Providing sufficient biocatalyst to support the demands of multi tonne prod
uct supply can be problematical. Here we describe how screening for and clo
ning a gamma-lactamase overcame biocatalyst supply issues, and greatly impr
oved the actual biocatalytic process. The isolation of an expressing gamma-
lactamase clone from a gene library necessitated a combination of classical
molecular biology techniques together with innovative screening methods to
identify a functional clone. Once isolated the enzyme was characterised wi
th regard to its process performance and proved to be active at 500 g L-1 s
ubstrate. Further development of the recombinant fermentation and downstrea
m processing has resulted in the ability to produce sufficient biocatalyst
from one 5001 fermentation to resolve 5 metric tonnes of (+/-)-lactam, whil
st simplifying the process chemistry greatly. (C) 1999 Elsevier Science Ltd
. All rights reserved.