Utilization of recombinant pseudoazurin as an electron donor of nitrite reductase and follow-up measuring of dual enzymatic konetics.

KUŇÁK, Michal a Igor KUČERA. Utilization of recombinant pseudoazurin as an electron donor of nitrite reductase and follow-up measuring of dual enzymatic konetics. In Zborník XVIII.Biochemický zjazd. I. Bratislava: SAV Bratislava, 2002, s. 111-520. XVIII.biochemický zjazd.

Základní údaje

• Originální název: Utilization of recombinant pseudoazurin as an electron donor of nitrite reductase and follow-up measuring of dual enzymatic konetics.
• Název anglicky: Utilization of recombinant pseudoazurin as an electron donor of nitrite reductase and follow-up measuring of dual enzymatic konetics.
• Autoři: KUŇÁK, Michal a Igor KUČERA.
• Vydání: I. Bratislava, Zborník XVIII.Biochemický zjazd, s. 111-520, XVIII.biochemický zjazd, 2002.
• Nakladatel: SAV Bratislava

Další údaje

• Typ výsledku: Stať ve sborníku
• Utajení: není předmětem státního či obchodního tajemství
• Organizační jednotka: Přírodovědecká fakulta
• Klíčová slova anglicky: Paracoccus denitrification kinetics pseudoazurin
• Štítky: Paracoccus denitrification kinetics pseudoazurin

Anotace

Denitrification is an anaerobic respiratory process in which a nitrogen oxycompound serves as the electron acceptor. The key step of the whole denitrification pathway is the transformation of nitrite ion to gaseous nitric oxide. In the bacterium Paracoccus denitrificans this reaction is catalysed by nitrite reductase of the cytochrome cd1 type. The enzyme does not interact directly with membrane components but takes electrons from soluble periplasmic electron mediators (cytochrome c550 or pseudoazurin). Pseudoazurin in amount needed for konetics studies was obtained by procedure consisting of a PCR amplification of the pas gene, cloning in pRSET plasmid, overepression in E.coli DH5(and subsequent affinity chromatography (Ni-NTA Sepharose, fast flow, Qiagen)). Since P.denitrificans contains high concentration of nitrite reductase the enzyme could be isolated from wild strain of P.denitrificans. Activities of three different mediator proteins (horse cytochrome c, P. denitrificans cytochrome c550 and pseudoazurin) were compared by measuring the initial velocity of nitrite consumption in reconstituted systems containig membrane vesicles and nitrite reductase.

Anotace anglicky

Denitrification is an anaerobic respiratory process in which a nitrogen oxycompound serves as the electron acceptor. The key step of the whole denitrification pathway is the transformation of nitrite ion to gaseous nitric oxide. In the bacterium Paracoccus denitrificans this reaction is catalysed by nitrite reductase of the cytochrome cd1 type. The enzyme does not interact directly with membrane components but takes electrons from soluble periplasmic electron mediators (cytochrome c550 or pseudoazurin). Pseudoazurin in amount needed for konetics studies was obtained by procedure consisting of a PCR amplification of the pas gene, cloning in pRSET plasmid, overepression in E.coli DH5(and subsequent affinity chromatography (Ni-NTA Sepharose, fast flow, Qiagen)). Since P.denitrificans contains high concentration of nitrite reductase the enzyme could be isolated from wild strain of P.denitrificans. Activities of three different mediator proteins (horse cytochrome c, P. denitrificans cytochrome c550 and pseudoazurin) were compared by measuring the initial velocity of nitrite consumption in reconstituted systems containig membrane vesicles and nitrite reductase.