Chlorella vulgaris has been proposed as a promising green alga for CO2 biomitigation due to its attractive traits of
high growth rate, excellent CO2 fixation ability and broad industrial applications. Nevertheless, the genetic engineering
of this alga is still in its infancy. In the present study, a stable and efficient transformation system was
established for C. vulgaris CBS 15-2075, a robust strain with great potential for CO2 biomitigation. The antibiotic
sensitivity spectrum of this organism was evaluated, and the nptII gene was selected as a dominant selectable
marker for genetic transformation. The selectable marker, together with an enhanced green fluorescent protein
(EGFP) gene, was delivered into C. vulgaris protoplasts by using a PEG-mediated method, giving a transformation
efficiency of 356 ± 30 cfu per μg vector DNA. Molecular characterization and live-cell fluorescence microscopy
demonstrated that the EGFP gene was stably integrated into C. vulgaris genome and expressed in the cytoplasm
of transformed cells. Taken together, we for the first time established a stable and useful genetic toolkit for the
industrially important microalga C. vulgaris, which will facilitate to a great extent the future rational genetic manipulation
for strain improvement to increase CO2 fixation capacity and may as well provide valuable insights
into other Chlorella species. Besides, the success in EGFP expression and live-cell fluorescence detection in
C. vulgaris will be useful in molecular and cell biology for protein subcellular localization
Chlorella vulgaris has been proposed as a promising green alga for CO2 biomitigation due to its attractive traits ofhigh growth rate, excellent CO2 fixation ability and broad industrial applications. Nevertheless, the genetic engineeringof this alga is still in its infancy. In the present study, a stable and efficient transformation system wasestablished for C. vulgaris CBS 15-2075, a robust strain with great potential for CO2 biomitigation. The antibioticsensitivity spectrum of this organism was evaluated, and the nptII gene was selected as a dominant selectablemarker for genetic transformation. The selectable marker, together with an enhanced green fluorescent protein(EGFP) gene, was delivered into C. vulgaris protoplasts by using a PEG-mediated method, giving a transformationefficiency of 356 ± 30 cfu per μg vector DNA. Molecular characterization and live-cell fluorescence microscopydemonstrated that the EGFP gene was stably integrated into C. vulgaris genome and expressed in the cytoplasmof transformed cells. Taken together, we for the first time established a stable and useful genetic toolkit for theindustrially important microalga C. vulgaris, which will facilitate to a great extent the future rational genetic manipulationfor strain improvement to increase CO2 fixation capacity and may as well provide valuable insightsinto other Chlorella species. Besides, the success in EGFP expression and live-cell fluorescence detection inC. vulgaris will be useful in molecular and cell biology for protein subcellular localization
การแปล กรุณารอสักครู่..
