O. Salazar et al., Cloning and expression of an Oerskovia xanthineolytica beta-1,3-glucanase in Escherichia coli, BIOTECH LET, 21(9), 1999, pp. 797-802
An Escherichia coli recombinant system produced a soluble beta-1,3-glucanas
e (BglII) cloned from Oerskovia xanthineolytica. The protein was obtained i
n a truncated form derived from the complete polypeptide. Cell fractionatio
n studies show that 80% of the glucanase was retained in the periplasmic sp
ace after 20 h of induction. If cells were grown with glycine, 60% of the g
lucanase was released from the periplasm.