Priming of microcystin degradation in carbon-amended membrane biofilm communities is promoted by oxygen-limited conditions

FEMS Microbiol Ecol. 2019 Nov 1;95(11):fiz157. doi: 10.1093/femsec/fiz157.

Abstract

Microbial biofilms are an important element of gravity-driven membrane (GDM) filtration systems for decentralized drinking water production. Mature biofilms fed with biomass from the toxic cyanobacterium Microcystis aeruginosa efficiently remove the cyanotoxin microcystin (MC). MC degradation can be 'primed' by prior addition of biomass from a non-toxic M. aeruginosa strain. Increased proportions of bacteria with an anaerobic metabolism in M. aeruginosa-fed biofilms suggest that this 'priming' could be due to higher productivity and the resulting changes in habitat conditions. We, therefore, investigated GDM systems amended with the biomass of toxic (WT) or non-toxic (MUT) M. aeruginosa strains, of diatoms (DT), or with starch solution (ST). After 25 days, these treatments were changed to receiving toxic cyanobacterial biomass. MC degradation established significantly more rapidly in MUT and ST than in DT. Oxygen measurements suggested that this was due to oxygen-limited conditions in MUT and ST already prevailing before addition of MC-containing biomass. Moreover, the microbial communities in the initial ST biofilms featured high proportions of facultative anaerobic taxa, whereas aerobes dominated in DT biofilms. Thus, the 'priming' of MC degradation in mature GDM biofilms seems to be related to the prior establishment of oxygen-limited conditions mediated by higher productivity.

Keywords: bacteria; biofilms; habitat priming; microbial communities; microcystin degradation; oxygen-limited conditions.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bacterial Toxins / metabolism*
  • Biofilms*
  • Biomass
  • Carbon / metabolism
  • Diatoms / metabolism
  • Microcystins / metabolism*
  • Microcystis / metabolism
  • Oxygen / metabolism*

Substances

  • Bacterial Toxins
  • Microcystins
  • Carbon
  • microcystin
  • Oxygen