-
Je něco špatně v tomto záznamu ?
Oxidation of imidazole- and pyrazole-derived aldehydes by plant aldehyde dehydrogenases from the family 2 and 10
J. Frömmel, R. Končitíková, D. Kopečný, M. Soural, M. Šebela,
Jazyk angličtina Země Irsko
Typ dokumentu časopisecké články
- MeSH
- aldehyddehydrogenasa metabolismus MeSH
- aldehydy chemie metabolismus MeSH
- hrách setý enzymologie MeSH
- imidazoly chemie metabolismus MeSH
- kukuřice setá enzymologie MeSH
- molekulární struktura MeSH
- oxidace-redukce MeSH
- pyrazoly chemie metabolismus MeSH
- Solanum lycopersicum enzymologie MeSH
- Publikační typ
- časopisecké články MeSH
Plant cytosolic aldehyde dehydrogenases from family 2 (ALDH2s, EC 1.2.1.3) are non-specific enzymes and participate for example in the metabolism of acetaldehyde or biosynthesis of phenylpropanoids. Plant aminoaldehyde dehydrogenases (AMADHs, ALDH10 family, EC 1.2.1.19) are broadly specific and play an important role in polyamine degradation or production of osmoprotectants. We have tested imidazole and pyrazole carbaldehydes and their alkyl-, allyl-, benzyl-, phenyl-, pyrimidinyl- or thienyl-derivatives as possible substrates of plant ALDH2 and ALDH10 enzymes. Imidazole represents a building block of histidine, histamine as well as certain alkaloids. It also appears in synthetic pharmaceuticals such as imidazole antifungals. Biological compounds containing pyrazole are rare (e.g. pyrazole-1-alanine and pyrazofurin antibiotics) but the ring is often found as a constituent of many synthetic drugs and pesticides. The aim was to evaluate whether aldehyde compounds based on azole heterocycles are oxidized by the enzymes, which would further support their expected role as detoxifying aldehyde scavengers. The analyzed imidazole and pyrazole carbaldehydes were only slowly converted by ALDH10s but well oxidized by cytosolic maize ALDH2 isoforms (particularly by ALDH2C1). In the latter case, the respective Km values were in the range of 10-2000 μmol l-1; the kcat values appeared mostly between 0.1 and 1.0 s-1. The carbaldehyde group at the position 4 of imidazole was oxidized faster than that at the position 2. Such a difference was not observed for pyrazole carbaldehydes. Aldehydes with an aromatic substituent on their heterocyclic ring were oxidized faster than those with an aliphatic substituent. The most efficient of the tested substrates were comparable to benzaldehyde and p-anisaldehyde known as the best aromatic aldehyde substrates of plant cytosolic ALDH2s in vitro.
Citace poskytuje Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc19027812
- 003
- CZ-PrNML
- 005
- 20190823090704.0
- 007
- ta
- 008
- 190813s2019 ie f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.1016/j.cbi.2019.02.008 $2 doi
- 035 __
- $a (PubMed)30768969
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a ie
- 100 1_
- $a Frömmel, Jan $u Department of Protein Biochemistry and Proteomics, Centre of the Region Haná for Biotechnological and Agricultural Research, Faculty of Science, Palacký University, Šlechtitelů 27, 783 71, Olomouc, Czech Republic.
- 245 10
- $a Oxidation of imidazole- and pyrazole-derived aldehydes by plant aldehyde dehydrogenases from the family 2 and 10 / $c J. Frömmel, R. Končitíková, D. Kopečný, M. Soural, M. Šebela,
- 520 9_
- $a Plant cytosolic aldehyde dehydrogenases from family 2 (ALDH2s, EC 1.2.1.3) are non-specific enzymes and participate for example in the metabolism of acetaldehyde or biosynthesis of phenylpropanoids. Plant aminoaldehyde dehydrogenases (AMADHs, ALDH10 family, EC 1.2.1.19) are broadly specific and play an important role in polyamine degradation or production of osmoprotectants. We have tested imidazole and pyrazole carbaldehydes and their alkyl-, allyl-, benzyl-, phenyl-, pyrimidinyl- or thienyl-derivatives as possible substrates of plant ALDH2 and ALDH10 enzymes. Imidazole represents a building block of histidine, histamine as well as certain alkaloids. It also appears in synthetic pharmaceuticals such as imidazole antifungals. Biological compounds containing pyrazole are rare (e.g. pyrazole-1-alanine and pyrazofurin antibiotics) but the ring is often found as a constituent of many synthetic drugs and pesticides. The aim was to evaluate whether aldehyde compounds based on azole heterocycles are oxidized by the enzymes, which would further support their expected role as detoxifying aldehyde scavengers. The analyzed imidazole and pyrazole carbaldehydes were only slowly converted by ALDH10s but well oxidized by cytosolic maize ALDH2 isoforms (particularly by ALDH2C1). In the latter case, the respective Km values were in the range of 10-2000 μmol l-1; the kcat values appeared mostly between 0.1 and 1.0 s-1. The carbaldehyde group at the position 4 of imidazole was oxidized faster than that at the position 2. Such a difference was not observed for pyrazole carbaldehydes. Aldehydes with an aromatic substituent on their heterocyclic ring were oxidized faster than those with an aliphatic substituent. The most efficient of the tested substrates were comparable to benzaldehyde and p-anisaldehyde known as the best aromatic aldehyde substrates of plant cytosolic ALDH2s in vitro.
- 650 _2
- $a aldehyddehydrogenasa $x metabolismus $7 D000444
- 650 _2
- $a aldehydy $x chemie $x metabolismus $7 D000447
- 650 _2
- $a imidazoly $x chemie $x metabolismus $7 D007093
- 650 _2
- $a Solanum lycopersicum $x enzymologie $7 D018551
- 650 _2
- $a molekulární struktura $7 D015394
- 650 _2
- $a oxidace-redukce $7 D010084
- 650 _2
- $a hrách setý $x enzymologie $7 D018532
- 650 _2
- $a pyrazoly $x chemie $x metabolismus $7 D011720
- 650 _2
- $a kukuřice setá $x enzymologie $7 D003313
- 655 _2
- $a časopisecké články $7 D016428
- 700 1_
- $a Končitíková, Radka $u Department of Protein Biochemistry and Proteomics, Centre of the Region Haná for Biotechnological and Agricultural Research, Faculty of Science, Palacký University, Šlechtitelů 27, 783 71, Olomouc, Czech Republic.
- 700 1_
- $a Kopečný, David $u Department of Protein Biochemistry and Proteomics, Centre of the Region Haná for Biotechnological and Agricultural Research, Faculty of Science, Palacký University, Šlechtitelů 27, 783 71, Olomouc, Czech Republic. Electronic address: david.kopecny@upol.cz.
- 700 1_
- $a Soural, Miroslav $u Institute of Molecular and Translation Medicine, Faculty of Medicine and Dentistry, Palacký University, Hněvotínská 5, 779 00, Olomouc, Czech Republic.
- 700 1_
- $a Šebela, Marek $u Department of Protein Biochemistry and Proteomics, Centre of the Region Haná for Biotechnological and Agricultural Research, Faculty of Science, Palacký University, Šlechtitelů 27, 783 71, Olomouc, Czech Republic. Electronic address: marek.sebela@upol.cz.
- 773 0_
- $w MED00002111 $t Chemico-biological interactions $x 1872-7786 $g Roč. 304, č. - (2019), s. 194-201
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/30768969 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y a $z 0
- 990 __
- $a 20190813 $b ABA008
- 991 __
- $a 20190823090919 $b ABA008
- 999 __
- $a ok $b bmc $g 1432961 $s 1066272
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2019 $b 304 $c - $d 194-201 $e 20190213 $i 1872-7786 $m Chemico-biological interactions $n Chem Biol Interact $x MED00002111
- LZP __
- $a Pubmed-20190813