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Applied and Environmental Microbiology, December 2001, p. 5425-5430, Vol. 67, No. 12
Departamento de Ecología,
Genética y Microbiología, Área de
Microbiología, Facultad de Biología, Universidad de
León, León, Spain
Received 26 July 2001/Accepted 14 September 2001
A xylanolytic strain of Brevibacterium
lactofermentum containing the
Streptomyces halstedii His-tagged
xysA gene was generated. The new strain contains DNA
derived from S. halstedii, expresses xylanolytic activity, and was obtained by an integrative process mediated by a conjugative plasmid targeted to a dispensable chromosomal region located downstream from the essential cell division gene ftsZ. The His-tagged Xys1 enzyme was constitutively
expressed under the control of the kan promoter from
Tn5 and was easily purified by use of
Ni-nitrilotriacetic acid-agarose. The new strain is stable for more
than 200 generations, lacks any known antibiotic resistance gene, and
does not need any selective pressure to maintain the integrated gene.
This strategy can be used to integrate any gene into the
B. lactofermentum chromosome and to
maintain it stably without the use of antibiotics for selection.
0099-2240/01/$04.00+0 DOI: 10.1128/AEM.67.12.5425-5430.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
Construction of a Xylanase-Producing Strain of
Brevibacterium lactofermentum by Stable
Integration of an Engineered xysA Gene from
Streptomyces halstedii JM8
*
Corresponding author. Mailing address: Departamento de
Ecología, Genética y Microbiología, Área de
Microbiología, Facultad de Biología, Universidad de
León, 24071 León, Spain. Phone: 34-987-291503. Fax:
34-987-291479. E-mail: degjgs{at}unileon.es.
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