathways, design experiments to test carbon flux

• Compare and contrast modes of metabolism regulation and judge the effects of different modes

Page 4: Biochemistry Lecture 1. Blooms Taxonomy Richard C. Overbaugh, Lynn Schultz Old Dominion University.

Biochemistry is the chemistry of

Living Systems• The Chemistry of Carbon and Water• Themes for this course:

– The transformation of energy– Levels of complexity

Page 5: Biochemistry Lecture 1. Blooms Taxonomy Richard C. Overbaugh, Lynn Schultz Old Dominion University.

Cells

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Cells

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Levels of Complexity

Lipids

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The Inner Life of the Cell

• http://multimedia.mcb.harvard.edu/anim_innerlife.html

Page 9: Biochemistry Lecture 1. Blooms Taxonomy Richard C. Overbaugh, Lynn Schultz Old Dominion University.

Why CarbonBond Strength

(kJ/mol)

C – C 347 – 356

C = C 611

C = C 837

C – O 336

C – H 356 – 460

Si – Si 230

Si – O 368

O – O 146

O = O 498

N – N 163

N = N 418

N = N 946

What can we learn from this?

• C – C bond is stronger than C – O– Stable in oxygen rich

environment!

• Two C – C bonds are stronger than one C = C– Chains are stable!

• C – H bond is strong– Hydrocarbons stable at

room temperature!

Page 10: Biochemistry Lecture 1. Blooms Taxonomy Richard C. Overbaugh, Lynn Schultz Old Dominion University.

Important Functional Groups

• Alcohol• Thiol• Amine• Ether• Thioether• Peroxide• Disulfide• Aldehyde• Ketone

• Carboxylic acid• Ester• Anhydride• Amide• Thioester• Phosphate• Phosphoester• Phosphoanhydride

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Carbon and Functional Groups

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Other biomolecules

NADP+

PEP

Phosphatidylcholine

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Bioenergetics

CellReactants Products

Steady State = constant flux

STHG

QRTGG ln'0

Structural differences between reactants and products

Concentration differences between reactants and products

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Water

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Hydrogen Bonds

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Water

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Colligative Properties

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pH

pH = -log[H+]

214- M101]OH][H[ wK

14]OHlog[]Hlog[ -

14pOHpH

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Acids

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Buffers

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HA][

]A][H[ -

aKHA H+ + A-

HA][

]A[logppH

-

aK

Hendeson Hasselbalch Equation

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Summary

• Biochemistry is the chemistry of living things– Which is the chemistry of carbon and

water

• Carbons unique bonding properties• Water: hydrogen bonds and

ionization• Buffers and pH