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PMID: 1555601 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Cloning and expression of an Arabidopsis nitrilase which can convert indole-3-acetonitrile to the plant hormone, indole-3-acetic acid.

European journal of biochemistry ·Vol. 205 ·No. 1 ·1992-04-01 ·Pages 417-24

Bartling D, Seedorf M, Mithöfer A, Weiler EW

Abstract

From an Arabidopsis thaliana cDNA expression library, a cDNA clone was isolated, characterized and sequenced which, at the amino acid level, resembled the Klebsiella ozaenae bromoxynil nitrilase encoded by the bxn gene. The cDNA contained a long open reading frame, starting from two possible neighbouring ATG codons and capable of encoding 340 or 346 amino acids with calculated molecular masses of 37526 Da or 38176 Da, respectively. The sequence similarity between the deduced polypeptides from the Arabidopsis cDNA and bxn was clustered in three domains, one at the C-terminus, one in the center and one near the N-terminus of the two proteins, suggesting important functional elements in these parts of the proteins. The cDNA was cloned into different vectors under the control of the lacZ promotor and was functionally expressed by induction with isopropyl-beta-D-thiogalactoside. Using a combination of high-performance liquid chromatography, monoclonal-antibody based enzyme-linked immunosorbent assay and mass spectroscopy, it was shown that the isolated cDNA clone encodes an enzymatically active nitrilase which is able to convert indole-3-acetonitrile to the plant growth hormone, indole-3-acetic-acid.

MeSH Terms
Amino Acid Sequence Aminohydrolases/genetics,metabolism Base Sequence Blotting, Southern Cloning, Molecular DNA/genetics Gene Expression Indoleacetic Acids/metabolism Indoles/antagonists & inhibitors,metabolism Molecular Sequence Data Plant Growth Regulators/metabolism Plants/enzymology Restriction Mapping Sequence Homology, Nucleic Acid
Chemicals
Indoleacetic Acids Indoles Plant Growth Regulators indoleacetic acid DNA indole-3-acetonitrile Aminohydrolases nitrilase
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Bartling D
Lehrstuhl für Pflanzenphysiologie, Ruhr-Universität, Bochum, Federal Republic of Germany.
Seedorf M
Mithöfer A
Weiler E W
Article Info
Journal
European journal of biochemistry
Abbr.
Eur J Biochem
ISSN
0014-2956
Published
1992-04-01
Pages
417-24
Language
English
Region
England
NLM ID
0107600
Subset
IM
Databases
GENBANK
S87180, S87218, S87221, S87223, X63445, X63577, X65178, X65179, X65180, X65181
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