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. Author manuscript; available in PMC: 2017 Mar 2.
Published in final edited form as: Chembiochem. 2016 Feb 4;17(5):394–397. doi: 10.1002/cbic.201500624

Table 1.

Activities and stereoselectivities of P450 variants for the reaction of styrene with ethyl diazoacetate.

graphic file with name nihms841851u1.jpg
Catalyst Yield TTN[a] dr [cis:trans] ee cis [%][b] ee trans [%][c]
hemin 16 79 13:87 −2 −4
P450BM3 1 7 12:88 0 −2
P450BM3-T268A 67 338 1:99 −18 −97
P450BM3-CIS-T438S 62 311 93:7 −97 −79
P450BioI 27 135 12:88 8 13
P450BioI-T238A 48 241 71:29 95 −24
P450cam 41 207 88:12 −43 9
P450cam-T252A 30 151 71:29 −86 −5
P450eryF (A245) 70 349 89:11 −99 −19
CYP142 49 246 44:56 −84 −6
CYP142-T234A 54 272 90:10 −97 −14
CYP164A2 7 34 14:85 5 2
CYP164A2-T260A 70 350 18:82 −82 −9
CYP107N1 7 36 9:91 0 −4
CYP107N1-T251A 48 238 9:91 −3 −3
P450nor 5 27 12:88 −6 −3
P450nor-T243A 13 66 10:90 −3 −2
P450EpoK 49 247 11:89 −15 −22
P450EpoK-T258A 44 219 18:82 −25 −14
P450PikC 50 249 8:92 −2 3
P450PikC-T247A 46 231 7:93 −15 32
P450RhF 52 258 9:91 −3 −2
P450RhF-T275A 34 171 12:88 −11 −2
P450TxtE 37 187 10:90 6 −2
P450TxtE-T250A 45 225 10:90 −2 −2
P450TylH1 48 242 13:87 16 8
P450TylH1-T279A 50 251 10:90 1 −28
[a]

TTN =total turnover number.

[b]

(1R,2S)–(1S,2R).

[c]

(1R,2R)–(1S,2S).

TTNs and stereoselectivities were determined by chiral GC analysis.