Latent and active abPPO4 mushroom tyrosinase cocrystallized with hexatungstotellurate(VI) in a single crystal. (1st September 2014)
- Record Type:
- Journal Article
- Title:
- Latent and active abPPO4 mushroom tyrosinase cocrystallized with hexatungstotellurate(VI) in a single crystal. (1st September 2014)
- Main Title:
- Latent and active abPPO4 mushroom tyrosinase cocrystallized with hexatungstotellurate(VI) in a single crystal
- Authors:
- Mauracher, Stephan Gerhard
Molitor, Christian
Al‐Oweini, Rami
Kortz, Ulrich
Rompel, Annette - Abstract:
- <abstract abstract-type="main" xml:lang="en"> <title> <x xml:space="preserve">Abstract</x> </title> <p>Tyrosinases, bifunctional metalloenzymes, catalyze the oxidation of monophenols and <italic>o</italic>‐diphenols to <italic>o</italic>‐quinones, the precursor compounds of the brown‐coloured pigment melanin. In eukaryotic organisms, tyrosinases are expressed as latent zymogens that have to be proteolytically cleaved in order to form highly active enzymes. This activation mechanism, known as the tyrosinase maturation process, has scientific and industrial significance with respect to biochemical and technical applications of the enzyme. Here, not only the first crystal structure of the mushroom tyrosinase <italic>ab</italic>PPO4 is presented in its active form (Ser2–Ser383) and in its 21 kDa heavier latent form (Ser2–Thr545), but furthermore the simultaneous presence of both forms within one single‐crystal structure is shown. This allows for a simple approach to investigate the transition between these two forms. Isoform <italic>ab</italic>PPO4 was isolated and extensively purified from the natural source (<italic>Agaricus bisporus</italic>), which contains a total of six polyphenol oxidases (PPOs). The enzyme formed crystals (diffracting to a resolution of 2.76 Å) owing to the employment of the 6‐tungstotellurate(VI) salt (Na<sub>6</sub>[TeW<sub>6</sub>O<sub>24</sub>]·22H<sub>2</sub>O) as a cocrystallization agent. Two of these disc‐shaped Anderson‐type polyoxoanions<abstract abstract-type="main" xml:lang="en"> <title> <x xml:space="preserve">Abstract</x> </title> <p>Tyrosinases, bifunctional metalloenzymes, catalyze the oxidation of monophenols and <italic>o</italic>‐diphenols to <italic>o</italic>‐quinones, the precursor compounds of the brown‐coloured pigment melanin. In eukaryotic organisms, tyrosinases are expressed as latent zymogens that have to be proteolytically cleaved in order to form highly active enzymes. This activation mechanism, known as the tyrosinase maturation process, has scientific and industrial significance with respect to biochemical and technical applications of the enzyme. Here, not only the first crystal structure of the mushroom tyrosinase <italic>ab</italic>PPO4 is presented in its active form (Ser2–Ser383) and in its 21 kDa heavier latent form (Ser2–Thr545), but furthermore the simultaneous presence of both forms within one single‐crystal structure is shown. This allows for a simple approach to investigate the transition between these two forms. Isoform <italic>ab</italic>PPO4 was isolated and extensively purified from the natural source (<italic>Agaricus bisporus</italic>), which contains a total of six polyphenol oxidases (PPOs). The enzyme formed crystals (diffracting to a resolution of 2.76 Å) owing to the employment of the 6‐tungstotellurate(VI) salt (Na<sub>6</sub>[TeW<sub>6</sub>O<sub>24</sub>]·22H<sub>2</sub>O) as a cocrystallization agent. Two of these disc‐shaped Anderson‐type polyoxoanions [TeW<sub>6</sub>O<sub>24</sub>]<sup>6−</sup> separate two asymmetric units comprising one crystallographic heterodimer of <italic>ab</italic>PPO4, thus resulting in very interesting crystal packing.</p> </abstract> … (more)
- Is Part Of:
- Acta crystallographica. Volume 70:Part 9(2014:Sep.)
- Journal:
- Acta crystallographica
- Issue:
- Volume 70:Part 9(2014:Sep.)
- Issue Display:
- Volume 70, Issue 9, Part 9 (2014)
- Year:
- 2014
- Volume:
- 70
- Issue:
- 9
- Part:
- 9
- Issue Sort Value:
- 2014-0070-0009-0009
- Page Start:
- 2301
- Page End:
- 2315
- Publication Date:
- 2014-09-01
- Subjects:
- Biomolecules -- Structure -- Periodicals
Physical biochemistry -- Periodicals
X-ray crystallography -- Periodicals
Crystallography -- Periodicals
572 - Journal URLs:
- http://firstsearch.oclc.org ↗
http://www.blackwell-synergy.com/loi/ayd ↗
http://www.blackwell-synergy.com/servlet/useragent?func=showIssues&code=ayd ↗
http://www.iucr.ac.uk/journals/acta/actad.html ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1107/S1399004714013777 ↗
- Languages:
- English
- ISSNs:
- 0907-4449
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 0612.022000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 2962.xml