Applied and Environmental Microbiology, January 2001, p. 278-283, Vol. 67, No. 1
0099-2240/01/$04.00+0 DOI: 10.1128/AEM.67.1.278-283.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
Department of Botany, La Trobe University, Victoria 3086,1 and CSIRO Land and Water, Indooroopilly, Queensland 4068,2 Australia
Received 25 May 2000/Accepted 11 October 2000
Cell quotas of microcystin (QMCYST;
femtomoles of MCYST per cell), protein, and chlorophyll a
(Chl a), cell dry weight, and cell volume were measured
over a range of growth rates in N-limited chemostat cultures of the
toxic cyanobacterium Microcystis aeruginosa MASH 01-A19.
There was a positive linear relationship between QMCYST and specific growth rate (µ), from
which we propose a generalized model that enables
QMCYST at any nutrient-limited growth rate to
be predicted based on a single batch culture experiment. The model
predicts QMCYST from µ, µmax
(maximum specific growth rate), QMCYSTmax
(maximum cell quota), and QMCYSTmin (minimum
cell quota). Under the conditions examined in this study, we predict a
QMCYSTmax of 0.129 fmol cell
1 at
µmax and a QMCYSTmin of 0.050 fmol cell
1 at µ = 0. Net MCYST production rate
(RMCYST) asymptotes to zero at µ = 0 and
reaches a maximum of 0.155 fmol cell
1 day
1
at µmax. MCYST/dry weight ratio (milligrams per gram
[dry weight]) increased linearly with µ, whereas the MCYST/protein
ratio reached a maximum at intermediate µ. In contrast, the MCYST/Chl
a ratio remained constant. Cell volume correlated
negatively with µ, leading to an increase in intracellular MCYST
concentration at high µ. Taken together, our results show that
fast-growing cells of N-limited M. aeruginosa are smaller,
are of lower mass, and have a higher intracellular MCYST quota and
concentration than slow-growing cells. The data also highlight the
importance of determining cell MCYST quotas, as potentially confusing
interpretations can arise from determining MCYST content as a ratio to
other cell components.
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