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Cellulose synthase activity in membrane preparations of A.
xylinum was determined according to the procedure of Lin and Brown (13). For
enzyme assays, approximately 150 mg of membrane protein was incubated at
308C for 30 min in a reaction mixture with a final concentration of 20 mM
UDP-[14C]glucose and 20 mM cyclic diguanylic acid (c-di-GMP) (gift from J. H.
van Boom, Department of Organic Chemistry, Leiden, The Netherlands), and
the radioactivity present in the alkali-insoluble product obtained after boiling
was used to determine the cellulose synthase activity. Protein concentrations
were determined by Peterson¡¯s modification of the micro-Lowry method (19)
with a protein assay kit (Sigma).

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Identification of a second cellulose synthase gene (acsAII) in Acetobacter xylinum
J. Bacteriol. 1995, 177(18):5276.

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13 Lin, F. C., and R. M. Brown, Jr. 1989. Purification of cellulose synthase from
Acetobacter xylinum, p. 473¨C492. In C. Schuerch (ed.), Cellulose and wood¡ª
chemistry and technology. John Wiley and Sons, New York.
19 Peterson, G. L. 1977. A simplification of the protein assay method of Lowry
et al. which is more generally applicable. Anal. Biochem. 83:346¨C356.

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Cellulose synthase activity in membrane preparations of A.
xylinum was determined according to the procedure of Lin and Brown (13). For
enzyme assays,  ...

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