What are the 4 key impacts of bioprocesses
chemoorganoheterotroph
Antibiotic targets and clinical examples
Cell wall synthesis (peptidoglycan)
- Penicillin, Vancomycin, Bacitracin
DNA replication / transcription
- Ciprofloxacin (DNA), Rifampicin (RNA)
Protein synthesis (translation)
- Streptomycin, Tetracycline, Erythromycin, Chloramphenicol
Cell membrane integrity
- Polymyxin B
Energy production
- Daptomycin
bacterial producers of antibiotics
(don’t need to know specifics; Streptomyces species is most commonly used)
Streptomyces griseus
- Streptomycin, ~500,000 tons/yr, Tuberculosis
Streptomyces aureofaciens
- Tetracycline, ~300,000 tons/yr, Broad-spectrum; human &
veterinary medicine
Bacillus subtilis
- Bacitracin, ~10,000 tons/yr, Topical skin infections
Streptomyces venezuelae
- Chloramphenicol, ~1,000 tons/yr, Broad-spectrum (limited use due to side effects)
Streptomyces erythreus
- Erythromycin ~5,000 tons/yr, Respiratory & skin infections
fungal producers of antibiotics
(don’t need to know specifics; penicillium is most commonly used)
Penicillium chrysogenum
- Penicillin, ~70,000 tons/yr, First discovered antibiotic; bacterial infections
Cephalosporium acremonium
- Cephalosporin, ~30,000 tons/yr, Beta-lactam; broad range of
infections
Aspergillus nidulans
-Griseofulvin, ~500 tons/yr, Antifungal; skin & nail infections
Tolypocladium inflatum
- Cyclosporin, ~1,000 tons/yr, Immunosuppressant; organ
transplants
Fusarium spp.
- Fusidic Acid ~100 tons/yr Staphylococcus aureus skin
infections
what were the first antibiotics used
G + or G - allows more uptake of antibiotics
G +
Bioprospecting
searching natural environments (soil, water, food) for organisms that produce valuable
metabolites (antibiotics)
method: soil particles are placed on plates inoculated with target bacteria. A clear ‘halo’ (zone of inhibition) around a soil particle indicates the presence of an antibiotic-producing microorganism
ex. A halo around soil on a Staphylococcus epidermidis plate (Gram+) but not an E. coli plate
(Gram−) suggests a Gram-positive-specific antibiotic.
primary metabolite
byproduct of metabolism produced during active growth phase; essential to the organism’s survival.
Examples: ethanol, lactic acid, amino acids. Production parallels cell growth.
Secondary Metabolites
byproduct of metabolism produced after active growth slows; NOT essential to growth. Often produced as defense compounds.
Examples: penicillin, many antibiotics. Production
begins as cell growth plateaus.
Aspergillus niger
strain improvement
Wild-type microorganisms rarely produce metabolites in industrial quantities. Scientists improve strains through:
* Artificial selection for mutants that overproduce the desired metabolite.
* Genetic engineering — cloning metabolite-synthesis genes into easier-to-culture organisms like E. coli.
* Design–Build–Test–Learn cycles to iteratively optimize production strains.
Scale-up
-Translating lab-scale microbial production to industrial quantities requires careful scale-up. The process moves
through three stages:
Laboratory fermenter (~15 L): tests nutrients, temperature, oxygen levels, pH.
* Pilot plant fermenter (~1,000 L): refines conditions identified at lab scale.
* Large industrial fermenter (>1,000 L): full commercial production in large stainless-steel vessels.
Key components of an industrial fermenter
impellers for mixing, aeration (sterile air bubbled through the
medium), pH monitors, cooling jackets, and nutrient/exhaust ports. After fermentation, the metabolite is recovered
by filtration, settling, or centrifugation, then dried or purified
other microbially produced pharmaceuticals
Pravastatin
- Lowering cholesterol, Penicillium citrinum (fungus)
Cyclosporin
- Prevents organ rejection in transplant patients, Tolypocladium inflatum (fungus)
Ergot alkaloids
- Induction of labor, Claviceps purpurea (fungus)
Mitomycin
- Anti-cancer drug, Streptomyces caespitosus (bacterium)
Cortisone
- Pain and inflammation, Rhizopus nigricans (fungus) —bioconversion
Progesterone
- Prevent miscarriage Rhizopus nigricans — bioconversion
Proteases
microbial enzyme, digest proteins; used in meat tenderizers, drain cleaners, and laundry detergents (removing
blood or food stains)
Cellulases
microbial enzymes, break down cellulose into sugars; used in detergents to remove grass stains
extremozymes
(e.g., Taq polymerase): enzymes from extremophiles that function under extreme
conditions. Taq polymerase is derived from Thermus aquaticus (a thermophile) and is essential for PCR in clinical diagnostics and research
biopesticides
Bacillus thuringiensis (Bt) produces crystalline protein toxins that are lethal to specific insect larvae (moth and mosquito larvae) but harmless to humans and other animals.
* The bacterium forms endospores containing the toxin. When ingested by the target insect, the toxin destroys the digestive system and kills the larva.
* Bt spores are cultured in fermenters, harvested, and sold as biological pest control agents — an alternative to synthetic chemical pesticides
bioremediation
the use of living organisms — primarily bacteria and fungi — to degrade or neutralize
environmental pollutants. It is a natural process that is often cheaper, safer, and more effective than chemical or physical cleanup methods
Bacterial bioremediation
Oil spills: hydrocarbon-degrading bacteria (methanotrophs, heterotrophs, chemotrophs) break down
petroleum components (methane, ethane, octane) into CO2 and water.
* Dispersants break oil into smaller droplets, increasing bacterial surface area for degradation.
* Adding nitrogen and phosphorus nutrients stimulates bacterial growth and accelerates cleanup.
mycoremediation
composting
safety and industrial microorganisms
Industrial microorganisms must be safe for humans and the environment.
* Pathogens are never used in industrial applications, even if they produce valuable metabolites.
* Most industrial strains are highly specialized (‘domesticated’) and are unlikely to survive outside the
fermenter.
* Rigorous safety testing is required before any microorganism is used in commercial production