Simple steps to enable reproducibility: culture conditions affecting Chlamydomonas growth and elemental composition.

Colleen Hui, Stefan Schmollinger, Daniela Strenkert, Kristen Holbrook, Hayden R Montgomery, Si Chen, Hosea M Nelson, Peter K Weber, Sabeeha S Merchant

Journal: The Plant journal : for cell and molecular biology 2022;111(4):995-1014

PMID: 35699388

Abstract

Even subtle modifications in growth conditions elicit acclimation responses affecting the molecular and elemental makeup of organisms, both in the laboratory and in natural habitats. We systematically explored the effect of temperature, pH, nutrient availability, culture density, and access to CO and O in laboratory-grown algal cultures on growth rate, the ionome, and the ability to accumulate Fe. We found algal cells accumulate Fe in alkaline conditions, even more so when excess Fe is present, coinciding with a reduced growth rate. Using a combination of Fe-specific dyes, X-ray fluorescence microscopy, and NanoSIMS, we show that the alkaline-accumulated Fe was intracellularly sequestered into acidocalcisomes, which are localized towards the periphery of the cells. At high photon flux densities, Zn and Ca specifically over-accumulate, while Zn alone accumulates at low temperatures. The impact of aeration was probed by reducing shaking speeds and changing vessel fill levels; the former increased the Cu quota of cultures, the latter resulted in a reduction in P, Ca, and Mn at low fill levels. Trace element quotas were also affected in the stationary phase, where specifically Fe, Cu, and Zn accumulate. Cu accumulation here depends inversely on the Fe concentration of the medium. Individual laboratory strains accumulate Ca, P, and Cu to different levels. All together, we identified a set of specific changes to growth rate, elemental composition, and the capacity to store Fe in response to subtle differences in culturing conditions of Chlamydomonas, affecting experimental reproducibility. Accordingly, we recommend that these variables be recorded and reported as associated metadata.

© 2022 Society for Experimental Biology and John Wiley & Sons Ltd.

Address: Department of Chemistry and Biochemistry, University of California, Los Angeles, CA, 90095, USA.; Chemical Sciences Division, Lawrence Livermore National Laboratory, Livermore, CA, 94550, USA.; California Institute for Quantitative Biosciences (QB3), University of California, Berkeley, CA, 94720, USA.; Advanced Photon Source, Argonne National Laboratory, Argonne, IL, 60439, USA.; Lawrence Livermore National Laboratory, Physical and Life Science Directorate, Livermore, CA, 94550, USA.; Department of Molecular and Cell Biology, University of California, Berkeley, CA, 94720, USA.; Department of Plant and Microbial Biology, University of California, Berkeley, CA, 94720, USA.
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