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Analysis of the microbial functional diversity within water-stressed soil communities by flow cytometric analysis and CTC+ cell sorting. / Whiteley, Andrew S; Griffiths, Robert I; Bailey, Mark J.
Yn: Journal of Microbiological Methods, Cyfrol 54, Rhif 2, 08.2003, t. 257-267.

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Whiteley AS, Griffiths RI, Bailey MJ. Analysis of the microbial functional diversity within water-stressed soil communities by flow cytometric analysis and CTC+ cell sorting. Journal of Microbiological Methods. 2003 Awst;54(2):257-267. doi: 10.1016/S0167-7012

Author

Whiteley, Andrew S ; Griffiths, Robert I ; Bailey, Mark J. / Analysis of the microbial functional diversity within water-stressed soil communities by flow cytometric analysis and CTC+ cell sorting. Yn: Journal of Microbiological Methods. 2003 ; Cyfrol 54, Rhif 2. tt. 257-267.

RIS

TY - JOUR

T1 - Analysis of the microbial functional diversity within water-stressed soil communities by flow cytometric analysis and CTC+ cell sorting

AU - Whiteley, Andrew S

AU - Griffiths, Robert I

AU - Bailey, Mark J

PY - 2003/8

Y1 - 2003/8

N2 - Total and active cell counts within soil samples were determined by culture-independent methods using flow cytometry and preparative Nycodenz gradient centrifugation. Whole cells were purified from soil cores and total extractable cell counts assessed by SYBR Green II fluorescence, while active cell counts were determined by 5-cyano-2,3-ditolyl tetrazolium chloride reduction (CTC+ cells). Parallel microcosms, maintained at either field water capacity or subjected to drying, indicated that the total extractable cell count remained between 108 and 109 g−1 (dry weight). In contrast, the CTC+ active count fell threefold in dried microcosms (6% of total cell count) when compared to wetted microcosms (18% of total cell count). Specifically, these data highlighted an overall deactivation of microbial biomass during water stress, with 16S rDNA analyses of flow-sorted CTC+ cells demonstrating shifts within the active diversity. Flow cytometry coupled with cell purification techniques represents a significant tool for operationally defining an active and redundant microbial component within soil communities and is demonstrated during water stress.

AB - Total and active cell counts within soil samples were determined by culture-independent methods using flow cytometry and preparative Nycodenz gradient centrifugation. Whole cells were purified from soil cores and total extractable cell counts assessed by SYBR Green II fluorescence, while active cell counts were determined by 5-cyano-2,3-ditolyl tetrazolium chloride reduction (CTC+ cells). Parallel microcosms, maintained at either field water capacity or subjected to drying, indicated that the total extractable cell count remained between 108 and 109 g−1 (dry weight). In contrast, the CTC+ active count fell threefold in dried microcosms (6% of total cell count) when compared to wetted microcosms (18% of total cell count). Specifically, these data highlighted an overall deactivation of microbial biomass during water stress, with 16S rDNA analyses of flow-sorted CTC+ cells demonstrating shifts within the active diversity. Flow cytometry coupled with cell purification techniques represents a significant tool for operationally defining an active and redundant microbial component within soil communities and is demonstrated during water stress.

KW - Flow cytometry

KW - 5-cyano-2,3-ditolyl tetrazolium chloride

KW - CTC

KW - Soil microbes

U2 - 10.1016/S0167-7012

DO - 10.1016/S0167-7012

M3 - Article

VL - 54

SP - 257

EP - 267

JO - Journal of Microbiological Methods

JF - Journal of Microbiological Methods

SN - 0167-7012

IS - 2

ER -