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Industrial Biotransformations

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Transaminase<br />

Bacillus megaterium<br />

1) Reaction conditions<br />

[2]: 0.7 M, 61.7 g · L –1 [88.11 g · mol –1 ]<br />

medium: aqueous<br />

reaction type: amino group transfer<br />

catalyst: suspended whole cells<br />

enzyme: aminotransferase (transaminase)<br />

strain: Bacillus megaterium<br />

2) Remarks<br />

O<br />

1 = 1-methoxy-propan-2-one<br />

2 = isopropylamine<br />

3 = methoxy isopropylamine<br />

4 = acetone<br />

Fig. 2.6.1.X – 1<br />

● Isopropylamine is the choice for the amino donor because it is a cheap and a kinetically attractive<br />

molecule.<br />

● Main disadvantage of the wild-type transaminase is that the conversion is limited due to product<br />

inhibition.<br />

● Starting with the wild-type transaminase, the gene encoding the enzyme could be optimized<br />

step by step by mutation.<br />

● A single mutation in the gene coding the transaminase increases the possible product concentration<br />

from 0.16 M to 0.45 M.<br />

● The screening criteria for better genes included, beside higher inhibitor concentrations, better<br />

reaction rates, higher stability and lower K M-values.<br />

● Since no recycling of the catalyst is integrated, the residual activity after one batch run is of no<br />

interest.<br />

3) Flow scheme<br />

Not published.<br />

E<br />

O NH2 NH2 + O<br />

+<br />

1 (R/S)-2 (S)-3 4<br />

O<br />

EC 2.6.1.X<br />

Celgene Corporation<br />

271

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