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Applied and Environmental Microbiology, November 2005, p. 6776-6783, Vol. 71, No. 11
0099-2240/05/$08.00+0     doi:10.1128/AEM.71.11.6776-6783.2005
Copyright © 2005, American Society for Microbiology. All Rights Reserved.

Effect of Different Carbon Sources on Community Composition of Bacterial Enrichments from Soil

Boris Wawrik,^1* Lee Kerkhof,² Jerome Kukor,^1,3 and Gerben Zylstra^1,4

Biotechnology Center for Agriculture and the Environment,¹ Institute of Marine and Coastal Sciences,² Department of Environmental Sciences,³ Department of Biochemistry and Microbiology, Cook College, Rutgers University New Brunswick, New Jersey⁴

Received 10 January 2005/ Accepted 22 June 2005

Soil is a highly heterogeneous matrix, which can contain thousands of different bacterial species per gram. Only a small component of this diversity (maybe <1%) is commonly captured using standard isolation techniques, although indications are that a larger proportion of the soil community is in fact culturable. Better isolation techniques yielding greater bacterial diversity would be of benefit for understanding the metabolic activity and capability of many soil microorganisms. We studied the response of soil bacterial communities to carbon source enrichment in small matrices by means of terminal restriction fragment length polymorphism (TRFLP) analysis. The community composition of replicate enrichments from soil displayed high variability, likely attributable to soil heterogeneity. An analysis of TRFLP data indicated that enrichment on structurally similar carbon sources selected for similar bacterial communities. The same analysis indicated that communities first enriched on glucose or benzoate and subsequently transferred into medium containing an alternate carbon source retained a distinct community signature induced by the carbon source used in the primary enrichment. Enrichment on leucine presented a selective challenge that was able to override the imprint left by primary enrichment on acetate. In a time series experiment community change was most rapid 18 hours after inoculation, corresponding to exponential growth. Community composition did not stabilize even 4 days after secondary enrichment. Four different soil types were enriched on four different carbon sources. TRFLP analysis indicated that in three out of four cases communities enriched on the same carbon source were more similar regardless of which soil type was used. Conversely, the garden soil samples yielded similar enrichment communities regardless of the enrichment carbon source. Our results indicate that in order to maximize the diversity of bacteria recovered from the environment, multiple enrichments should be performed using a chemically diverse set of carbon sources.

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* Corresponding author. Mailing address: Rutgers University, New Brunswick, NJ 08901-8521. Phone: (732) 932-8165. Fax: (732) 932-6535. E-mail: wawrik{at}aesop.rutgers.edu.

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Applied and Environmental Microbiology, November 2005, p. 6776-6783, Vol. 71, No. 11
0099-2240/05/$08.00+0     doi:10.1128/AEM.71.11.6776-6783.2005
Copyright © 2005, American Society for Microbiology. All Rights Reserved.

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