AEM
Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Zhong, Z.
Right arrow Articles by Caspi, R.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Zhong, Z.
Right arrow Articles by Caspi, R.
Agricola
Right arrow Articles by Zhong, Z.
Right arrow Articles by Caspi, R.

 Previous Article  |  Next Article 

Applied and Environmental Microbiology, December 2001, p. 5771-5779, Vol. 67, No. 12
0099-2240/01/$04.00+0   DOI: 10.1128/AEM.67.12.5771-5779.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.

Sequence Analysis of a 101-Kilobase Plasmid Required for Agar Degradation by a Microscilla Isolate

Zhenping Zhong,1 Aresa Toukdarian,1,* Donald Helinski,1 Vic Knauf,2,§ Sean Sykes,3 Jane E. Wilkinson,3 Colleen O'Bryne,3 Terry Shea,3 Craig DeLoughery,3,dagger and Ron Caspi1,Dagger

Division of Biology and Center for Molecular Genetics, University of California, San Diego, La Jolla, California 92093-03221; Calgene, Inc., Davis, California 956162; and Cereon Genomics, Cambridge, Massachusetts 021393

Received 23 May 2001/Accepted 4 September 2001

An agar-degrading marine bacterium identified as a Microscilla species was isolated from coastal California marine sediment. This organism harbored a single 101-kb circular DNA plasmid designated pSD15. The complete nucleotide sequence of pSD15 was obtained, and sequence analysis indicated a number of genes putatively encoding a variety of enzymes involved in polysaccharide utilization. The most striking feature was the occurrence of five putative agarase genes. Loss of the plasmid, which occurred at a surprisingly high frequency, was associated with loss of agarase activity, supporting the sequence analysis results.


* Corresponding author. Mailing address: Division of Biology and Center for Molecular Genetics, University of California, San Diego, 9500 Gilman Dr., La Jolla, CA 92093-0322. Phone: (858) 534-2460. Fax: (858) 534-0559. E-mail: atoukdar{at}ucsd.edu.

dagger Present address: Aventis, Cambridge, MA 02139.

Dagger Present address: Pangene Corporation, Fremont, CA 94538.

§ Present address: Tilligen, Inc., Seattle, WA 98101.


Applied and Environmental Microbiology, December 2001, p. 5771-5779, Vol. 67, No. 12
0099-2240/01/$04.00+0   DOI: 10.1128/AEM.67.12.5771-5779.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.



This article has been cited by other articles:




Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
J. Bacteriol. Microbiol. Mol. Biol. Rev. Eukaryot. Cell All ASM Journals

Copyright © 2001 by the American Society for Microbiology. All rights reserved.