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Molecular and cultural analysis of seasonal actinomycetes in soils from Artemisia tridentata habitat

Gonzalez-Franco AC1, L Robles-Hernandez1, A Nuñez-Barrios1, JL Strap2, DL Crawford3

Facultad de Ciencias Agrotecnológicas, Universidad Autónoma de Chihuahua, Ciudad Universitaria S/N Campus 1, Chihuahua, Chih., 31310, México.
Faculty of Science, University of Ontario Institute of Technology, Oshawa, Ontario, L1H 7K4, Canada
Department of Microbiology, Molecular Biology and Biochemistry, University of Idaho, Moscow, ID 83844-3052, USA.

* Corresponding Author:Address Correspondence to: AC Gonzalez-Franco, e-mail: email; fax 52-614-4391845; Phone 052-614-4391844.

Phyton-International Journal of Experimental Botany 2009, 78(all), 83-90. https://doi.org/10.32604/phyton.2009.78.083

Abstract

In order to understand the temporal dynamics of actinomycete communities of the rhizosphere of the desert plant Artemisia tridentata (sagebrush), two complementary methods were used. They were: (1) 16S rDNA-based PCR coupled with denaturing gradient gel electrophoresis (DGGE), and (2) an agar plate enumeration methodology in which three different media were used to quantify total bacteria, actinomycetes, and fungi. The objective of this research were: (1) to obtain a comprehensive picture of the structure of actinomycete populations, and (2) their dynamics in the rhizosphere of young and old sagebrush plants during two distinct seasons. PCR-DGGE analysis showed that actinomycete groups were less diverse in rhizosphere soils collected in winter than in bulk soils. On the other hand, rhizosphere soil of A. tridentata young plants (RSYP) collected in spring showed an enrichment of actinomycete diversity and/or selection of unique actinomycete populations. This was not the case with the actinomycete populations detected in the rhizosphere soil of old plants (RSOP) in the same season. In this later case, a shift in the dominant bands on PCR-DGGE gels was observed between seasons. Finally, the enumeration analysis showed that actinomycete counts tended to be higher in spring, while total bacteria counts were higher in winter. Although strong soil type effects were detected, more research in the unexplored environment of sagebrush rhizosphere is necessary.

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APA Style
AC, G., Robles-Hernandez, L., Nuñez-Barrios, A., Strap, J., Crawford, D. (2009). Molecular and cultural analysis of seasonal actinomycetes in soils from artemisia tridentata habitat. Phyton-International Journal of Experimental Botany, 78(all), 83-90. https://doi.org/10.32604/phyton.2009.78.083
Vancouver Style
AC G, Robles-Hernandez L, Nuñez-Barrios A, Strap J, Crawford D. Molecular and cultural analysis of seasonal actinomycetes in soils from artemisia tridentata habitat. Phyton-Int J Exp Bot. 2009;78(all):83-90 https://doi.org/10.32604/phyton.2009.78.083
IEEE Style
G. AC, L. Robles-Hernandez, A. Nuñez-Barrios, J. Strap, and D. Crawford "Molecular and cultural analysis of seasonal actinomycetes in soils from Artemisia tridentata habitat," Phyton-Int. J. Exp. Bot., vol. 78, no. all, pp. 83-90. 2009. https://doi.org/10.32604/phyton.2009.78.083

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cc Copyright © 2009 The Author(s). Published by Tech Science Press.
This work is licensed under a Creative Commons Attribution 4.0 International License , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
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