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ALCOHOL DEHYDROGENASE A comprehensive overview and experimental analysis Elliott Weideman.

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ALCOHOL DEHYDROGENASE A comprehensive overview and experimental analysis Elliott Weideman
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Page 1: ALCOHOL DEHYDROGENASE A comprehensive overview and experimental analysis Elliott Weideman.

ALCOHOL DEHYDROGENASE

A comprehensive overview and experimental analysis

Elliott Weideman

Page 2: ALCOHOL DEHYDROGENASE A comprehensive overview and experimental analysis Elliott Weideman.

ALCOHOL DEHYDROGENASE

What is it? ADH Enzyme that breaks down alcohols

Why is it important? In most animals it is used to metabolize

alcohols that have been ingested. Yeasts and bacteria use ADH in reverse to

convert sugars into ethanol via fermentation.

Page 3: ALCOHOL DEHYDROGENASE A comprehensive overview and experimental analysis Elliott Weideman.

ALCOHOL DEHYDROGENASE

RCH2OH + NAD+

RCHO + NADH + H+

Chemical Reaction

ADH

NAD+ is needed as an important cofactor for ADH

Page 4: ALCOHOL DEHYDROGENASE A comprehensive overview and experimental analysis Elliott Weideman.

Experimental Question What is the rate of reaction that ADH is capable

of maintaining?

Experimental Design Overview Chemical assay techniques using

spectrophotometry to measure the amount of product synthesized from ADH.

ALCOHOL DEHYDROGENASE

Page 5: ALCOHOL DEHYDROGENASE A comprehensive overview and experimental analysis Elliott Weideman.

Materials Yeast ADH - Provided from Sigma

NAD+ - Provided from Sigma

95% Ethanol - Provided from Sigma

Tris Buffer pH 8 - Provided from Acros

Equipment Genesys 10 UV/vis Spectrophotometer - Provided

from ThermoSpectronic

Cuvettes - Provided from Fisher Scientific

ALCOHOL DEHYDROGENASE

S. Cerevisiae

Page 6: ALCOHOL DEHYDROGENASE A comprehensive overview and experimental analysis Elliott Weideman.

Procedure Obtain Tris buffer - pH 8 Prepare ADH enzyme by adding dry reagent with

water to equal 20 units/mL Dilute Ethanol to concentrations of

0.7M, 0.375M, 0.1M, 0.5M and 0.25M C1 V1 =C2 V2

Prepare NAD+ to final concentration of

15mM

ALCOHOL DEHYDROGENASE

Page 7: ALCOHOL DEHYDROGENASE A comprehensive overview and experimental analysis Elliott Weideman.

Procedure Enzyme assays by combining the following

900uL Tris buffer 33uL NAD+ 33uL ethanol (0.7M, 0.375M, 0.1M, 0.05M, and 0.025M) 33uL ADH

The solution was mixed thoroughly and gently before quickly being measured in the spectrophotometer at 340nm

ALCOHOL DEHYDROGENASE

Page 8: ALCOHOL DEHYDROGENASE A comprehensive overview and experimental analysis Elliott Weideman.

Procedure Assays were measured for absorbance at T0 and

T1

Average rate (Abs340 T1 – Abs340T0/min) was recorded

Three trials were run for each [ethanol]

ALCOHOL DEHYDROGENASE

Page 9: ALCOHOL DEHYDROGENASE A comprehensive overview and experimental analysis Elliott Weideman.

Data

ALCOHOL DEHYDROGENASE

[Ethanol] M Abs T0 Abs T1

Rate (ΔA340

/min)

Average Rate

0.73+ 3+ -

0.082+2.923 3+ 0.080+2.917 3+ 0.083+

0.3752.466 3+ 0.534+

0.539+1.072 1.102 0.0301.946 3+ 1.054+

0.11.066 2.182 1.116

1.0031.215 2.229 1.0141.283 2.163 0.880

0.050.904 1.443 0.539

0.5520.854 1.47 0.6160.697 1.197 0.500

0.0250.651 1.152 0.501

0.4350.566 0.928 0.3620.636 1.077 0.441

Page 10: ALCOHOL DEHYDROGENASE A comprehensive overview and experimental analysis Elliott Weideman.

Results Lineweaver-Burke Data and Plot

ALCOHOL DEHYDROGENASE

1/[Ethanol] 1/Abs T1

1.4285 0.539539

2.6667 0.617408

10 0.84685

20 1.13729

40 1.62507

0 5 10 15 20 25 30 35 40 450

0.2

0.4

0.6

0.8

1

1.2

1.4

1.6

1.8

f(x) = 0.0276960846636675 x + 0.542802013525725R² = 0.993762636749275

1/[Ethanol] M

1/A

bsorb

an

ce

34

0n

m

Page 11: ALCOHOL DEHYDROGENASE A comprehensive overview and experimental analysis Elliott Weideman.

Results Vmax – The fastest the enzyme can perform

under ideal circumstances 0.0511 M/min

Km – Michaelis constant (several rate constants) 1.8423 mM

ALCOHOL DEHYDROGENASE

3D rendering of ADH

Page 12: ALCOHOL DEHYDROGENASE A comprehensive overview and experimental analysis Elliott Weideman.

Discussion Drawbacks

Incorrect preparation of trial 2 assay for 0.375M Ethanol Possible contamination when preparing NAD+

Inconsistent handling of cuvettes when loading into spectrophotometer Uniform mixing Time loading

Use less ADH enzyme to get a more accurate reading of the rate of reaction

Positive control – Lacking an inhibited version of the enzyme

ALCOHOL DEHYDROGENASE

Page 13: ALCOHOL DEHYDROGENASE A comprehensive overview and experimental analysis Elliott Weideman.

Discussion Future Research

Investigate performance of ADH with other concentrations of ethanol under different temperatures or levels of pH

Run the reaction backwards by manipulating the equilibrium level

Use other versions of ADH and or types of alcohols Applications to medical industry involving alcoholism

and genetics

ALCOHOL DEHYDROGENASE

Page 14: ALCOHOL DEHYDROGENASE A comprehensive overview and experimental analysis Elliott Weideman.

Discussion Application

Cirrhosis of liver – condition marked by chronic liver disease and subsequent degeneration

ALCOHOL DEHYDROGENASE

Page 15: ALCOHOL DEHYDROGENASE A comprehensive overview and experimental analysis Elliott Weideman.

ReferencesBendinskas, K., DiJiacomo, C., Krill, A., & Vitz, E. 2005. Kinetics of

alcohol dehydrogenase – catalyzed oxidation of ethanol followed by visible spectroscopy, Journal of Chemical Education, 82(7), 1068-1070.

Edenberg, H. J. 2007. The genetics of alcohol metabolism: Role of alcohol dehydrogenase and aldehyde dehydrogenase variants. Alcohol Research & Health, 30(1), 5-13.

Voss, C. Gruber, K. Faber, T. Knaus, P. Macheroux, W. Kroutil. 2008. J. Am. Chem. Soc, 130, 13969-13972.

Laboratory Manual, 2012.

Dr. Christenson

ALCOHOL DEHYDROGENASE


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