A downstream box fusion allows stable accumulation of a bacterial cellulase in Chlamydomonas reinhardtii chloroplasts.

Autor: Richter LV; 1Department of Biological and Environmental Engineering, Cornell University, 111 Wing Drive, Ithaca, NY USA., Yang H; 1Department of Biological and Environmental Engineering, Cornell University, 111 Wing Drive, Ithaca, NY USA.; 2Department of Molecular Biology and Genetics, Cornell University, Biotechnology Building, Ithaca, NY USA., Yazdani M; 1Department of Biological and Environmental Engineering, Cornell University, 111 Wing Drive, Ithaca, NY USA., Hanson MR; 2Department of Molecular Biology and Genetics, Cornell University, Biotechnology Building, Ithaca, NY USA., Ahner BA; 1Department of Biological and Environmental Engineering, Cornell University, 111 Wing Drive, Ithaca, NY USA.
Jazyk: angličtina
Zdroj: Biotechnology for biofuels [Biotechnol Biofuels] 2018 May 10; Vol. 11, pp. 133. Date of Electronic Publication: 2018 May 10 (Print Publication: 2018).
DOI: 10.1186/s13068-018-1127-7
Abstrakt: Background: We investigated strategies to improve foreign protein accumulation in the chloroplasts of the model algae Chlamydomonas reinhardtii and tested the outcome in both standard culture conditions as well as one pertinent to algal biofuel production. The downstream box (DB) of the TetC or NPTII genes, the first 15 codons following the start codon, was N -terminally fused to the coding region of cel6A , an endoglucanase from Thermobifida fusca . We also employed a chimeric regulatory element, consisting of the 16S rRNA promoter and the atpA 5'UTR, previously reported to enhance protein expression, to regulate the expression of the TetC- cel6A gene. We further investigated the accumulation of TetC-Cel6A under N -deplete growth conditions.
Results: Both of the DB fusions improved intracellular accumulation of Cel6A in transplastomic C. reinhardtii strains though the TetC DB was much more effective than the NPTII DB. Furthermore, using the chimeric regulatory element, the TetC-Cel6A protein accumulation displayed a significant increase to 0.3% total soluble protein (TSP), whereas NPTII-Cel6A remained too low to quantify. Comparable levels of TetC- and NPTII- cel6A transcripts were observed, which suggests that factors other than transcript abundance mediate the greater TetC-Cel6A accumulation. The TetC-Cel6A accumulation was stable regardless of the growth stage, and the transplastomic strain growth rate was not altered. When transplastomic cells were suspended in N -deplete medium, cellular levels of TetC-Cel6A increased over time along with TSP, and were greater than those in cells suspended in N -replete medium.
Conclusions: The DB fusion holds great value as a tool to enhance foreign protein accumulation in C. reinhardtii chloroplasts and its influence is related to translation or other post-transcriptional processes. Our results also suggest that transplastomic protein production can be compatible with algal biofuel production strategies. Cells displayed a consistent accumulation of recombinant protein throughout the growth phase and nitrogen starvation, a strategy used to induce lipid production in algae, led to higher cellular heterologous protein content. The latter result is contrary to what might have been expected a priori and is an important result for the development of future algal biofuel systems, which will likely require co-products for economic sustainability.
Databáze: MEDLINE
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