Streptomyces coelicolor "Müller" DSM3030 excretes a lysozyme comprising both beta-1,4-N-acetyl- and beta-1,4-N,6-O-diacetyl muramidase activities. The lysozyme is named Cellosyl. Gene libraries have been established using genomic DNA from the wild-type strain, S. coelicolor DSM3030, and from an overproducing mutant, S. coelicolor HP1, which exhibits about a twofold increase in lysozyme production. The lysozyme-encoding genes (cel) from both strains were detected by oligodeoxynucleotide hybridization. The nucleotide sequence of the cel genes isolated from both strains was shown to be identical. The different levels of lysozyme production could not be correlated with any mutations at the cel gene locus. The cel gene isolated from the wild-type strain could not be expressed in some other species of Streptomyces. However, self-cloning of the cel gene into S. coelicolor DSM3030 and HP1 resulted in a 2.5-fold increase in lysozyme production.
SynopsisLow molecular weight /j, 1 + 4-glucans (cellodextrins) are favorably prepared by cleavage of cellulose in liquid hydrogen fluoride at temperatures between -15 and -30° C. This is due to the suppression of the reversion reaction in that low temperature range. Under conditions favorable for reversion the presence of water leads to a competing hydrolysis and lowers the average degree of polycondensation. For the preparation of defined 0-glycosides from glucose and alcohols, hydrogen fluoride is not'suitable as a reaction medium. Under reversion conditions, monohydroxy compounds are inferior in their reactivity to the competing carbohydrate molecules, and polyols like sorbitol furnish mixtures of isomeric glycosides. Gaseous hydrogen fluoride represents a highly suitable agent for the degradation of carbohydrate and lignin containing biomass, such as waste wood, for the purpose of providing fermentation raw material. As a model, lignocellulose was studied and the heat of reaction of the hydrogen fluoride sorption and desorption processes were examined. The practically important desorption value was found to be approximately 870 kJ/kg HF:
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