Characterization of the secretion efficiency of a plant signal peptide in Bacillus subtilis
β Scribed by Ribbe, Joachim ;Nagarajan, Vasantha
- Publisher
- Springer
- Year
- 1992
- Tongue
- English
- Weight
- 847 KB
- Volume
- 235
- Category
- Article
- ISSN
- 0026-8925
No coin nor oath required. For personal study only.
β¦ Synopsis
The ability of the Bacillus subtilis secretion machinery to interact with a heterologous signal peptide was studied using a plant (wheat alpha-amylase) signal peptide. The plant signal peptide was capable of mediating secretion of Escherichia coli alkaline phosphatase and B. amyloliquefaciens levansucrase from B. subtilis. This secretion was dependent on the plant signal peptide, as deletion of five amino acids from the hydrophobic core resulted in a block of secretion. Attempts to improve the efficiency of the plant signal peptide in B. subtilis were made by increasing the length of the hydrophobic core from 10 to 16 residues by insertion of 2, 4, 5 or 6 amino acids. None of the alterations improved the secretion efficiency relative to the wild-type plant signal peptide.
π SIMILAR VOLUMES
Barnase, an extracellular RNAse from Bacillus amyloliquefaciens is secreted post-translationally from B. subtilis. The rate of secretion of barnase from B. subtilis was improved by replacement of the barnase signal peptide with a heterologous signal peptide. However, the barnase signal peptide expor
The formation of spores in Bacillus subtrhs is a developmental process under genetic control. The decision to either divide or sporulate is regulated by the state of phosphorylation of the SpoOA transcription factor. Phosphorylated SpoOA (SpoOA -P) is both a repressor and an activator of transcripti
The cellulase gene celA of Clostridium thermocellum coding for the thermostable endoglucanase A was transferred from Escherichia coli to Bacillus subtilis 168 and B. stearothermophilus CU21 using plasmids derived from the Bacillus vector pUB110. When the structural part of the gene was joined to a p
A proximal segment of B.subtilis secY gene was placed under the control of the inducible .spuc. promoter/Lac repressor system. This fusion was integrated into the chromosomal spc operon of B. subtilis via CAMPBELL-like reciprocal recombination. The growth of the resulting strain was strongly IPTG de