Structural and functional characterization of an Isd‐type haem‐degradation enzyme from Listeria monocytogenes. (1st March 2014)
- Record Type:
- Journal Article
- Title:
- Structural and functional characterization of an Isd‐type haem‐degradation enzyme from Listeria monocytogenes. (1st March 2014)
- Main Title:
- Structural and functional characterization of an Isd‐type haem‐degradation enzyme from Listeria monocytogenes
- Authors:
- Duong, Thao
Park, Kwangsu
Kim, Truc
Kang, Sung Wook
Hahn, Myung Joon
Hwang, Hye‐Yeon
Kim, Kyeong Kyu - Abstract:
- <abstract abstract-type="main" xml:lang="en"> <title> <x xml:space="preserve">Abstract</x> </title> <p>Bacterial pathogens have evolved diverse types of efficient machinery to acquire haem, the most abundant source of iron in the human body, and degrade it for the utilization of iron. Gram‐positive bacteria commonly encode IsdG‐family proteins as haem‐degrading monooxygenases. <italic>Listeria monocytogenes</italic> is predicted to possess an IsdG‐type protein (Lmo2213), but the residues involved in haem monooxygenase activity are not well conserved and there is an extra N‐terminal domain in Lmo2213. Therefore, its function and mechanism of action cannot be predicted. In this study, the crystal structure of Lmo2213 was determined at 1.75 Å resolution and its haem‐binding and haem‐degradation activities were confirmed. Structure‐based mutational and functional assays of this protein, designated as an Isd‐type <italic>L. monocytogenes</italic> haem‐degrading enzyme (Isd‐LmHde), identified that Glu71, Tyr87 and Trp129 play important roles in haem degradation and that the N‐terminal domain is also critical for its haem‐degrading activity. The haem‐degradation product of Isd‐LmHde is verified to be biliverdin, which is also known to be the degradation product of other bacterial haem oxygenases. This study, the first structural and functional report of the haem‐degradation system in <italic>L. monocytogenes</italic>, sheds light on the concealed haem‐utilization system in this<abstract abstract-type="main" xml:lang="en"> <title> <x xml:space="preserve">Abstract</x> </title> <p>Bacterial pathogens have evolved diverse types of efficient machinery to acquire haem, the most abundant source of iron in the human body, and degrade it for the utilization of iron. Gram‐positive bacteria commonly encode IsdG‐family proteins as haem‐degrading monooxygenases. <italic>Listeria monocytogenes</italic> is predicted to possess an IsdG‐type protein (Lmo2213), but the residues involved in haem monooxygenase activity are not well conserved and there is an extra N‐terminal domain in Lmo2213. Therefore, its function and mechanism of action cannot be predicted. In this study, the crystal structure of Lmo2213 was determined at 1.75 Å resolution and its haem‐binding and haem‐degradation activities were confirmed. Structure‐based mutational and functional assays of this protein, designated as an Isd‐type <italic>L. monocytogenes</italic> haem‐degrading enzyme (Isd‐LmHde), identified that Glu71, Tyr87 and Trp129 play important roles in haem degradation and that the N‐terminal domain is also critical for its haem‐degrading activity. The haem‐degradation product of Isd‐LmHde is verified to be biliverdin, which is also known to be the degradation product of other bacterial haem oxygenases. This study, the first structural and functional report of the haem‐degradation system in <italic>L. monocytogenes</italic>, sheds light on the concealed haem‐utilization system in this life‐threatening human pathogen.</p> </abstract> … (more)
- Is Part Of:
- Acta crystallographica. Volume 70:Part 3(2014:Mar.)
- Journal:
- Acta crystallographica
- Issue:
- Volume 70:Part 3(2014:Mar.)
- Issue Display:
- Volume 70, Issue 3, Part 3 (2014)
- Year:
- 2014
- Volume:
- 70
- Issue:
- 3
- Part:
- 3
- Issue Sort Value:
- 2014-0070-0003-0003
- Page Start:
- 615
- Page End:
- 626
- Publication Date:
- 2014-03-01
- 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/S1399004713030794 ↗
- 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:
- 3787.xml