Deazaflavins as mediators in light-driven cytochrome P450 catalyzed hydroxylations

Felipe E. Zilly; Andreas Taglieber; Frank Schulz; Frank Hollmann; Manfred T. Reetz

doi:10.1039/b913863c

journal article Jan 01, 2009

Deazaflavins as mediators in light-driven cytochrome P450 catalyzed hydroxylations

Felipe E. Zilly Andreas Taglieber Frank Schulz Frank Hollmann

Manfred T. Reetz

Chemical Communications No. 46 pp. 7152 · Royal Society of Chemistry (RSC)

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References

33

[1]

Narhi J. Biol. Chem. (1982) 10.1016/s0021-9258(18)34897-x

[2]

Wen J. Biol. Chem. (1987) 10.1016/s0021-9258(18)48295-6

[3]

Noble Biochem. J. (1999) 10.1042/bj3390371

[4]

Urlacher Trends Biotechnol. (2006) 10.1016/j.tibtech.2006.05.002

[5]

Julsing Curr. Opin. Chem. Biol. (2008) 10.1016/j.cbpa.2008.01.029

[6]

Maurer Adv. Synth. Catal. (2003) 10.1002/adsc.200303021

[7]

Wichmann Adv. Biochem. Eng. Biotechnol. (2005)

[8]

Zhao Curr. Opin. Biotechnol. (2003) 10.1016/j.copbio.2003.09.007

[9]

Schewe Appl. Microbiol. Biotechnol. (2008) 10.1007/s00253-007-1277-1

[10]

Schneider Appl. Environ. Microbiol. (1998) 10.1128/aem.64.10.3784-3790.1998

[11]

Schwaneberg J. Biomol. Screening (2001)

[12]

Chen Appl. Microbiol. Biotechnol. (2007) 10.1007/s00253-006-0811-x

[13]

Ni Biotechnol. Bioeng. (2004) 10.1002/bit.20202

[14]

Udit J. Inorg. Biochem. (2004) 10.1016/j.jinorgbio.2004.06.007

[15]

Hollmann J. Inorg. Biochem. (2009) 10.1016/j.jinorgbio.2008.11.005

[16]

Schwaneberg J. Biotechnol. (2000) 10.1016/s0168-1656(00)00357-6

[17]

Taglieber ChemBioChem (2008) 10.1002/cbic.200700435

[18]

Hollmann Angew. Chem., Int. Ed. (2007) 10.1002/anie.200605169

[19]

Frisell J. Biol. Chem. (1959) 10.1016/s0021-9258(18)98176-7

[20]

Massey J. Biol. Chem. (1994) 10.1016/s0021-9258(17)31664-2

[21]

Massey Biochemistry (1978) 10.1021/bi00594a002

[22]

Vermilion J. Biol. Chem. (1978) 10.1016/s0021-9258(17)34250-3

[23]

Peterson J. Biol. Chem. (1977) 10.1016/s0021-9258(17)40177-3

[24]

Shumyantseva Biosens. Bioelectron. (2002) 10.1016/s0956-5663(01)00181-6

[25]

Omura J. Biol. Chem. (1964) 10.1016/s0021-9258(20)82244-3

[26]

Boddupalli J. Biol. Chem. (1990) 10.1016/s0021-9258(19)39552-3

[27]

Girvan J. Am. Chem. Soc. (2007) 10.1021/ja071355m

[28]

Hollmann J. Am. Chem. Soc. (2005) 10.1021/ja050997b

[29]

Fang Drug Metab. Dispos. (1996) 10.1016/s0090-9556(25)08463-6

[30]

Cowart Arch. Biochem. Biophys. (2001) 10.1006/abbi.2000.2246

[31]

Faulkner Proc. Natl. Acad. Sci. U. S. A. (1995) 10.1073/pnas.92.17.7705

[32]

Shet Arch. Biochem. Biophys. (1995) 10.1006/abbi.1995.1235

[33]

Helvig Biochemistry (2000) 10.1021/bi992578v

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Published: Jan 01, 2009
Vol/Issue: (46)
Pages: 7152

Authors

Cite This Article

Felipe E. Zilly, Andreas Taglieber, Frank Schulz, et al. (2009). Deazaflavins as mediators in light-driven cytochrome P450 catalyzed hydroxylations. Chemical Communications(46), 7152. https://doi.org/10.1039/b913863c

Deazaflavins as mediators in light-driven cytochrome P450 catalyzed hydroxylations

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