Substrate promiscuity of cytochrome P450 RhFCitation formats

  • External authors:
  • Elaine O'Reilly
  • Mark Corbett
  • Shahed Hussain
  • Paul P. Kelly
  • Dominique Richardson

Standard

Substrate promiscuity of cytochrome P450 RhF. / O'Reilly, Elaine; Corbett, Mark; Hussain, Shahed; Kelly, Paul P.; Richardson, Dominique; Flitsch, Sabine L.; Turner, Nicholas J.

In: Catalysis Science and Technology, Vol. 3, No. 6, 06.2013, p. 1490-1492.

Research output: Contribution to journalArticle

Harvard

O'Reilly, E, Corbett, M, Hussain, S, Kelly, PP, Richardson, D, Flitsch, SL & Turner, NJ 2013, 'Substrate promiscuity of cytochrome P450 RhF', Catalysis Science and Technology, vol. 3, no. 6, pp. 1490-1492. https://doi.org/10.1039/c3cy00091e

APA

O'Reilly, E., Corbett, M., Hussain, S., Kelly, P. P., Richardson, D., Flitsch, S. L., & Turner, N. J. (2013). Substrate promiscuity of cytochrome P450 RhF. Catalysis Science and Technology, 3(6), 1490-1492. https://doi.org/10.1039/c3cy00091e

Vancouver

O'Reilly E, Corbett M, Hussain S, Kelly PP, Richardson D, Flitsch SL et al. Substrate promiscuity of cytochrome P450 RhF. Catalysis Science and Technology. 2013 Jun;3(6):1490-1492. https://doi.org/10.1039/c3cy00091e

Author

O'Reilly, Elaine ; Corbett, Mark ; Hussain, Shahed ; Kelly, Paul P. ; Richardson, Dominique ; Flitsch, Sabine L. ; Turner, Nicholas J. / Substrate promiscuity of cytochrome P450 RhF. In: Catalysis Science and Technology. 2013 ; Vol. 3, No. 6. pp. 1490-1492.

Bibtex

@article{f1ac0a931a4743a38ae2d3727b4c3b25,
title = "Substrate promiscuity of cytochrome P450 RhF",
abstract = "Cytochrome P450 RhF displays a high degree of substrate promiscuity, mediating a range of O-dealkylations, aromatic hydroxylations, epoxidations and asymmetric sulfoxidations. The self-sufficient nature of this CYP coupled with its ability to catalyse the oxidation of a wide range of functional groups highlights this enzyme as an excellent starting template for directed evolution and promising alternate to P450 BM3. {\circledC} 2013 The Royal Society of Chemistry.",
author = "Elaine O'Reilly and Mark Corbett and Shahed Hussain and Kelly, {Paul P.} and Dominique Richardson and Flitsch, {Sabine L.} and Turner, {Nicholas J.}",
year = "2013",
month = "6",
doi = "10.1039/c3cy00091e",
language = "English",
volume = "3",
pages = "1490--1492",
journal = "Catalysis Science and Technology",
issn = "2044-4753",
publisher = "Royal Society of Chemistry",
number = "6",

}

RIS

TY - JOUR

T1 - Substrate promiscuity of cytochrome P450 RhF

AU - O'Reilly, Elaine

AU - Corbett, Mark

AU - Hussain, Shahed

AU - Kelly, Paul P.

AU - Richardson, Dominique

AU - Flitsch, Sabine L.

AU - Turner, Nicholas J.

PY - 2013/6

Y1 - 2013/6

N2 - Cytochrome P450 RhF displays a high degree of substrate promiscuity, mediating a range of O-dealkylations, aromatic hydroxylations, epoxidations and asymmetric sulfoxidations. The self-sufficient nature of this CYP coupled with its ability to catalyse the oxidation of a wide range of functional groups highlights this enzyme as an excellent starting template for directed evolution and promising alternate to P450 BM3. © 2013 The Royal Society of Chemistry.

AB - Cytochrome P450 RhF displays a high degree of substrate promiscuity, mediating a range of O-dealkylations, aromatic hydroxylations, epoxidations and asymmetric sulfoxidations. The self-sufficient nature of this CYP coupled with its ability to catalyse the oxidation of a wide range of functional groups highlights this enzyme as an excellent starting template for directed evolution and promising alternate to P450 BM3. © 2013 The Royal Society of Chemistry.

U2 - 10.1039/c3cy00091e

DO - 10.1039/c3cy00091e

M3 - Article

VL - 3

SP - 1490

EP - 1492

JO - Catalysis Science and Technology

JF - Catalysis Science and Technology

SN - 2044-4753

IS - 6

ER -