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Journal of Bacteriology, August 2006, p. 5551-5560, Vol. 188, No. 15
0021-9193/06/$08.00+0     doi:10.1128/JB.00236-06
Copyright © 2006, American Society for Microbiology. All Rights Reserved.

Identification and Characterization of an Azotobacter vinelandii Type I Secretion System Responsible for Export of the AlgE-Type Mannuronan C-5-Epimerases

Martin Gimmestad,¹ Magnus Steigedal,¹ Helga Ertesvåg,¹ Soledad Moreno,² Bjørn Erik Christensen,¹ Guadalupe Espín,² and Svein Valla^1*

Department of Biotechnology, NTNU Norwegian University of Science and Technology, N-7491 Trondheim, Norway,¹ Departamento de Microbiología Molecular, Instituto de Biotecnología, Universidad Nacional Autónoma de México, Cuernavaca, Morelos, Mexico²

Received 15 February 2006/ Accepted 25 May 2006

Alginate is a linear copolymer of ß-D-mannuronic acid and its C-5-epimer, -L-guluronic acid. During biosynthesis, the polymer is first made as mannuronan, and various fractions of the monomers are then epimerized to guluronic acid by mannuronan C-5-epimerases. The Azotobacter vinelandii genome encodes a family of seven extracellular such epimerases (AlgE1 to AlgE7) which display motifs characteristic for proteins secreted via a type I pathway. Putative ATPase-binding cassette regions from the genome draft sequence of the A. vinelandii OP strain and experimentally verified type I transporters from other species were compared. This analysis led to the identification of one putative A. vinelandii type I system (eexDEF). The corresponding genes were individually disrupted in A. vinelandii strain E, and Western blot analysis using polyclonal antibodies against all AlgE epimerases showed that these proteins were present in wild-type culture supernatants but absent from the eex mutant supernatants. Consistent with this, the wild-type strain and the eex mutants produced alginate with about 20% guluronic acid and almost pure mannuronan (2% guluronic acid), respectively. The A. vinelandii wild type is able to enter a particular desiccation-tolerant resting stage designated cyst. At this stage, the cells are surrounded by a rigid coat in which alginate is a major constituent. Such a coat was formed by wild-type cells in a particular growth medium but was missing in the eex mutants. These mutants were also found to be unable to survive desiccation. The reason for this is probably that continuous stretches of guluronic acid residues are needed for alginate gel formation to take place.

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* Corresponding author. Mailing address: Department of Biotechnology, NTNU Norwegian University of Science and Technology, N-7491 Trondheim, Norway. Phone: (47)73593320. Fax: (47)73591283. E-mail: svein.valla{at}biotech.ntnu.no.

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Journal of Bacteriology, August 2006, p. 5551-5560, Vol. 188, No. 15
0021-9193/06/$08.00+0     doi:10.1128/JB.00236-06
Copyright © 2006, American Society for Microbiology. All Rights Reserved.

This article has been cited by other articles:

• Gimmestad, M., Ertesvag, H., Heggeset, T. M. B., Aarstad, O., Svanem, B. I. G., Valla, S. (2009). Characterization of Three New Azotobacter vinelandii Alginate Lyases, One of Which Is Involved in Cyst Germination. J. Bacteriol. 191: 4845-4853 [Abstract] [Full Text]