The extracellular xylanase from Bacillus stearothermophilus T-6 is a thermo
stable alkaline tolerant enzyme that was found to bleach pulp optimally at
pH 9 and 65 degrees C, and was successfully used in a large-scale biobleach
ing mill trial. In an attempt to obtain a heavy atom derivative suitable fo
r complete X-ray analysis, xylanase T-6 was labeled biosynthetically with s
eleno-methionine, resulting in a 'built-in' array of atoms with specific X-
ray anomalous scattering signal. Optimization of growth conditions resulted
in over 0.8 g of homogenous seleno-methionine xylanase T-6 per liter cultu
re. The seleno-methionine enzyme was shown to be fully active and produced
single crystals suitable for complete multiple wavelength anomalous diffrac
tion (MAD) structural analysis. (C) 2000 Elsevier Science B.V. All rights r
eserved.