How White Biotechnology Transforms Pharmacy with Microbes and Enzymes
Cellular Factories Converting Waste into Medicines
Imagine a microscopic factory that transforms plastic bottles into paracetamol. This isn't science fiction: it's white biotechnology, the discipline that uses living cells and enzymes to revolutionize pharmaceutical production. Today, more than 50% of essential drugs â from antibiotics to cancer therapies â depend on these biological processes. With an annual growth rate of 11.1% (2025-2035) 1 , this "molecular alchemy" promises purer, cheaper, and more sustainable medicines.
White biotechnology in pharma (2025-2035 projection)
The industrial branch of biotechnology uses living organisms (bacteria, yeast, fungi) or their enzymatic components to manufacture chemical products. In pharmacy, it stands out for:
White biotechnology leverages existing cellular machinery rather than creating synthetic pathways. As researcher Stephen Wallace notes: "Microbes already have the tools â we just need to direct their natural processes" 9 .
Based on the University of Edinburgh study (Nature, 2025) 9
Ground PET bottles are treated with thermostable hydrolases (isolated from Ideonella sakaiensis), breaking the plastic into terephthalic acid (TA).
The TA is exposed to modified Escherichia coli with genes from Pseudomonas putida, converting it to para-hydroxybenzoic acid (pHBA).
Intracellular phosphates from the bacteria catalyze the transformation of pHBA to para-aminophenol (PAP), the paracetamol precursor.
Native E. coli enzymes add acetyl groups to PAP, yielding pure paracetamol (99.2%).
Modified E. coli in bioreactor converting plastic waste to pharmaceuticals
Parameter | Traditional Chemical | White Biotech |
---|---|---|
Raw material | Crude oil | PET plastic waste |
Temperature | 150-200°C | 25-37°C |
Hazardous waste | Nitrous acid, cyanide | Water, biogenic COâ |
Product purity | ~95% | >99% |
Stage | Conversion | Time |
---|---|---|
PET â Terephthalic Acid | 98% | 24 h |
TA â pHBA | 85% | 12 h |
pHBA â PAP | 78% | 18 h |
PAP â Paracetamol | 99% | 6 h |
paracetamol per kg plastic
net COâ emissions
purity achieved
Key innovation: The bacteria already possessed the biochemical machinery; researchers simply redirected their metabolism through genetic engineering ("metabolic maps, not reprogramming") 9 .
Key materials to replicate the experiment or develop new pharmaceutical bioprocesses:
Reagent/Equipment | Function | Commercial Example |
---|---|---|
Modified E. coli strains | Metabolic chassis for biotransformations | E. coli BL21(DE3) with pET plasmids |
Thermostable hydrolases | Degrade plastics to monomers | PETase from Ideonella sakaiensis |
Serum-free culture media | Cell nutrition without contaminants | Gibco⢠CDM4HEK⢠|
Continuous flow bioreactors | Controlled fermentation with feedback | Sartorius BIOSTAT® STR |
Metabolome sensors | Real-time metabolite monitoring | YSI 2900 Series Analyzer |
Beta-defensin 38 | Bench Chemicals | |
Beta-defensin 36 | Bench Chemicals | |
Beta-defensin 33 | Bench Chemicals | |
Beta-defensin 14 | Bench Chemicals | |
Beta-defensin 13 | Bench Chemicals |
Essential equipment for white biotechnology research in pharmaceuticals
White biotechnology doesn't just produce drugs: it redefines pharmacy as a circular economy. Projects underway for 2030 include:
Converting COâ into chemotherapeutic agents 1
Designing enzymes to synthesize "impossible" molecules 6
Programmable bacteria generating insulin in the body 2
"Waste is carbon... and microbes love carbon."
In 2025, 325 million people already use drugs produced with white biotechnology . Your next painkiller could be born from a recycled bottle.