Catalase (
CAT) is converted by decomposition and intracellular localization relationships of the
main cellular
antioxidant enzyme system like
superoxide dismutase (
SOD),
peroxiredoxins (
Prdx), and
glutathione peroxidase (
GPX) are peroxisomal matrix enzymes in the cytoplasm,
translocated to the peroxisomes to catalyze hydrogen peroxide
H2O2 which is
decomposed to oxygen and water, locus:
11p13 (
§,
‡). Unlike catalase, the objective of this communication, SOD which
prevents the formation of
Hydroxyl radicals – (
HRGT) determined from constant of
O2.- dismutation, and generation of reversibly inactive (CAT)-compound II,
Panax ginseng could induce both transcription factors. Catalase is composed of four identical subunits each of the subunits binds one heme-containing active site, and produces two catalase
compounds HPI and HPII (PDB:
1p80) is flipped
180 degrees » with respect to the orientation of the heme related to the « root mean square to the
structure of catalase, (Mutation
Location) from peroxisomal catalases inactive state in compound II NADP+(H) binding pockets inverted remains similar to the structure of the wild type (Val111, PDB:
1A4E, KatG) orientation on the heme
proximal (PDB: 1GGK) side,
inactivate catalase can be prevented by
melatonin. Catalase (CAT; EC
1.11.1.6) a free radical scavenging enzyme (
FRSE) is a scavenger of
H2O2. Protoporphyrin – (ZnPPIX) (PDB:
1H6N), from a heme group of the ‘heme-pathway, which forms catalase,’ is a scavenger of
antioxidant (
HO-1-HMOX1)
heme oxygenase, involving
ROS. Catalase is part of the enzymatic defense
system constituting the
primary defense against
ROS, zinc protoporphyrin IX (
ZnPPIX) is an inhibitor of (HO-1) heme oxygenase. Catalase
protects the cell from oxidative
damage by the accumulation of cellular reactive oxygen species (
ROS) generation systems, those
peroxisomal enzymes that
breaks down hydrogen peroxide after H(2)O(2) exposure, and thereby
mitigates* (some
contradictory* results) the toxic effects of hydrogen peroxide. In the process (The typical hydroperoxidases (CAT) known as
Compound I) of the substrate of catalase,
NADP+ (an
inactive state,
compound II) is replaced by another molecule of NADP(H) to provide protection of catalase against
inactivation by (H2O2) hydrogen peroxide.
Erythrocyte [Human erythrocyte catalase (
HEC), The
NADPH-binding sites were empty – PDB: 1F4J,
1QQW] and plasma
indices (enzymatic-
antioxidants) initially implies the thiobarbituric acid-reacting substances (
TBARS) based on reaction with hydroxyl radicals (
OH) can release thiobarbituric acid,
TBAR inhibition
measures malondialdehyde (
MDA – impact of coenzyme
Q10) correlated (with MPO-myeloperoxidase
activity -generating ROS) as
co-variable, by which
mulberry leaf polysaccharide (MLPII) via the decomposition of (certain)
MDA, products of
lipid peroxidation (
LPO) were reduced. Comparisons were to specific activities of catalase (
SNP) single nucleotide
polymorphisms (CAT-C-
262 (rs
1001179) the low-risk
allele) of genetic variants in both, promoter a common
C/T polymorphism (
262-C/
T), and in
nine –
exonic – regions and its boundaries, occur frequently associated distally in
genomic mutations, similar to those of
normal catalase demonstrating
changes in catalase protein level targeted to the peroxisomal
matrix. The 262-C/T CAT low-risk allele is hypothetically related to the lower risk variant allele CAT
Tyr308 G to A point mutation ineducable in the Japanese acatalasemia allele. The common C/T polymorphism can be
targeted by dietary
and/or pharmacological antioxidants, and the
endogenous antioxidant defense
enzymes concentration can prevent cellular
lipid (
LPO)
peroxidative reactions occurring. Catalase is a homo
tetramer complex of 4 identical
monofunctional subunits. Catalase is located at the
peroxisome of human cells associated with several (
PBDs)-
peroxisomal biogenesis disorders commonly caused by mutations in the PEX
genes, peroxisomal targeting signal 1 (
PTS1) protein affecting in peroxisomal
biogenesis, the monomeric to homotetrameric transition in the forms of peroxisome
biogenesis disorder. PBDs also include
Acatalasemia the only disease
known to be caused by the (CAT) gene. In human catalase, the antioxidant
heme enzyme, is localized in the cytoplasm to the
peroxisome, nucleus, or
linked with mitochondria which in most cells
lack catalase (
Peroxisomes do not contain
DNA), its
mitochondrial fraction (microperoxisome), a secondary
phenomena shows physiological decline,
aging and age-
related reactions in
mitochondrial function and
disfunction.
NADPH is required for the prevention of forming an
inactive state of the enzyme. Antioxidative defence mechanisms, capacity and redox cycle enzyme activities increasing with Tc treatment
Tinospora cordifolia (Tc), T and B cells and antibody. Both
RBCs and plasma were measured on parameters of oxidative stress.
Syzygium cumini aqueous leaves extract (ASc) was able to remove oxidant species in a hyperglycemic state generated in red blood cells RBC-CAT levels. Catalase alone is unable to prevent in a hyperglycemic state.
Macrophages recruit other types of immune cells such as lymphocytes white blood cells (
WBCs). Catalase is dependent on the family of
NADPH-binding catalases for function, the prevention and reversal of inactivation by its toxic substrate (H2O2) hydrogen peroxide. Amyloid-
beta binds catalase and
inhibits (
H2O2) hydrogen peroxide, a reactive oxygen species,
breakdown through efficient
dismutation, and malonaldelhyde (MDA) determined in
plasma, as well as another member of the oxidoreductase family, myeloperoxidase (
MPO (EC
1.11.1.7)) converting H(2)O(2), the reducing equivalents produces (
HOCl) hypochlorous acid a
mechanism of cell-mediated antimicrobial immune defense for
monofunctional catalases one of three subgroups related to catalase deficiency in humans, in micro-organisms
manganese-containing catalases (‘large catalases’) determining in part the bifunctional activity of (
KatG, PDB:
1X7U) represented by
bifunctional (
heme)
catalase-peroxidase based Bacterial-
resistance mechanisms. Peroxiredoxins (Prxs, EC
1.11.1.21),
bifunctional catalase-peroxidases (
KatGs) two
organelle systems are antioxidant enzymes of the peroxiredoxin family that oxidize and reduce H(2)O(2) hydrogen peroxide thereby modulating the
catalase reaction, KatGs are
not found in plants and animals. Trx (
thioredoxin) a
redox-regulating protein also
controls the antioxidant enzyme activity of the main cellular antioxidant enzymes (
AOE) superoxide dismutase (SOD) and catalase.
The function of
NADPH bound to
Catalase.

The cytosine to thymidine transition of nucleotide-262 (-262C>T) Computer analysis indicated that the two variants bound promoter the Ile (-262 C/T) and (B)
Ile-262 in the
5′-flanking region carrying the T allele best captured and characterized the generation of the hydroxyl radical site in (PDB:
1DGB), (CAT) -[GLU]
330C>T transition, is known also as -262C>T. The ‘T allele in comparison to the C allele’ is a common C/T polymorphism frequency in the
promoter region association was observed between genotypes for locus11p13 risk alleles acatalasemia mutation Asp (
37C>T in exon 9) was hypothetically related to the lower risk Japanese acatalasemia allele
Tyr308 a single
G to
A (see: rs
7947841 to evaluate the link to rs
769214) point mutation ineducable or near exon 9 (
TC, CC, TT) of the CAT gene to which variant changes in the promoter region C/T-262 polymorphism are more closely related to CAT T/C at codon
389 in exon 9 (rs
769217)
polymorphism did not
differ significantly from those of healthy
controls in both promoter (-262 C/T) and in exonic (
ASP–
389 C/T) regions of the catalase (
CAT).
Tyr 370 resolves the 25 A-long (hydrogen peroxide) channel a constriction or narrowing of the channel leading to the heme cavity (‘Parameters) situated in the entrance channel to a heme protoporphyrin (ZnPPIX) (PDB: 1H6N) from a heme group, capable of heme
biosynthesis‘ in a wide range of organisms convert it into into
heme b, protoporphyrin
IX-heme. Two channels lead close to the distal side. A third channel reaching the heme
proximal side Tyr 370,
Ile-262 is proposed as a the ‘PDB: 1DGB – variant with a substituted residue in the ASP 178 to the (Met)
D181E variant PDB
1p80‘. These differences include the structure of the variant protein
Val111Ala (Saccharomyces cerevisiae) related supports the existence of the ‘Heme and NADP(H) binding pockets’. The omission of a 20-residue PDB: 1F4J, (1QQW) segment corresponds to the N-terminal (blue) of catalase from human erythrocytes (HEC), or in a
C-terminal (red) domain organized with an extra
flavodoxin-like
fold topology may provide with weak coordination the
N- or C-terminal, that allows scrutiny of the origins (topology) in this report of what would otherwise remain speculative or
determined with further verification.
Biological Xenobiotic Extracts Applications of note In the presence of Catalase:
green tea polyphenol (-)-epigallocatechin-3-gallate (EGCG)
Yamamoto T, Lewis J, Wataha J, Dickinson D, Singh B, Bollag WB, Ueta E, OsakiT, Athar M, Schuster G, Hsu S. Roles of catalase and hydrogen peroxide in greentea polyphenol-induced chemopreventive effects. J Pharmacol Exp Ther. 2004Jan;308(1):317-23. Epub 2003 Oct 20. PubMed PMID: 14569057.Furukawa A, Oikawa S, Murata M, Hiraku Y, Kawanishi S. (-)-Epigallocatechingallate causes oxidative damage to isolated and cellular DNA. Biochem Pharmacol.2003 Nov 1;66(9):1769-78. PubMed PMID: 14563487.*
Trigonella (Fenugreek)
Mohammad S, Taha A, Bamezai RN, Basir SF, Baquer NZ. Lower doses of vanadatein combination with trigonella restore altered carbohydrate metabolism andantioxidant status in alloxan-diabetic rats. Clin Chim Acta. 2004Apr;342(1-2):105-14. Erratum in: Clin Chim Acta. 2010 Aug 5;411(15-16):1158.Mohamad, Sameer [corrected to Mohammad, Sameer]. PubMed PMID: 15026271.
Aegle marmelos
Khan TH, Sultana S. Antioxidant and hepatoprotective potential of Aeglemarmelos Correa. against CCl4-induced oxidative stress and early tumor events. JEnzyme Inhib Med Chem. 2009 Apr;24(2):320-7. doi: 10.1080/14756360802167754 .PubMed PMID: 18830880.
Centella asiatica
Flora SJ, Gupta R. Beneficial effects of Centella asiatica aqueous extractagainst arsenic-induced oxidative stress and essential metal status in rats.Phytother Res. 2007 Oct;21(10):980-8. PubMed PMID: 17600859.
Daidzein
Mishra P, Kar A, Kale RK. Prevention of chemically induced mammarytumorigenesis by daidzein in pre-pubertal rats: the role of peroxidative damageand antioxidative enzymes. Mol Cell Biochem. 2009 May;325(1-2):149-57. doi:10.1007/s11010-009-0029-1. Epub 2009 Feb 13. PubMed PMID: 19214712.
Capparis
Yadav P, Sarkar S, Bhatnagar D. Action of capparis decidua againstalloxan-induced oxidative stress and diabetes in rat tissues. Pharmacol Res. 1997Sep;36(3):221-8. PubMed PMID: 9367667.
Retinal
Kannan R, Jin M, Gamulescu MA, Hinton DR. Ceramide-induced apoptosis: role ofcatalase and hepatocyte growth factor. Free Radic Biol Med. 2004 Jul15;37(2):166-75. PubMed PMID: 15203188.
Retinol
Cemek M, Caksen H, Bayiroğlu F, Cemek F, Dede S. Oxidative stress andenzymic-non-enzymic antioxidant responses in children with acute pneumonia. CellBiochem Funct. 2006 May-Jun;24(3):269-73. PubMed PMID: 16634091.
Diallyl disulfide (Allicin)
Kalayarasan S, Prabhu PN, Sriram N, Manikandan R, Arumugam M, Sudhandiran G.Diallyl sulfide enhances antioxidants and inhibits inflammation through theactivation of Nrf2 against gentamicin-induced nephrotoxicity in Wistar rats. EurJ Pharmacol. 2009 Mar 15;606(1-3):162-71. doi: 10.1016/j.ejphar.2008.12.055. Epub2009 Jan 19. PubMed PMID: 19374873.
Leucas aspera (Catechin, EGCG)
Kripa KG, Chamundeeswari D, Thanka J, Uma Maheswara Reddy C. Modulation ofinflammatory markers by the ethanolic extract of Leucas aspera in adjuvantarthritis. J Ethnopharmacol. 2011 Apr 12;134(3):1024-7. doi:10.1016/j.jep.2011.01.010. Epub 2011 Jan 18. PubMed PMID: 21251972.
Urtica dioica (nettle suppliment)Ozen T, Korkmaz H. Modulatory effect of Urtica dioica L. (Urticaceae) leaf
extract on biotransformation enzyme systems, antioxidant enzymes, lactatedehydrogenase and lipid peroxidation in mice. Phytomedicine. 2003;10(5):405-15.PubMed PMID: 12834006.
Justicia adhatoda
Singh RP, Padmavathi B, Rao AR. Modulatory influence of Adhatoda vesica(Justicia adhatoda) leaf extract on the enzymes of xenobiotic metabolism,antioxidant status and lipid peroxidation in mice. Mol Cell Biochem. 2000Oct;213(1-2):99-109. PubMed PMID: 11129964.
Phyllanthus niruri L. (Euphorbiaceae) (P. niruri)
Bhattacharjee R, Sil PC. Protein isolate from the herb, Phyllanthus niruri L.(Euphorbiaceae), plays hepatoprotective role against carbon tetrachloride inducedliver damage via its antioxidant properties. Food Chem Toxicol. 2007May;45(5):817-26. Epub 2006 Nov 11. PubMed PMID: 17175085.
Tinospora cordifolia
Sharma V, Pandey D. Protective Role of Tinospora cordifolia againstLead-induced Hepatotoxicity. Toxicol Int. 2010 Jan;17(1):12-7. doi:10.4103/0971-6580.68343. PubMed PMID: 21042467; PubMed Central PMCID: PMC2964743.
Aher V, Kumar Wahi A. Biotechnological Approach to Evaluate theImmunomodulatory Activity of Ethanolic Extract of Tinospora cordifolia Stem(Mango Plant Climber). Iran J Pharm Res. 2012 Summer;11(3):863-72. PubMed PMID:24250513; PubMed Central PMCID: PMC3813135.
coenzyme Q10
Lee BJ, Lin YC, Huang YC, Ko YW, Hsia S, Lin PT. The relationship betweencoenzyme Q10, oxidative stress, and antioxidant enzymes activities and coronaryartery disease. ScientificWorldJournal. 2012;2012:792756. doi:10.1100/2012/792756. Epub 2012 May 3. PubMed PMID: 22645453; PubMed CentralPMCID: PMC3356738.
Dietary carotenoid-rich pequi oil
Miranda-Vilela AL, Akimoto AK, Alves PC, Pereira LC, Gonçalves CA,Klautau-Guimarães MN, Grisolia CK. Dietary carotenoid-rich pequi oil reducesplasma lipid peroxidation and DNA damage in runners and evidence for anassociation with MnSOD genetic variant -Val9Ala. Genet Mol Res. 2009 Dec15;8(4):1481-95. doi: 10.4238/vol8-4gmr684. PubMed PMID: 20082261.
Tinospora cordifolia (Mango Plant Climber) extract from Tinospora known as Tinofend Aher V, Kumar Wahi A. Biotechnological Approach to Evaluate theImmunomodulatory Activity of Ethanolic Extract of Tinospora cordifolia Stem(Mango Plant Climber). Iran J Pharm Res. 2012 Summer;11(3):863-72. PubMed PMID:24250513; PubMed Central PMCID: PMC3813135.
mulberry leaf polysaccharide (MLPII)
Ren C, Zhang Y, Cui W, Lu G, Wang Y, Gao H, Huang L, Mu Z. A polysaccharideextract of mulberry leaf ameliorates hepatic glucose metabolism and insulinsignaling in rats with type 2 diabetes induced by high fat-diet andstreptozotocin. Int J Biol Macromol. 2014 Oct 11. pii: S0141-8130(14)00674-6.doi: 10.1016/j.ijbiomac.2014.09.060. [Epub ahead of print] PubMed PMID: 25316427.
five widely studied medicinal plants (Protandim)
Nelson SK, Bose SK, Grunwald GK, Myhill P, McCord JM. The induction of humansuperoxide dismutase and catalase in vivo: a fundamentally new approach toantioxidant therapy. Free Radic Biol Med. 2006 Jan 15;40(2):341-7. PubMed PMID:16413416.
melatonin
Mayo JC, Tan DX, Sainz RM, Lopez-Burillo S, Reiter RJ. Oxidative damage tocatalase induced by peroxyl radicals: functional protection by melatonin andother antioxidants. Free Radic Res. 2003 May;37(5):543-53. PubMed PMID: 12797476.
Protective effect of harmaline
Kim DH, Jang YY, Han ES, Lee CS. Protective effect of harmaline and harmalolagainst dopamine- and 6-hydroxydopamine-induced oxidative damage of brainmitochondria and synaptosomes, and viability loss of PC12 cells. Eur J Neurosci.2001 May;13(10):1861-72. PubMed PMID: 11403679.
horseradish peroxidase (HRP)
Shen L, Hu N. Heme protein films with polyamidoamine dendrimer: directelectrochemistry and electrocatalysis. Biochim Biophys Acta. 2004 Jan30;1608(1):23-33. PubMed PMID: 14741582.
Selegiline (–)Deprenyl
Kitani K, Minami C, Isobe K, Maehara K, Kanai S, Ivy GO, Carrillo MC. Why(–)deprenyl prolongs survivals of experimental animals: increase of anti-oxidantenzymes in brain and other body tissues as well as mobilization of varioushumoral factors may lead to systemic anti-aging effects. Mech Ageing Dev. 2002Apr 30;123(8):1087-100. Review. PubMed PMID: 12044958.
Rhodiola rosea
Bayliak MM, Lushchak VI. The golden root, Rhodiola rosea, prolongs lifespanbut decreases oxidative stress resistance in yeast Saccharomyces cerevisiae.Phytomedicine. 2011 Nov 15;18(14):1262-8. doi: 10.1016/j.phymed.2011.06.010. Epub2011 Jul 30. PubMed PMID: 21802922.
Carnitine
Kiziltunc A, Coğalgil S, Cerrahoğlu L. Carnitine and antioxidants levels inpatients with rheumatoid arthritis. Scand J Rheumatol. 1998;27(6):441-5. PubMedPMID: 9855215.
Syzygium cumini
De Bona KS, Bellé LP, Sari MH, Thomé G, Schetinger MR, Morsch VM, Boligon A,
Athayde ML, Pigatto AS, Moretto MB. Syzygium cumini extract decrease adenosine
deaminase, 5’nucleotidase activities and oxidative damage in platelets of
diabetic patients. Cell Physiol Biochem. 2010;26(4-5):729-38. doi:
10.1159/000322340. Epub 2010 Oct 29. PubMed PMID: 21063110.