About This Project
The biggest barrier to making cultivated meat affordable is the prohibitive cost of fetal bovine serum and growth factors. In this proof of concept, we want to verify that microalgae produced growth factors can be integrated into a chemically defined medium to culture chicken cells. This way, my research hopes to create an alternative to fetal bovine serum, a common yet expensive media additive, to help in the proliferation and differentiation of chicken muscle satellite cells.
Ask the Scientists
Join The DiscussionWhat is the context of this research?
I am a high school freshman investigating the potential of producing cheap growth factors from microalgae that can benefit cell culture communities. For context, when cultivating cells for lab grown meat, an additive called fetal bovine serum (FBS) is used to maintain cell growth with growth factors. However, the use of FBS raises regulatory concerns due to contamination and ethical worries, as it comes from cow fetuses. Our experiment hopes to validate and prove the possibility of using recombinant algae produced growth factors in culture medium used to cultivate lab grown meat. Epidermal Growth Factor which is a growth factor we plan to express in our vector has been successfully demonstrated in the algae C. Reinhardtii. Using the algae derived growth factors, we can create a chemically defined media without unknown proteins that is significantly cheaper, ethical, and safe than FBS.
What is the significance of this project?
Using algal-expressed growth factors, the costs of media can be drastically reduced, as algae grow quickly and pose a vastly lower contamination risk when compared to fetal bovine serum. Our project is significant because it provides a proof of concept that growth factors can be expressed in microalgae, serving as a way to produce ethical and safe cultivated meat. Basically, we will discover whether it is feasible to express growth factors in microalgae for lab grown meat. We want this experiment to be a pilot study observing the effects of this algal derived FBS replacement for lab grown meat and myotube formation. However, this experiment is not just for cultivated meat; FBS is used in nearly every cell culture practice ranging from vaccine production to cancer research. What this means is that the removal of FBS and replacement with algae derived mitogenic compounds reduces costs in many areas of tissue culture research, which in turn allows for more innovations.
What are the goals of the project?
We will use a plasmid encoding for the growth factors we want to express and insert it into a cell wall deficient stain of C. Reinhardtii algae in the chloroplasts. The transformation will be done with acid washed glass beads inside a vortex mixer suspended in polyethylene glycol. After the microalgae secrete enough growth factors, we will purify the proteins with a gravity his tag column. In order to evaluate whether our growth factors are bioactive, we will attempt to cultivate chicken muscle satellite cells using the secreted growth factors and observe morphological characteristics to assess success. Furthermore, a ELISA will be ordered to measure any secreted growth factors.
Budget
Most of the funds utilized in this experiment are allocated to the DNA synthesis services, equipment, and reagents. Each and every item here is essential for this experiment. We decided to use scaled down or DIY equipment such as a co2 humidified incubator to allocate funds to must haves. It will be fully functioning however; I have experience in making bacteriological incubators. Furthermore, my school provides some essential cell culture equipment; centrifuges, some flasks, gel electrophoresis, and warm water baths. For equipment like the Co2 Incubator and the flow hood, these will also be used for future experiments in tissue culture or algal biotechnology, helping me in my journey in the biology world. Expensive items will be listed at the very bottom in the additional info section. Keep in mind I also account for discounts or shipping fees.
The Chicken Muscle Satellite Cells were from here Chicken Satellite Cells
Endorsed by
Project Timeline
We hope to immediately start the project right after funding. We expect to receive the DNA required for transformation in 7 business days. Following this, we can transform the microalgae and let it grow 12:12 day night cycle to reach optimal protein expression levels. From there, we will collect and lyse the microalgae before purifying. Then it will be sent for a protein assay and used for cell culture. For the cell culture, we plan to grow the cells control and variable simultaneously.
Jan 11, 2026
Project Launched
Feb 03, 2026
Receive DNA and transform C. Reinhardtii
Feb 06, 2026
Assays
Feb 10, 2026
Collect data: morphology,
Feb 12, 2026
Present data
Meet the Team
Cameron Orr
A freshman in high school that focuses on multidisciplinary biology subjects. Took 3 UCSD online extension courses in biology and microbiology, does research on articles, especially concerning algal biotech and tissue culture. I am very interested in the potential of organisms like algae for utilization in tissue culture. Furthermore, I also took in person tissue culture and biotechnology labs with Mira Costa.
Unfortunately, as a freshman, many opportunities such as internships are difficult to come by because of age restrictions. However, I do have experience in a lab setting working with chicken stem cell isolation from adipose tissue. As previously mentioned, I do have access to mentorship via some teachers and even a few from the workforce.
Additional Information
I also would like to meet some of you who are specialists in the field of tissue culture or related subjects to be my mentors. Backer benefits include online access to our finalized results, and your name displayed on our rolling credits in our YouTube videos.
In order to proliferate the cells, it will be in a Co2 Humidified Incubator 5% co2 32 degrees Celsius on T75 flasks and spinner flasks.
FORMULATIONS WE WILL TEST
DMEM 500mL
Chicken Albumin 0.05 ml/ml —
Epidermal Growth Factor (recombinant algae) 10 ng/ml —
Basic Fibroblast Growth Factor/FGF-2 (recombinant algae) 1 ng/ml —
Insulin (recombinant algae) 10 μg/ml 10 μg/ml
Dexamethasone (omitted)
This is the commercial proliferation media
The Odin chicken culture media (NOT TESTING, REFERENCE)
L15/F12 base 100mL
Streptomycin 50ug/mL
Gentamicin 50ug/mL
Ampicillin 100ug/mL
Amphotericin B 2ug/mL
20% Fetal Bovine Serum
FGF2 10ng/mL recomb. algae
EGF 10ng/mL recomb. algae
DTBIF MEDIA (MAIN ONE) After proliferation, we will switch to same media but without fgf-2 and EGF
DMEM 500mL
insulin (10 µg/ml)
transferrin (30 µg/ml)
FGF-2 (10 ng/ml)
1 mg/ml BSA- adjusted to albumin (chick) in our independent variable
EGF 10ng/mL (experimental, will test without first)
Sodium Selenite 2ng/mL (experimental, is important to suppress fibroblast growth and can be found in trace amounts to be sufficient. However, it is needed for stable lines especially passaging to lab grown meat.
We start with muscle satellite cells, which will be transformed into myoblasts, then to myocytes and myotubes.
Sales List
Recombinant Chicken Fibroblast Growth Factor 2, Basic (FGF2), N-His - BioVenic
Sodium selenite BioReagent, cell culture mammalian, = 98 10102-18-8
Conalbumin BioReagent, cell culture mammalian 1391-06-6
Chicken EGF Recombinant Protein | Kingfisher Biotech
Insulin from bovine pancreas Cell culture grade Sigma
https://bicellscientific.com/p... Protein Purification
Geneticin™ Selective Antibiotic (G418 Sulfate) (50 mg/mL) 20 mL | Buy Online | Gibco™
Gallus gallus fibroblast growth factor 2 (FGF2), mRNA - Nucleotide - NCBI
Project Backers
- 2Backers
- 1%Funded
- $25Total Donations
- $12.50Average Donation




