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Published on: December 5, 2016
Microcystin aids in cold temperature acclimation: Differences between a toxic Microcystis wildtype and non-toxic
Gwendolyn F Stark1, Robbie M Martin1, Laura E Smith1
1Department of Microbiology, The University of Tennessee, Knoxville, TN, USA.
Lower temperatures increase microcystin production in Microcystis aeruginosa, potentially offering a fitness advantage. A non-toxigenic mutant showed different metabolic responses to cold, suggesting microcystin aids in managing oxidative stress.
Area of Science:
- Environmental microbiology
- Cyanobacterial physiology
- Toxicology
Background:
- Microcystis aeruginosa produces microcystin, a potent toxin.
- Cold temperatures increase microcystin quotas in M. aeruginosa.
- The fitness advantage of microcystin production at lower temperatures is not fully understood.
Purpose of the Study:
- To investigate if increased microcystin production at colder temperatures provides a fitness advantage to M. aeruginosa PCC 7806.
- To compare the physiological and metabolic responses of a wild-type strain to a non-toxigenic mutant under cold stress.
Main Methods:
- Continuous culture growth of M. aeruginosa PCC 7806 and its non-toxigenic mutant (ΔmcyB) at 26°C and 19°C.
- Assessment of cell concentration, cellular physiology, and reactive oxygen species (ROS) damage.
- Transcriptomic analysis to infer metabolic differences.
Main Results:
- M. aeruginosa PCC 7806 doubled its microcystin quota per cell as temperature decreased from 26°C to 19°C.
- The non-toxigenic mutant exhibited altered photo-physiology at 19°C, including increased electron sinks and non-photochemical quenching.
- The mutant showed increased expression of a glutathione-dependent peroxiredoxin, indicating ROS defense mechanisms.
Conclusions:
- Microcystin production may confer a selective advantage to M. aeruginosa under cold conditions by aiding in oxidative stress management.
- The wild-type strain's strategy of producing microcystin represents a long-term defense against oxidative stress.
- The mutant's response suggests a shorter-term, proactive strategy for dissipating or degrading oxidative stress agents in the absence of microcystin.
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