Nucleotide Sequence of the -Amylase-Pullulanase Gene from Clostridium Thermohydrosulfuricum
- 1 March 1990
- journal article
- research article
- Published by Microbiology Society in Journal of General Microbiology
- Vol. 136 (3) , 447-454
- https://doi.org/10.1099/00221287-136-3-447
Abstract
The nucleotide sequence of the gene (apu) encoding the thermostable .alpha.-amylase-pullulanase of Clostridium thermohydrosulfuricum was determined. An open reading frame of 4425 bp was present. The deduced polypeptide (Mr 165600), including a 31 amino acid putative signal sequence, comprised 1475 amino acids, with no cysteine residues. The structural gene was preceded by the consensus promoter sequence TTGACA TATAAT, a putative regulatory sequence and a putative ribosome-binding sequence AAAGGGGG. The codon usage resembled that of Bacillus genes. The deduced sequence of the mature apu product showed similarities to various amylolytic enzymes, especially the neopullulanase of Bacillus stearothermophilus, whereas the signal sequence showed similarity to those of the .alpha.-amylases of B. stearothermophilus and B. subtilis. Three regions thought to be highly conserved in the primary structure of .alpha.-amylases could also be distinguished in the apu product, two being partly ''duplicated'' in this .alpha.-1,4/.alpha.-1,4-active enzyme.Keywords
This publication has 25 references indexed in Scilit:
- Molecular cloning, DNA nucleotide sequencing, and expression in Bacillus subtilis cells of the Bacillus macerans cyclodextrin glucanotransferase geneJournal of Bacteriology, 1986
- Regulation and genetic enhancement of glucoamylase and pullulanase production in Clostridium thermohydrosulfuricumJournal of Bacteriology, 1985
- Complete Nucleotide Sequence of a Gene Coding for Heat- and pH-Stable α-Amylase of Bacillus licheniformis: Comparison of the Amino Acid Sequences of Three Bacterial Liquefying α-Amylases Deduced from the DNA Sequences1The Journal of Biochemistry, 1985
- Two barley alpha-amylase gene families are regulated differently in aleurone cells.Journal of Biological Chemistry, 1985
- Improved M13 phage cloning vectors and host strains: nucleotide sequences of the M13mpl8 and pUC19 vectorsGene, 1985
- Structure and Possible Catalytic Residues of Taka-Amylase AThe Journal of Biochemistry, 1984
- Preferential codon usage in prokaryotic genes: the optimal codon-anticodon interaction energy and the selective codon usage in efficiently expressed genesGene, 1982
- A simple method for displaying the hydropathic character of a proteinJournal of Molecular Biology, 1982
- Isolation from soil and properties of the extreme thermophile Clostridium thermohydrosulfuricumJournal of Bacteriology, 1979
- DNA sequencing with chain-terminating inhibitorsProceedings of the National Academy of Sciences, 1977