Detail
Článek
Článek online
FT
Medvik - BMČ
  • Je něco špatně v tomto záznamu ?

Cyanide hydratases and cyanide dihydratases: emerging tools in the biodegradation and biodetection of cyanide

L. Martínková, AB. Veselá, A. Rinágelová, M. Chmátal,

. 2015 ; 99 (21) : 8875-82. [pub] 20150902

Jazyk angličtina Země Německo

Typ dokumentu časopisecké články, práce podpořená grantem, přehledy

Perzistentní odkaz   https://www.medvik.cz/link/bmc16028260

The purpose of this study is to summarize the current knowledge of the enzymes which are involved in the hydrolysis of cyanide, i.e., cyanide hydratases (CHTs; EC 4.2.1.66) and cyanide dihydratases (CynD; EC 3.5.5.1). CHTs are probably exclusively produced by filamentous fungi and widely occur in these organisms; in contrast, CynDs were only found in a few bacterial genera. CHTs differ from CynDs in their reaction products (formamide vs. formic acid and ammonia, respectively). Several CHTs were also found to transform nitriles but with lower relative activities compared to HCN. Mutants of CynDs and CHTs were constructed to study the structure-activity relationships in these enzymes or to improve their catalytic properties. The effect of the C-terminal part of the protein on the enzyme activity was determined by constructing the corresponding deletion mutants. CynDs are less active at alkaline pH than CHTs. To improve its bioremediation potential, CynD from Bacillus pumilus was engineered by directed evolution combined with site-directed mutagenesis, and its operation at pH 10 was thus enabled. Some of the enzymes have been tested for their potential to eliminate cyanide from cyanide-containing wastewaters. CynDs were also used to construct cyanide biosensors.

Citace poskytuje Crossref.org

000      
00000naa a2200000 a 4500
001      
bmc16028260
003      
CZ-PrNML
005      
20161018120628.0
007      
ta
008      
161005s2015 gw f 000 0|eng||
009      
AR
024    7_
$a 10.1007/s00253-015-6899-0 $2 doi
024    7_
$a 10.1007/s00253-015-6899-0 $2 doi
035    __
$a (PubMed)26329848
040    __
$a ABA008 $b cze $d ABA008 $e AACR2
041    0_
$a eng
044    __
$a gw
100    1_
$a Martínková, Ludmila $u Laboratory of Biotransformation, Institute of Microbiology, Academy of Sciences of the Czech Republic, Vídeňská 1083, CZ-142 20, Prague, Czech Republic. martinko@biomed.cas.cz.
245    10
$a Cyanide hydratases and cyanide dihydratases: emerging tools in the biodegradation and biodetection of cyanide / $c L. Martínková, AB. Veselá, A. Rinágelová, M. Chmátal,
520    9_
$a The purpose of this study is to summarize the current knowledge of the enzymes which are involved in the hydrolysis of cyanide, i.e., cyanide hydratases (CHTs; EC 4.2.1.66) and cyanide dihydratases (CynD; EC 3.5.5.1). CHTs are probably exclusively produced by filamentous fungi and widely occur in these organisms; in contrast, CynDs were only found in a few bacterial genera. CHTs differ from CynDs in their reaction products (formamide vs. formic acid and ammonia, respectively). Several CHTs were also found to transform nitriles but with lower relative activities compared to HCN. Mutants of CynDs and CHTs were constructed to study the structure-activity relationships in these enzymes or to improve their catalytic properties. The effect of the C-terminal part of the protein on the enzyme activity was determined by constructing the corresponding deletion mutants. CynDs are less active at alkaline pH than CHTs. To improve its bioremediation potential, CynD from Bacillus pumilus was engineered by directed evolution combined with site-directed mutagenesis, and its operation at pH 10 was thus enabled. Some of the enzymes have been tested for their potential to eliminate cyanide from cyanide-containing wastewaters. CynDs were also used to construct cyanide biosensors.
650    _2
$a Bacteria $x enzymologie $7 D001419
650    12
$a biosenzitivní techniky $7 D015374
650    _2
$a biotransformace $7 D001711
650    _2
$a kyanidy $x analýza $x metabolismus $7 D003486
650    _2
$a mutační analýza DNA $7 D004252
650    _2
$a látky znečišťující životní prostředí $x analýza $x metabolismus $7 D004785
650    _2
$a stabilita enzymů $7 D004795
650    _2
$a houby $x enzymologie $7 D005658
650    _2
$a dehydratasy $x chemie $x genetika $x metabolismus $7 D006836
650    _2
$a koncentrace vodíkových iontů $7 D006863
650    _2
$a hydrolasy $x chemie $x genetika $x metabolismus $7 D006867
650    _2
$a hydrolýza $7 D006868
650    _2
$a mutantní proteiny $x genetika $x metabolismus $7 D050505
650    _2
$a proteinové inženýrství $7 D015202
650    _2
$a vztahy mezi strukturou a aktivitou $7 D013329
655    _2
$a časopisecké články $7 D016428
655    _2
$a práce podpořená grantem $7 D013485
655    _2
$a přehledy $7 D016454
700    1_
$a Veselá, Alicja Barbara $u Laboratory of Biotransformation, Institute of Microbiology, Academy of Sciences of the Czech Republic, Vídeňská 1083, CZ-142 20, Prague, Czech Republic. Department of Biochemistry, Charles University in Prague, Hlavova 8, CZ-128 40, Prague, Czech Republic.
700    1_
$a Rinágelová, Anna $u Laboratory of Biotransformation, Institute of Microbiology, Academy of Sciences of the Czech Republic, Vídeňská 1083, CZ-142 20, Prague, Czech Republic. Department of Biochemistry and Microbiology, University of Chemistry and Technology, Technická 3, CZ-166 28, Prague, Czech Republic.
700    1_
$a Chmátal, Martin $u Laboratory of Biotransformation, Institute of Microbiology, Academy of Sciences of the Czech Republic, Vídeňská 1083, CZ-142 20, Prague, Czech Republic.
773    0_
$w MED00000493 $t Applied microbiology and biotechnology $x 1432-0614 $g Roč. 99, č. 21 (2015), s. 8875-82
856    41
$u https://pubmed.ncbi.nlm.nih.gov/26329848 $y Pubmed
910    __
$a ABA008 $b sig $c sign $y a $z 0
990    __
$a 20161005 $b ABA008
991    __
$a 20161018121033 $b ABA008
999    __
$a ok $b bmc $g 1166574 $s 952890
BAS    __
$a 3
BAS    __
$a PreBMC
BMC    __
$a 2015 $b 99 $c 21 $d 8875-82 $e 20150902 $i 1432-0614 $m Applied microbiology and biotechnology $n Appl Microbiol Biotechnol $x MED00000493
LZP    __
$a Pubmed-20161005

Najít záznam

Citační ukazatele

Pouze přihlášení uživatelé

Možnosti archivace

Nahrávání dat ...