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. 2022 Apr 14;22(1):103.
doi: 10.1186/s12866-022-02519-9.

Cryopreservation of vegetative cells and zygotes of the multicellular volvocine green alga Gonium pectorale

Affiliations

Cryopreservation of vegetative cells and zygotes of the multicellular volvocine green alga Gonium pectorale

Hisayoshi Nozaki et al. BMC Microbiol. .

Erratum in

Abstract

Background: Colonial and multicellular volvocine green algae have been extensively studied recently in various fields of the biological sciences. However, only one species (Pandorina morum) has been cryopreserved in public culture collections.

Results: Here, we investigated conditions for cryopreservation of the multicellular volvocine alga Gonium pectorale using vegetative colonies or cells and zygotes. Rates of vegetative cell survival in a G. pectorale strain after two-step cooling and freezing in liquid nitrogen were compared between different concentrations (3% and 6%) of the cryoprotectant N,N-dimethylformamide (DMF) and two types of tubes (0.2-mL polymerase chain reaction tubes and 2-mL cryotubes) used for cryopreservation. Among the four conditions investigated, the highest rate of survival [2.7 ± 3.6% (0.54-10%) by the most probable number (MPN) method] was obtained when 2.0-mL cryotubes containing 1.0 mL of culture samples with 6% DMF were subjected to cryogenic treatment. Using these optimized cryopreservation conditions, survival rates after freezing in liquid nitrogen were examined for twelve other strains of G. pectorale and twelve strains of five other Gonium species. We obtained ≥ 0.1% MPN survival in nine of the twelve G. pectorale strains tested. However, < 0.1% MPN survival was detected in eleven of twelve strains of five other Gonium species. In total, ten cryopreserved strains of G. pectorale were newly established in the Microbial Culture Collection at the National Institute for Environmental Studies. Although the cryopreservation of zygotes of volvocine algae has not been previously reported, high rates (approximately 60%) of G. pectorale zygote germination were observed after thawing zygotes that had been cryopreserved with 5% or 10% methanol as the cryoprotectant during two-step cooling and freezing in liquid nitrogen.

Conclusions: The present study demonstrated that cryopreservation of G. pectorale is possible with 6% DMF as a cryoprotectant and 1.0-mL culture samples in 2.0-mL cryotubes subjected to two-step cooling in a programmable freezer.

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Conflict of interest statement

The authors declare that they have no competing interests.

Figures

Fig. 1
Fig. 1
Life cycle of Gonium pectorale. A Diagram of life cycle showing facultative sexual reproduction and heterothallic mating system. Based on Nozaki & Ito [21] and the present study. B Vegetative colonies of NIES-4502. C Mature zygotes ready for germination (NIES-4501 ×ばつ NIES-4502). D Successive stages of zygote germination showing release of a four-celled germ colony. All at same magnification. E Empty zygote walls after germination (NIES-4501 ×ばつ NIES-4502)
Fig. 2
Fig. 2
Effects of cryoprotectants on germination of Gonium pectorale zygotes (NIES-4501 ×ばつ NIES-4502) that were subjected to liquid nitrogen freezing (Table 4). A 5% methanol cryogenic treatment. Note empty zygote walls after germination. B 5% DMF cryogenic treatment. Note intact, walled zygotes
Fig. 3
Fig. 3
Five-day-old growth of Gonium pectorale progenies given rise from zygotes (NIES-4501 ×ばつ NIES-4502) that were subjected to liquid nitrogen freezing with six types of cryoprotectants. Compare these results with zygote germination rates (Table 4). A 5% DMSO. B 10% DMSO. C 5% methanol. D 10% methanol. E 5% DMF. F 10% DMF

References

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