Literature DB >> 16349018

Estimating the growth rate of slowly growing marine bacteria from RNA content.

P F Kemp1, S Lee, J Laroche.   

Abstract

In past studies of enteric bacteria such as Escherichia coli, various measures of cellular RNA content have been shown to be strongly correlated with growth rate. We examined this correlation for four marine bacterial isolates. Isolates were grown in chemostats at four or five dilution rates, yielding growth rates that spanned the range typically determined for marine bacterial communities in nature (mu = 0.01 to 0.25 h). All measures of RNA content (RNA cell, RNA:biovolume ratio, RNA:DNA ratio, RNA:DNA:biovolume ratio) were significantly different among isolates. Normalizing RNA content to cell volume substantially reduced, but did not eliminate, these differences. On average, the correlation between mu and the RNA:DNA ratio accounted for 94% of variance when isolates were considered individually. For data pooled across isolates (analogous to an average measurement for a community), the ratio of RNA:DNA mum (cell volume) accounted for nearly half of variance in mu (r = 0.47). The maximum RNA:DNA ratio for each isolate was extrapolated from regressions. The regression of (RNA:DNA)/(RNA:DNA)(max) on mu was highly significant (r = 0.76 for data pooled across four isolates) and virtually identical for three of the four isolates, perhaps reflecting an underlying common relationship between RNA content and growth rate. The dissimilar isolate was the only one derived from sediment. Cellular RNA content is likely to be a useful predictor of growth rate for slowly growing marine bacteria but in practice may be most successful when applied at the level of individual species.

Entities:  

Year:  1993        PMID: 16349018      PMCID: PMC182325          DOI: 10.1128/aem.59.8.2594-2601.1993

Source DB:  PubMed          Journal:  Appl Environ Microbiol        ISSN: 0099-2240            Impact factor:   4.792


  12 in total

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6.  Role of ribosome degradation in the death of starved Escherichia coli cells.

Authors:  B D Davis; S M Luger; P C Tai
Journal:  J Bacteriol       Date:  1986-05       Impact factor: 3.490

7.  DNA hybridization to compare species compositions of natural bacterioplankton assemblages.

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Authors:  E F DeLong; G S Wickham; N R Pace
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Authors:  A L Koch
Journal:  Adv Microb Physiol       Date:  1971       Impact factor: 3.517

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  73 in total

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Journal:  Appl Environ Microbiol       Date:  2000-05       Impact factor: 4.792

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Authors:  A Pernthaler; J Pernthaler; H Eilers; R Amann
Journal:  Appl Environ Microbiol       Date:  2001-09       Impact factor: 4.792

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4.  Estimation of bacterial cell numbers in humic acid-rich salt marsh sediments with probes directed to 16S ribosomal DNA

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5.  Detection and characterization of a dehalogenating microorganism by terminal restriction fragment length polymorphism fingerprinting of 16S rRNA in a sulfidogenic, 2-bromophenol-utilizing enrichment.

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Journal:  J Geophys Res       Date:  2006-11-07

8.  Growth rate regulation of rRNA content of a marine synechococcus (Cyanobacterium) strain

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9.  In situ activity of suspended and immobilized microbial communities as measured by fluorescence lifetime imaging.

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10.  Flow cytometric analysis of activated sludge with rRNA-targeted probes.

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Journal:  Appl Environ Microbiol       Date:  1995-05       Impact factor: 4.792

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