MOLECULAR-CLONING AND SEQUENCE-ANALYSIS OF 2 ENDOINULINASE GENES FROMASPERGILLUS-NIGER

Citation
K. Ohta et al., MOLECULAR-CLONING AND SEQUENCE-ANALYSIS OF 2 ENDOINULINASE GENES FROMASPERGILLUS-NIGER, Bioscience, biotechnology, and biochemistry, 62(9), 1998, pp. 1731-1738
Citations number
28
Categorie Soggetti
Biology,Agriculture,"Biothechnology & Applied Migrobiology","Food Science & Tenology
ISSN journal
09168451
Volume
62
Issue
9
Year of publication
1998
Pages
1731 - 1738
Database
ISI
SICI code
0916-8451(1998)62:9<1731:MASO2E>2.0.ZU;2-B
Abstract
Two genomic DNAs encoding endoinulinase from Aspergillus niger 12 were cloned and sequenced. Open reading frames (ORFs) of the endoinulinase genes, inuA and inuB, both consisted of 1,548 nucleotides encoding 51 6 amino acids. It was suggested that the coding regions were not inter rupted by introns, The ORFs differed from each other by 23 nucleotide substitutions or by eight amino acid replacements, indicating that the inuA and inuB genes arose by gene duplication. Each mature enzyme of 493 amino acids was preceded by a hydrophobic signal peptide of 23 ami no acids. The enzymes contained two Cys residues and Eve potential sit es for N-linked glycosylation. Partial amino acid sequences of the sec reted enzyme suggested that it originated from the inuB gene product. The deduced amino acid sequences of the mature A. niger enzymes showed 73% identity with that of the Penicillium purpurogenum endoinulinase.