Affordable and Safe Microalgae secreted Growth Factors for Lab Grown Meat

Backed by Ethan
Orr Biologicals
Vista, California
Biology
$275
Pledged
4%
Funded
$8,850
Goal
5
Days Left
  • $275
    pledged
  • 4%
    funded
  • 5
    days left

About This Project

Fetal Bovine Serum or FBS is blood plasma containing essential growth factors needed for cells to turn into muscle tissue, the basis of lab grown meat. However, FBS carries the risk of bloodborne pathogens and comes at a premium cost, making lab grown meat unaffordable. We aim to solve this problem by making a genetically modified microalga to produce the same growth factors as in FBS, allowing for decreased costs, as well as faster and cleaner production of lab grown meat.

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What is the context of this research?

While meat consumption is essential for many to meet daily protein needs, the resource strain, environmental pitfalls, and animal suffering problems associated with conventionally produced meat are major causes for concern.

To make lab grown meat, FBS or fetal bovine serum, is required as an additive to grow cells, as it contains growth factors. These growth factors are the essential components of FBS and are needed for cell growth. We aim to replace FBS with just growth factors.

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.

This means the DNA of the microalgae is altered to produce the growth factors.

Epidermal Growth Factor is a successful example of a growth factor that was secreted by microalgae. Using the algae derived growth factors, we can create a 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.

Furthermore, animal suffering can be reduced, as if lab grown meat is made cheaper and safely, the need of slaughtering becomes irrelevant. While microalgae grow and produce the growth factors, they also sequester co2 while exhaling oxygen, crucial for a net carbon zero workplace.

Our project is significant because it helps lay the groundwork for future scientists to expand in the cultivated meat community due to the lower costs needed to run experiments, leading to more innovation. We truly believe that lab grown meat can be the future if this project is funded.

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

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This budget is needed to help execute my experiment. In the additional details at the bottom of the page, there is a list of things I will buy. This is a very comprehensive list of materials.


Endorsed by

Cameron’s projects address a critical challenge in the future of food systems by exploring how algae derived growth factors can support the proliferation of chicken muscle cells, a key step toward making cultivated meat more affordable and accessible. This work is innovative and demonstrates a strong understanding of cellular biology and its real-world applications. Although Cameron is early in his academic career, he is at the top of his biology class and consistently shows exceptional intellect, curiosity, and drive.
I look forward to seeing the development of this project. I believe it will address crucial disparities within the lab-grown meat industry, corresponding prices, and ethical considerations regarding animals taking part in the process. Cameron has had significant experience thus far in the laboratory setting, demonstrating a commitment that will be useful to the successful completion of his experiment.
I am excited about the possibility of producing such expensive compounds in relatively simple and efficient organisms! This has many implications for not only cultivated meat but cell culture in general, reducing costs in things like stem cell therapy.

Meet the Team

Cameron Orr
Cameron Orr

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

Below is the media and growth factors we will make microalgae secrete.


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

EGF, Chicken - GenScript

Albumin, Chicken

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


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