Catalase AEBI

[13]
CATALASEm Vitro
121
High concentrations of polyvalent anions, which may be contained in

test samples or in the batch of glutathione reductase used, can inhibit
glutathione peroxidase.
As differences in enzymic properties, e.g., in kinetics, of glutathione
peroxidase can not be excluded in different tissues or species, optimal
substrate concentrations, if in doubt, should be reassessed.
If the activity measured in crude samples is to be assigned to glutathfone peroxidase unequivocally, a separation step and characterization, e.g., by correlating selenium content and enzymic activity during
fractionation, should be considered.
[13] Catalase in V i t r o
By HUGO AEB1
2H202 eatal,s~2H20 + 02
ROOH + AH2 catalascH20 + ROH + A
(1)
(2)
Catalase exerts a dual function: (1) decomposition of H202 to give H20

and 02 [catalytic activity, Eq. (1)] and (2) oxidation of H donors, e.g.,
methanol, ethanol, formic acid, phenols, with the consumption of I mol of
peroxide [peroxidic activity, Eq. (2)].
Kinetic Properties
The predominating reaction depends on the concentration of H donor
and the steady-state concentration or rate of production of H202 in the
system. In both cases the active catalase-H202 complex I is formed first.
The decomposition of H202, in which a second molecule of H202 serves
as H donor for complex I, proceeds exceedingly rapidly (rate constant k
107 liters mol -t sec -t) whereas peroxidative reactions proceed relatively
slowly (k - 102-103). t
The kinetics of catalase do not obey the normal pattern. On the one
hand it is not possible to saturate the enzyme with "substrate" within the
feasible concentration range (up to 5 M H202), and on the other there is a
rapid inactivation of catalase at H202 concentrations above 0.1 M, when
the active enzyme-H202 complex I is converted to the inactive complexes II or III. Measurements of enzyme activity at substrate saturation
1 B. Chance, Acta Chem. Scand. 1, 236 (1947).
METHODS IN ENZYMOLOGY, VOL. 105
Copyright 1984 by Academic Press. Inc.

All rights of reproduelion in any form reserved,
ISBN 0.12-182005-X
122
FORMATION OR REMOVAL OF OXYGEN RADICALS
[13]
or determination of the Ks is therefore impossible. In contrast to reactions

proceeding at substrate saturation, the enzymic decomposition of H202 is
a first-order reaction, the rate of which is always proportional to the
peroxide concentration present. Consequently, to avoid a rapid decrease
in the initial rate of the reaction, the assay must be carried out with
relatively low concentrations of H202 (about 0.01 M). 2 As the activation
energy for the decomposition of H202 catalyzed by catalase is very low
(2500-7100 kJ/mol), there is only slight dependence on temperature
(Qi0 = 1.05-1.12). The decomposition of H202 initially (approx. 0-30 sec)
follows that of a first-order reaction with H202 concentration between
0.01 and 0.05 M. The rate constant (k) for the overall reaction is given by
k = (1/At)(ln SI/S2) = (2 3/At)(log SI/S2)
(3)
where At = t2 - t~ = measured time interval and S~ and $2 = H202

concentrations at times tl and t2. The constant k can be used as a direct
measure of the catalase concentration. In studies with purified enzyme
preparations the specific activity (k'0 is obtained by dividing k by the
molar concentration of catalase (e).
kl = k/e
(liters mol -l sec -l)
(4)
The value for k'~ for pure catalase from human erythrocytes is 3.4 x 10 7
(liters mol-~ sec-~). This value is used to calculate the absolute content o f
enzyme in blood and tissues. 3
Assay Method
Principle
In the ultraviolet range H202 shows a continual increase in absorption
with decreasing wavelength. The decomposition of H202 can be followed
directly by the decrease in absorbance at 240 nm (e240 = 0.00394 --- 0.0002
liters mmol -I mm-I). 4 The difference in absorbance (AA240) per unit time
is a measure of the catalase activity.
To avoid inactivation of the enzyme during the assay (usually 30 sec)
or formation of bubbles in the cuvette due to the liberation of 02, it is
necessary to use a relatively low H202 concentration (10 mM). The H~O2
concentration is critical inasmuch as there is direct proportionality between the substrate concentration and the rate of decomposition. Due to
the special situation in catalase the dependence of the H202 decomposiR. K. Bonnichsen, B. Chance, and H. Theorell, Acta Chem. Scand. 1, 685 (1947).
R. K. Bonnichsen, this series, Vol. II, p. 781.
D. P. Nelson and L. A. Kiesow, A n a l Biochem. 49, 474 (1972).
[13]
CATALASEin Vitro
123
tion on the temperature is small (Qi0 - 1.1) so that measurements can be

carried out between 0 and 37; however, 20 is recommended. The pH
activity curve relative to V0 has a fairly broad pH optimum (pH 6.8-7.5):
measurements are made at pH 7.0. 5
Reagents
Phosphate buffer 50 mM, pH 7.0: dissolve (a) 6.81 g KH2POa, and (b)
8.90 g Na2HPO4 2H20 in distilled water and make up to 1000 ml
each. Mix solutions (a) and (b) in the proportion 1:1.5 (v/v)
Hydrogen peroxide 30 mM: dilute 0.34 ml 30% hydrogen peroxide
with phosphate buffer to I00 ml
Procedure
Measurement in Blood. Venous blood containing heparin or citrate is
centrifuged and the plasma and leukocyte layers are removed. The erythrocyte sediment is washed three times with isotonic NaCI. A stock hemolysate is prepared containing - 5 g Hb/100 ml by the addition of four parts
by volume of distilled water. A 1 500 dilution of this concentrated hemolysate is prepared with phosphate buffer immediately before the assay is
performed and Hb (hemoglobin) content is determined in duplicate (e.g.,
by the method of Drabkin). For capillary blood, 0. I or 0.02 ml is hemolyzed in 250 or 50 ml distilled water. If the hemoglobin content of the
blood is required as reference point, it must be determined in a separate
sample of blood. 6-8
M e a s u r e m e n t in Tissues. Catalase in tissues with relatively high activity, such as liver and kidney, can be determined spectrophotometrically if
complete lysis of all organelles and clear (or only slightly colored) solutions or extracts can be obtained. A detergent (e.g., 1% Triton X-100)
must be used in the preparation of the stock homogenate (1 + 9 or 1 + 19),
otherwise too low values will result. Further dilutions can be made with
phosphate buffer, pH 7.0 (I : 100 to 1 500, depending on tissue and species). However, if the sample after lysis of the organelles cannot be diluted to this extent, the considerable UV absorption of Triton X-I00 must
be kept in mind. As an alternative digitonin (0.01%) or sodium cholate
(0.25%) can be used. Normally, catalase activity of tissue samples is
expressed on a milligram wet weight or milligram total N basis. A conven-
B. Chance, H. Sies, and A. Boveris, Physiol. Rev. 59, 527 (1979).

6 H. Aebi, #~ "Exposes Annuels de Biochimie M~dicale," 29ieme s6rie, p. 139. Masson,
Paris, 1969.
7 H. Aebi and H. Suter, hi "BiochemicalMethods in Red Cell Genetics" (J. J. Yunis, ed,),
p. 255. Academic Press, New York, 1969.
8 H. Aebi, S. R. Wyss, B. Scherz, and J. Gross, Biochem. Genet. 14, 791 (1976).
124
[13]
ient method for the measurement of catalase activity in tissue extracts has
been described by Cohen et al. 9
Assay Conditions
Wavelength, 240 nm; light path, 10 mm; final volume, 3.00 mi. Read
the sample containing, 2.00 ml enzyme solution or hemolysate and 1 ml
H202 at 20 ( - room temperature) against a blank containing, 1 ml phosphate buffer instead of substrate and 2 ml enzyme solution or hemolysate.
The reaction is started by addition of H202. The initial absorbance should
be approximately A = 0.500. Mix well with a plastic paddle and follow the
decrease in absorbance with a recorder for about 30 sec.
Stability of Enzyme
Catalase in intact erythrocytes and in concentrated hemolysates is
stable up to 6 days when kept at 2. However, there is a relatively rapid
decline of activity in dilute hemolysates which is more likely due to decomposition of the enzyme into subunits than to proteolytic changes. At a
concentration of 1.2 mg Hb/ml the activity decreases by 10-15% within 24
hr; at a concentration of 0.06 mg Hb/ml the loss of activity is 10% after 1
hr and 80-90% after 24 hr. Consequently, hemolysate samples should be
analyzed within 5-10 min after dilution.
Definition of Units and Specific Activity

It is not possible to define international catalase units (U) according, to
IUB recommendations due to the abnormal kinetics. Therefore, the use of
a number of differently defined units and different methods of evaluation
is acceptable for this enzyme (a selection of methods is listed in the
table).~ Use of the rate constant of a first-order reaction (k) is recommended. The rate constant related to the hemoglobin content (k/g,Hb) can
serve as a measure of the specific activity of erythrocyte catalase. Equation (3) applies in this case. If the decrease in absorbance is recorded, the
value of log A tlA2 for a measured time interval or the time required for a
certain decrease in absorbance can be determined.
For a time interval of 15 sec the following, relationship is obtained
according, to Eq. (3):
k = (2.3/15)(1og AI/A2) = 0.153(1og, ALIA2)
(sec -I)
(5)
To calculate k/mi or k/g, Hb proceed as follows:

9 G. Cohen, D. Dembiec, and J. Marcus, Anal. Biochem. 34, 30 (1970).
~o H. Aebi, in "Methods of Enzymatic Analysis" (H. U. Bergmeyer, ed.), 3rd Ed. Verlag
Chemic, Weinheim, F. R. G., in preparation, 1983.
[13]
CATALASE in Vio'o
125
OTHER METHODS OF DETERMINATION
Method/technique
Determination of H202 removal
Titrimetric methods
Iodometric
Permanganometric
Spectrophotometry
Substrate: H202 (E240)
Substrate: perborate (E220)
Photometry (E405-E~15)
Vanadic acid
Titanium tetrachloride
Fluorimetry
Scopoletin
Diacetyldichlorofluorescein
Determination of 02 production
Oxygen electrode
Polarography
Catalase and SOD
Immunoprecipitation
(with anti-catalase)
Screening techniques
Capillary tube
"Siebtest"
Automated procedure
Technicon AutoAnalyzer
References
Material
Bonnichsen et al. ~
Bonnichsen3
Tissues, blood
Tissues, blood
Bergmeyer"
Cohen et al. 9
Thomson et al. ~2
Purified preparations
Tissues, organelles
Tissue fractions
Warburg and KrippahP

Pilz and Johannb
Cell cultures
Blood
Perschke and Brodac

Keston and Brandta
Aqueous
solutions
Ogata I~
Del Rio et al.'4
Meerhof and Roos j~
Blood
Plant material
Blood
Rigo and RotiliC 6

Higashi et al."
Ben-Yoseph and Shapira t~
Tissue homogenate
hemolysate
Blood, tissues
Blood
Fung and Petrishko f

Gross et al. 18
Microbial cultures
Blood
Lamy et al. 19
Leighton et al. 2
Blood
Tissue fractions
O. Warburg and G. Krippahl, Z. Naturforschung lllb, 340 (1963). b W. Pilz and J.

Johann, Z. Anal. Claem. 210, 358 (1965). ~ H. Perschke and E. Broda, N a t u r e {London) 190,
257 (1961). d A. S. Keston and R. Brandt, Anal. Biochem. 11, I (1965). "T. Higashi, M.
Yagi, and H. Hirai, J. Biochem. (Tokyo) 49, 707 (1961).f D. Y. C. Fung and D. T. Petrishko,
Appl. Microbiol. 26, 631 (1973).
k/ml = ka
k/g Hb = k/ml(lOOO/b) = (2.3/15)(a/b)(Iog AI/A2)
(sec -~)
(6)
(7)
where A~ is A240 at t = 0, A2 is A240 at t = 15 sec, a is the dilution factor [Hb

concentration in blood or erythrocyte sediment (mg Hb/ml)/Hb concentration in cuvette (rag Hb/ml)], and b is the Hb content of blood or erythrocyte sediment (grams/liter).
For the difference in absorbance of 0.450-0.400 (log AI/A2 = 0.05115)
the following relation holds:
k = (2.3/At)(log Aj/A2) = 0.1175/At
(sec -I)
(8)
126
[14]
Other Methods of Determination

This contribution deals only with the catalytic (not the peroxidic) activity of catalase. It can be measured by following either the decomposition of H202 or the liberation of 02. Accordingly, the remaining substrate
concentration at a given moment of the reaction can be determined by UV
spectrophotometry9,~'.~2 or--at the end of the reaction period--by simple
titration. 2,3 On the other hand, O~ production can be followed with the
oxygen electrode ~3-~5 or by polarography. ~6 Alternatively, catalase can
also be measured by immunoprecipitation. ~7 The method of choice for
biological material, however, is UV spectrophotometry. Titrimetric methods are suitable for comparative studies. For large series of measurements there are either simple screening tests which give a quick indication
of the approximative catalase activity, '8 or automated methods (e.g., using the Technicon AutoAnalyzer) available 19,2(see the table).
u H. U. Bergmeyer, Biochem. Z. 327~ 255 (1955).
t2 j. F. Thomson, S. L. Nance, and S. L. Tollaksen, Proc. Soc. Exp. Biol. Med. 157, 33
(1978).
,3 M. Ogata, in "Symposium on Genetics and Biochemistry of Acatalasemia" (IX Annual
Meeting of the Japan Society of Human Genetics), at Wakayama Medical College, 1964.
14 L. A. Del Rio et al., Anal. Biochem. 80, 409 (1977).
15 L. J. Meerhof and D. Roos, J. Reticuloendothel. Soc. 28, 419 (1980).
,6 A. Rigo and G. Rotilio, Anal. Biochem. 81, 157 (1977).
~7 y. Ben-Yoseph and E. Shapira, J. Lab. Clin. Med. 81, 133 (1973).
,8 j. Gross, A. Hartwig, and A. Golding, Z. Med. Labortech. 16, 336 (1975).
L9j. N. Lamy et al., Bull. Soc. Chim. Biol. 49, 1167 (1967).
20 F. Leighton et al., J. Cell Biol. 37, 482 (1968).
[14] Assays of L i p o x y g e n a s e , 1 , 4 - P e n t a d i e n e F a t t y Acids,

a n d 02 C o n c e n t r a t i o n s : C h e m i l u m i n e s c e n c e M e t h o d s
By SIMO LAAKSO, ESA-MATTI LILIUS, and PEKKATURUNEN

Lipoxygenases are iron-containing enzymes that catalyze the dioxygenation, by molecular oxygen, of cis,cis-1,4-pentadiene fatty acids. The
reaction is a source of weak chemiluminescence due to dissociation of
free radicals from the main path of hydroperoxidation.~ Under alkaline
conditions the intensity of light emission can be drastically amplified by
the presence of luminol? The kinetics of luminol chemiluminescence in
' A. Boveris, E. Cadenas, and B. Chance, Photobiochem. Photobiophys. 1, 175 0980).
2 E.-M. Lilius and S. Laakso, Anal. Biochem. 119, 135 (1982).
METHODS IN ENZYMOLOGY,VOL. 105
Copyright 1984by AcademicPress, Inc.

All rightsof reproductionin any form reserved.
ISBN 0-12-182005-X

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[13]

High concentrations of polyvalent anions, which may be contained in

Catalase exerts a dual function: (1) decomposition of H202 to give H20

METHODS IN ENZYMOLOGY, VOL. 105

Copyright 1984 by Academic Press. Inc.

FORMATION OR REMOVAL OF OXYGEN RADICALS

or determination of the Ks is therefore impossible. In contrast to reactions

where At = t2 - t~ = measured time interval and S~ and $2 = H202

(liters mol -l sec -l)

tion on the temperature is small (Qi0 - 1.1) so that measurements can be

B. Chance, H. Sies, and A. Boveris, Physiol. Rev. 59, 527 (1979).

FORMATION OR REMOVAL OF OXYGEN RADICALS

Definition of Units and Specific Activity

To calculate k/mi or k/g, Hb proceed as follows:

OTHER METHODS OF DETERMINATION

Warburg and KrippahP

Perschke and Brodac

Rigo and RotiliC 6

Fung and Petrishko f

O. Warburg and G. Krippahl, Z. Naturforschung lllb, 340 (1963). b W. Pilz and J.

where A~ is A240 at t = 0, A2 is A240 at t = 15 sec, a is the dilution factor [Hb

FORMATION OR REMOVAL OF OXYGEN RADICALS

Other Methods of Determination

[14] Assays of L i p o x y g e n a s e , 1 , 4 - P e n t a d i e n e F a t t y Acids,

By SIMO LAAKSO, ESA-MATTI LILIUS, and PEKKATURUNEN

METHODS IN ENZYMOLOGY,VOL. 105

Copyright 1984by AcademicPress, Inc.

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