Part:BBa_K316003

XylE - catechol 2,3-dioxygenase from P.putida with terminator

Catechol or catechol 2,3-dioxygenases + O(2) is converted by a ring cleavage into 2-hydroxymuconate semialdehyde which is the toxic and bright yellow-coloured substrate1. This is a key enzyme in many (soil) bacterial species used for the degradation of aromatic compounds. Catechol 2,3-dioxygenase (pdb id: 1MPY2[http://www.ebi.ac.uk/pdbsum/1mpy]) was originally isolated from Pseudomonas putida and is a homotetramer of C230 monomers. The tetramerization interactions position a ferrous ion critical for enzymatic activity. It has been deduced that intersubunit interaction is essential to produce a functioning enzyme after performing N and C terminal modifications on the monomer. Coming together the subunits generate an active site. The reaction itself takes place within seconds after the addition by Pasteur pipette or spraying of catechol at a 100mM stock solution diluted with DDH20 (used by our lab.) The toxic byproduct is thought to interfere with cell wall integrity and cellular machinery such that exposed cells gradually die.

Please see ‘Part Design’ section for design considerations and parts used.

Sequence and Features

Assembly Compatibility:

• 10
  COMPATIBLE WITH RFC[10]
• 12
  COMPATIBLE WITH RFC[12]
• 21
  COMPATIBLE WITH RFC[21]
• 23
  COMPATIBLE WITH RFC[23]
• 25
  INCOMPATIBLE WITH RFC[25]

  Illegal NgoMIV site found at 337
  Illegal NgoMIV site found at 509
  Illegal AgeI site found at 860
  
• 1000
  COMPATIBLE WITH RFC[1000]

Part Characterisation

Characterisation data still to come

References

<biblio>

1. 1 pmid=10368270
2. 2 http://www.ebi.ac.uk/pdbsum/1mpy

Biochem. J. (2003) 371, 557–564 (Printed in Great Britain) 557 Intersubunit interaction and catalytic activity of catechol 2,3-dioxygenases Akiko OKUTA1, Kouhei OHNISHI2,3, Sakiko YAGAME and Shigeaki HARAYAMA Marine Biotechnology Institute, 3-75-1 Heita, Kamaishi, Iwate 026-0001, Japan

</biblio>