Bm. Long et al., Cellular microcystin content in N-limited Microcystis aeruginosa can be predicted from growth rate, APPL ENVIR, 67(1), 2001, pp. 278-283
Cell quotas of microcystin (Q(MCYST); femtomoles of MCYST per cell), protei
n, and chlorophyll a (Chl a), cell dry weight, and cell volume were measure
d over a range of growth rates in N-limited chemostat cultures of the toxic
cyanobacterium Microcystis aeruginosa MASH 01-A19. There was a positive li
near relationship between Q(MCYST) and specific growth rate (mu), from whic
h we propose a generalized model that enables Q(MCYST) at any nutrient-limi
ted growth rate to be predicted based on a single batch culture experiment,
The model predicts Q(MCYST) from mu, mu (max) (maximum specific growth rat
e), Q(MCYST) (maximum cell quota), and Q(MCYST) (minimum cell quota). Under
the conditions examined in this study, we predict a Q(MCYST) of 0.129 fmol
cell(-1) at mu (max) and a Q(MCYST) of 0.050 fmol cell(-1) at mu = 0, Net
MCYST production rate (R-MCYST) asymptotes to zero at mu = 0 and reaches a
maximum of 0.155 fmol cell(-1) day(-1) at mu (max). MCYST/dry weight ratio
(milligrams per gram [dry weight]) increased linearly with mu, whereas the
MCYST/protein ratio reached a maximum at intermediate mu. In contrast, the
MCYST/Chl a ratio remained constant. Cell volume correlated negatively with
mu, leading to an increase in intracellular MCYST concentration at high IJ
Taken together, our results show that fast-growing cells of N-limited M. a
eruginosa are smaller, are of lower mass, and have a higher intracellular M
CYST quota and concentration than slow-growing cells, The data also highlig
ht the importance of determining cell MCYST quotas, as potentially confusin
g interpretations can arise from determining MCYST content as a ratio to ot
her cell components.