Abstract

The stramenopile alga Nannochloropsis evolved by secondary endosymbiosis of a red alga by a heterotrophic host cell and emerged as a promising organism for biotechnological applications, such as the production of polyunsaturated fatty acids and biodiesel. Peroxisomes play major roles in fatty acid metabolism but experimental analyses of peroxisome biogenesis and metabolism in Nannochloropsis are not reported yet. In fungi, animals, and land plants, soluble proteins of peroxisomes are targeted to the matrix by one of two peroxisome targeting signals (type 1, PTS1, or type 2, PTS2), which are generally conserved across kingdoms and allow the prediction of peroxisomal matrix proteins from nuclear genome sequences. Because diatoms lost the PTS2 pathway secondarily, we investigated its presence in the stramenopile sister group of diatoms, the Eustigmatophyceae, represented by Nannochloropsis. We detected a full-length gene of a putative PEX7 ortholog coding for the cytosolic receptor of PTS2 proteins and demonstrated its expression in Nannochloropsis gaditana. The search for predicted PTS2 cargo proteins in N. gaditana yielded several candidates. In vivo subcellular targeting analyses of representative fusion proteins in different plant expression systems demonstrated that two predicted PTS2 domains were indeed functional and sufficient to direct a reporter protein to peroxisomes. Peroxisome targeting of the predicted PTS2 cargo proteins was further confirmed in Nannochloropsis oceanica by confocal and transmission electron microscopy. Taken together, the results demonstrate for the first time that one group of stramenopile algae maintained the import pathway for PTS2 cargo proteins. To comprehensively map and model the metabolic capabilities of Nannochloropsis peroxisomes, in silico predictions needs to encompass both the PTS1 and the PTS2 matrix proteome.

Highlights

  • Peroxisomes are small organelles of 0.1–1.7 μm in diameter, surrounded by a single membrane and able to detoxify reactive oxygen species generated by diverse peroxisomal enzymes

  • Experimental studies investigating peroxisome biogenesis and functions are presently restricted to the diatom Phaeodactylum, which was shown to lack the PTS2 import pathway (Gonzalez et al, 2011)

  • Orthologs of most A. thaliana PEX proteins were identified in N. gaditana (Supplementary Table 1), suggesting that the fundamental mechanisms of peroxisome biogenesis and proliferation are largely conserved in Eustigmatophyceae

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Summary

Introduction

Peroxisomes are small organelles of 0.1–1.7 μm in diameter, surrounded by a single membrane and able to detoxify reactive oxygen species generated by diverse peroxisomal enzymes. Common peroxisomal functions of animals and plants are the glyoxylate cycle, amino acid metabolism, and polyamine oxidation. While in animals fatty acid β-oxidation occurs in both mitochondria and peroxisomes (Wanders and Waterham, 2006), in plants the process takes place exclusively in peroxisomes (Graham and Eastmond, 2002). Peroxisomal metabolism determines the steady state levels of total cellular fatty acids. Peroxisomes are involved in the biosynthesis of docosahexaenoic acid (C22:6n-3) and eicosapentaenoic acid (EPA; C20:5n-3) by partial degradation of polyunsaturated fatty acids (PUFAs) with longer chains, such as C24:6n-3 (Sprecher, 2000). Knowledge of the metabolic capabilities of peroxisomes from plants, yeast, and fungi in lipid metabolism is prerequisite for successful biotechnological applications and genetic engineering to increase PUFA and biodiesel productivity

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