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Applied and Environmental Microbiology, June 1999, p. 2513-2519, Vol. 65, No. 6
Biocontrol of Plant Diseases
Laboratory1 and Soil Microbial Systems
Laboratory,2 USDA Agricultural Research
Service, Beltsville, Maryland, and Department of Plant
Pathology, Rutgers University, New Brunswick, New
Jersey3
Received 4 December 1998/Accepted 19 March 1999
Enterobacter cloacae A-11 is a transposon mutant of
strain 501R3 that was deficient in cucumber spermosphere colonization and in the utilization of certain carbohydrates (D. P. Roberts, C. J. Sheets, and J. S. Hartung, Can. J. Microbiol.
38:1128-1134, 1992). In vitro growth of strain A-11 was reduced or
deficient on most carbohydrates that supported growth of strain 501R3
but was unaffected on fructose, glycerol, and all amino acids and organic acids tested. Colonization by strain A-11 was significantly reduced (P
0099-2240/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
Role of pfkA and General Carbohydrate
Catabolism in Seed Colonization by Enterobacter
cloacae

0.05) for cucumber and radish seeds
compared to that of strain 501R3, but colonization of pea, soybean,
sunflower, and sweet corn seeds was not reduced. Pea seeds released
several orders of magnitude more total carbohydrates and amino acids
than cucumber and radish seeds and approximately 4,000-fold more
fructose. Fructose was the only carbohydrate detected in the seed
exudates which supported wild-type levels of in vitro growth of strain A-11. Soybean, sunflower, and sweet corn seeds also released
significantly greater amounts of fructose and total carbohydrates and
amino acids than cucumber or radish seeds. The exogenous addition of fructose to cucumber and radish seeds at quantities similar to the
total quantity of carbohydrates released from pea seeds over 96 h
increased the populations of strain A-11 to levels comparable to those
of strain 501R3 in sterile sand. Molecular characterization of strain
A-11 indicated that the mini-Tn5 kanamycin transposon was
inserted in a region of the genome with significant homology to
pfkA, which encodes phosphofructo kinase. A comparison of
strain A-11 with Escherichia coli DF456, a known
pfkA mutant, indicated that the nutritional loss phenotypes
were identical. Furthermore, the pfkA homolog cloned from
E. cloacae 501R3 complemented the nutritional loss
phenotypes of both E. coli DF456 and E. cloacae A-11 and restored colonization by strain A-11 to near wild-type levels.
These genetic and biochemical restoration experiments provide strong
evidence that the quantities of reduced carbon sources found in seed
exudates and the ability of microbes to use these compounds play
important roles in the colonization of the spermosphere.
*
Corresponding author. Mailing address: Biocontrol of
Plant Diseases Laboratory, Bldg. 011A, Rm. 275, 10300 Baltimore Ave., Beltsville, MD 20705. Phone: (301) 504-5680. Fax: (301) 504-5968. E-mail: DROBERTS{at}asrr.arsusda.gov.
Present address: U.S. Patent Office, Arlington, VA 22202.
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