Challenges in developing microbes for industrial biotechnology · Challenges in developing...
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Challenges in developing microbes
for industrial biotechnology
Rishi Jain, Praj Matrix, India
10-Oct-2012
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Domains of life
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http://pacelab.colorado.edu/images/Big_Tree_Bold_Letters_white.png
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Bioprospecting
• Various environments
• Thermal springs
• Deep sea hydrothermal vents
• Polar regions
• Marine environments
• Forests
• Deserts
• Digestive tracts of animals
• Techniques
• Traditional cultivation
• Metagenomics
• Metatranscriptomics
• Metaproteomics
• Single cell genomics
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A) Metagenomics B) Metatranscriptomics
C) MetaproteomicsBiotechnol Lett. 2010 Oct;32(10):1351-9
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Economical scale-up
Contributors to Cost Stack
• Titers, Yield, Productivity
• Carbon source
• Nutrient requirements
• Sterility
• Down stream processing
• Power
• Water and carbon footprints
• Energy and heat
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Feedstock
• First generation sugars
• Mainly C6 sugars
• Sugarcane juice, Molasses, Beet, Cassava, Corn
• Second generation feedstocks
• Agricultural residues, Forest biomass, Grasses
• Polymers of C6 and C5 sugars
• Microbial growth Inhibitors – acetic acid, furans and phenols
• Strain development solutions
• Bioprospecting for microbes that efficiently convert C6 and C5 sugars to
product of interest
• Targeted strain engineering approaches to introduce pathways that can
efficiently utilize different types of sugars
• Classical mutagenesis used for overcoming inhibitor tolerances
• Reverse metabolic engineering
• Consolidated bioprocessing
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Nutrient requirements
Nutrients
• Nitrogen
• Phosphorus
• Sulfur
• Amino acids
• Vitamins
• Trace elements
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Industrial sources
• Corn steep liquor
• Corn steep powder
• Cotton seed meal
• Dry brewer’s yeast
• Distillery wastes
• Chicken Feather hydrolysate
• Strain development solutions
• Targeted engineering approaches for elimination of certain
auxotrophies
• Adaptation to industrial sources to overcome inhibitor
tolerances
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Downstream processing
• Extraction of product from the fermentation broth
• Product titers
• Intracellular / Extracellular
• Byproduct profile and concentrations
• Strain development solutions
• Targeted engineering approaches for increasing titers of the
product
• Mutagenesis and adaptation for increasing product tolerance
• Reduction of byproducts by targeted engineering approaches
• Targeted engineering approaches to expel intracellular products
of interest out of the cell
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Sterility requirements
• Highly engineered or mutated strain – growth rate
decreases
• Competitive edge over other wild-type strains decreases
• In case of contamination, batch losses may occur
• Strain development solutions
• Optimize the number of genetic changes
• Co-culture fermentation
• Synthetic biology for transitions between different physiological
states
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Metabolic engineering
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Nat Rev Microbiol. 2009 Feb;7(2):129-43Appl Microbiol Biotechnol. 2001 Apr;55(3):263-83
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Synthetic biology
• Rational design, construction & characterization of biological systems
• Assembling of basic biological components into larger networks
• Creation of standardized biological parts, devices and systems
• These biological components are interchangeable, functionally discrete and capable of being easily combined in a modular fashion
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Andrianantoandro, E., Mol. Sys. Biol., 2006 May
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Classical methods
• Complex targets that are not well understood at the
molecular level
• Product tolerance
• Growth inhibitor tolerance
• Thermotolerance
• Random mutagenesis
• Physical mutagens – UV rays, X-rays, etc
• Chemical mutagens – Ethidium bromide, N-methyl-N'-nitro-N-
nitrosoguanidine (NTG)
• Adaptation – Chemostat
• Hybrid approaches like site-directed mutagenesis and
combinatorial mutagenesis
• Reverse metabolic engineering
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Economics of
strain development
• Millions of dollars
• Interdisciplinary requirements
• High-end instrumentation
• Collaboration
• Industrial
• Academic
• Government support
• Funding
• Collaborative platforms
• Indo-Canadian
• Indo-US
• Indo-European
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Praj Focus Areas
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BioButanol
BioDiesel