Rational design and PCR-based synthesis of an artificial Schizophyllum commune xylanase gene.

Abstract:

:A synthetic gene encoding the Schizophyllum commune xylanase XynA was constructed by a novel PCR-based procedure. Three long oligonucleotides were synthesized and used in combination with flanking PCR primers to generate a 607 base pair gene which contained 31 unique locations for restriction enzyme cleavage. The amino acid sequence was tailored for expression in Escherichia coli by using only those codons found in highly expressed E. coli genes. The availability of the gene will facilitate analysis of the structure and function of this and other beta-(1,4) xylanases.

journal_name

Nucleic Acids Res

journal_title

Nucleic acids research

authors

Graham RW,Atkinson T,Kilburn DG,Miller RC Jr,Warren RA

doi

10.1093/nar/21.21.4923

subject

Has Abstract

pub_date

1993-10-25 00:00:00

pages

4923-8

issue

21

eissn

0305-1048

issn

1362-4962

journal_volume

21

pub_type

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