Extracellular enzyme synthesis in a sporulation-deficient strain of Bacillus licheniformis

A. B. Fleming, M. Tangney, P. L. Jorgensen, B. Diderichsen, F. G. Priest

    Research output: Contribution to journalArticle

    Abstract

    A deletion of the spoIIAC gene of Bacillus licheniformis was prepared in vitro by using the splicing-by-overlap-extension technique. This gene was introduced into B. licheniformis on a temperature-sensitive plasmid, and following integration and excision from the chromosome, a precisely located deletion on the chromosomal gene was prepared. The mutated bacterium was totally asporogenous and formed abortively disporic cells characterized by asymmetric septa at the poles of the cells. Qualitative plate tests revealed that the bacterium synthesized normal levels of DNase, polygalacturonate lyase, protease, RNase, and xylanase, but the hydrolysis zones due to ß- 1,3-glucanase and carboxymethyl cellulase activity were smaller in the mutant than in the parent strain. The synthesis of alkaline protease was the same in batch cultures of the mutant and the parent during prolonged incubation for 72 h, but the a-amylase yields were reduced by about 30% by the mutation.

    Original languageEnglish
    Pages (from-to)3775-3780
    Number of pages6
    JournalApplied and Environmental Microbiology
    Volume61
    Issue number11
    Publication statusPublished - 1995

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    Fleming, A. B., Tangney, M., Jorgensen, P. L., Diderichsen, B., & Priest, F. G. (1995). Extracellular enzyme synthesis in a sporulation-deficient strain of Bacillus licheniformis. Applied and Environmental Microbiology, 61(11), 3775-3780.