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Journal of Bacteriology, December 2002, p. 6681-6689, Vol. 184, No. 23
0021-9193/02/$04.00+0 DOI: 10.1128/JB.184.23.6681-6689.2002
Copyright © 2002, American Society for Microbiology. All Rights Reserved.
A Sinorhizobium meliloti Lipopolysaccharide Mutant Altered in Cell Surface Sulfation
David H. Keating,1* Michael G. Willits,2,
and Sharon R. Long1,2
Howard Hughes Medical Institute,1
Department of Biology, Stanford University, Stanford, California 943052
Received 27 September 2001/
Accepted 9 August 2002
The Rhizobium-legume symbiosis involves the formation of a novel plant organ, the nodule, in which intracellular bacteria reduce molecular dinitrogen in exchange for plant photosynthates. Nodule development requires a bacterial signal referred to as Nod factor, which in Sinorhizobium meliloti is a ß-(1,4)-linked tetramer of N-acetylglucosamine containing N-acyl and O-acetyl modifications at the nonreducing end and a critical 6-O-sulfate at the reducing end. This sulfate modification requires the action of three gene products: nodH, which catalyzes the sulfonyl transfer, and nodPQ, which produce the activated form of sulfate, 3'-phosphoadenosine-5'-phosphosulfate. It was previously reported that S. meliloti cell surface polysaccharides are also covalently modified by sulfate in a reaction dependent on NodPQ. We have further characterized this unique form of bacterial carbohydrate modification. Our studies have determined that one of the nodPQ mutant strains used in the initial study of sulfation of cell surface harbored a second unlinked mutation. We cloned the gene affected by this mutation (referred to as lps-212) and found it to be an allele of lpsL, a gene previously predicted to encode a UDP-glucuronic acid epimerase. We demonstrated that lpsL encoded a UDP-glucuronic acid epimerase activity that was reduced in the lps-212 mutant. The lps-212 mutation resulted in an altered lipopolysaccharide structure that was reduced in sulfate modification in vitro and in vivo. Finally, we determined that the lps-212 mutation resulted in a reduced ability to elicit the formation of plant nodules and by altered infection thread structures that aborted prematurely.
* Corresponding author. Present address: Department of Microbiology and Immunology, Building 105, Loyola University Chicago, 2160 South First Avenue, Maywood, IL 60153. Phone: (708) 216-9472. Fax: (708) 216-9574.
Present address: Novartis Crop Protection, Inc., Biotechnology and Genomics Center, Research Triangle Park, NC 27709-2257.
Journal of Bacteriology, December 2002, p. 6681-6689, Vol. 184, No. 23
0021-9193/02/$04.00+0 DOI: 10.1128/JB.184.23.6681-6689.2002
Copyright © 2002, American Society for Microbiology. All Rights Reserved.
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