Literature DB >> 2391488

Nucleotide sequence of the alpha-amylase-pullulanase gene from Clostridium thermohydrosulfuricum.

H Melasniemi1, M Paloheimo, L Hemiö.   

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 165,600), 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-1,6-active enzyme.

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Year:  1990        PMID: 2391488     DOI: 10.1099/00221287-136-3-447

Source DB:  PubMed          Journal:  J Gen Microbiol        ISSN: 0022-1287


  19 in total

1.  Proposed acquisition of an animal protein domain by bacteria.

Authors:  P Bork; R F Doolittle
Journal:  Proc Natl Acad Sci U S A       Date:  1992-10-01       Impact factor: 11.205

2.  Effect of C-terminal truncation on enzyme properties of recombinant amylopullulanase from Thermoanaerobacter pseudoethanolicus.

Authors:  Fu-Pang Lin; Yi-Hsuan Ho; Hsu-Yang Lin; Hui-Ju Lin
Journal:  Extremophiles       Date:  2012-03-06       Impact factor: 2.395

3.  Structure of the gene encoding cyclomaltodextrinase from Clostridium thermohydrosulfuricum 39E and characterization of the enzyme purified from Escherichia coli.

Authors:  S M Podkovyrov; J G Zeikus
Journal:  J Bacteriol       Date:  1992-08       Impact factor: 3.490

4.  Comparison of the domain-level organization of starch hydrolases and related enzymes.

Authors:  H M Jespersen; E A MacGregor; M R Sierks; B Svensson
Journal:  Biochem J       Date:  1991-11-15       Impact factor: 3.857

5.  Analysis of the active center of Bacillus stearothermophilus neopullulanase.

Authors:  T Kuriki; H Takata; S Okada; T Imanaka
Journal:  J Bacteriol       Date:  1991-10       Impact factor: 3.490

6.  Biochemical characterization of engineered amylopullulanase from Thermoanaerobacter ethanolicus 39E-implicating the non-necessity of its 100 C-terminal amino acid residues.

Authors:  Hsu-Yang Lin; Hsu-Han Chuang; Fu-Pang Lin
Journal:  Extremophiles       Date:  2008-05-24       Impact factor: 2.395

7.  Tracing the spread of fibronectin type III domains in bacterial glycohydrolases.

Authors:  E Little; P Bork; R F Doolittle
Journal:  J Mol Evol       Date:  1994-12       Impact factor: 2.395

8.  Characterization of chitinase C from a marine bacterium, Alteromonas sp. strain O-7, and its corresponding gene and domain structure.

Authors:  H Tsujibo; H Orikoshi; K Shiotani; M Hayashi; J Umeda; K Miyamoto; C Imada; Y Okami; Y Inamori
Journal:  Appl Environ Microbiol       Date:  1998-02       Impact factor: 4.792

9.  Regional sequence homologies in starch-degrading enzymes.

Authors:  B J Janse; A J Steyn; I S Pretorius
Journal:  Curr Genet       Date:  1993-11       Impact factor: 3.886

10.  Pullulanase of Thermoanaerobacterium thermosulfurigenes EM1 (Clostridium thermosulfurogenes): molecular analysis of the gene, composite structure of the enzyme, and a common model for its attachment to the cell surface.

Authors:  M Matuschek; G Burchhardt; K Sahm; H Bahl
Journal:  J Bacteriol       Date:  1994-06       Impact factor: 3.490

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