Establishing the green algae Chlamydomonas incerta as a platform for recombinant protein production
Kalisa KangiD, Évellin do Espirito SantoiD, Crisandra Jade DiaziD, Aaron OliveriD, Lisa Saxton, Lauren MayiD, Stephen Patrick MayfieldiD, João Vitor Dutra MolinoiD
Abstract
Chlamydomonas incerta, a genetically close relative of the model green alga Chlamydomonas reinhardtii, shows significant potential as a host for recombinant protein expression. Because of the close genetic relationship between C. incerta and C. reinhardtii, this species offers an additional reference point for advancing our understanding of photosynthetic organisms, and also provides a potential new candidate for biotechnological applications. This study investigates C. incertas capacity to express three recombinant proteins: the fluorescent protein mCherry, the hemicellulose-degrading enzyme xylanase, and the plastic-degrading enzyme PHL7. We have also examined the capacity to target protein expression to various cellular compartments in this alga, including the cytosol, secretory pathway, cytoplasmic membrane, and cell wall. When compared directly with C. reinhardtii, C. incerta exhibited a distinct but notable capacity for recombinant protein production. Cellular transformation with a vector encoding mCherry revealed that C. incerta produced approximately 3.5 times higher fluorescence levels and a 3.7-fold increase in immunoblot intensity compared to C. reinhardtii. For xylanase expression and secretion, both C. incerta and C. reinhardtii showed similar secretion capacities and enzymatic activities, with comparable xylan degradation rates, highlighting the industrial applicability of xylanase expression in microalgae. Finally, C. incerta showed comparable PHL7 activity levels to C. reinhardtii, as demonstrated by the in vitro degradation of a polyester polyurethane suspension, Impranil(R) DLN. Finally, we also explored the potential of cellular fusion for the generation of genetic hybrids between C. incerta and C. reinhardtii as a means to enhance phenotypic diversity and augment genetic variation. We were able to generate genetic fusion that could exchange both the recombinant protein genes, as well as associated selectable marker genes into recombinant offspring. These findings emphasize C. incertas potential as a robust platform for recombinant protein production, and as a powerful tool for gaining a better understanding of microalgal biology. GRAPHICAL ABSTRACT O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=126 SRC="FIGDIR/small/618925v1_ufig1.gif" ALT="Figure 1"> View larger version (25K): org.highwire.dtl.DTLVardef@173d398org.highwire.dtl.DTLVardef@148ad36org.highwire.dtl.DTLVardef@63b5e9org.highwire.dtl.DTLVardef@3be081_HPS_FORMAT_FIGEXP M_FIG C_FIG
02 /Specification & Classification
Click any tag to browse matching papers- Citations
- 3
- FWCI
- 1.15
- Field percentile
- top 29%
- Organism
- Assay
- Research Focus
- Approach
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Sustainable production of plastic-degrading enzymes in Chlamydomonas pacifica
Crisandra Jade Diaz, João Vitor Dutra Molino, … Stephen Patrick Mayfield·bioRxiv·May 14, 2025
- Combinatorial engineering for photoautotrophic production of recombinant products from the green microalga Chlamydomonas reinhardtii
M. N. Abdallah, G. B. Wellman, … K. J. Lauersen·bioRxiv·Feb 28, 2022
- Successful establishment of an exogenous gene expression system in Chlamydomnas chloroplast based on viral replication elements
Yanan Jiang, Guiying Zhang, … Zhangli Hu·bioRxiv·Nov 26, 2024
- Towards a biotechnological platform for the production of human pro-angiogenic growth factors in the green alga Chlamydomonas reinhardtii
M. Jarquin Cordero, M. N. Chavez, … J. Nickelsen·bioRxiv·Nov 12, 2019
- Marchantia polymorpha as a simple platform for plant-based production of functional nanobodies
Sze Wai Tse, Facundo Romani, … Jim P. Haseloff·bioRxiv·Jun 23, 2026
- Engineering microalgal cell wall-anchored proteins using GP1 PPSPX motifs and releasing with intein-mediated fusion
Kalisa Kang, Évellin do Espirito Santo, … João Vitor Dutra Molino·bioRxiv·Jan 23, 2025