4.5 Review

Cell-free metabolic engineering: Biomanufacturing beyond the cell

Journal

BIOTECHNOLOGY JOURNAL
Volume 10, Issue 1, Pages 69-82

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/biot.201400330

Keywords

Biocatalysis; Biotransformation; Cell-free metabolic engineering; Metabolic pathway debugging; Synthetic biology

Funding

  1. National Science Foundation [MCB-0943393]
  2. Office of Naval Research [N00014-11-1-0363]
  3. DARPA YFA Program [N66001-11-1-4137]
  4. Army Research Office [W911NF- 11-1-044]
  5. NSF Materials Network Grant [DMR - 1108350]
  6. DARPA Living Foundries Program [N66001-12-C-4211]
  7. David and Lucile Packard Foundation [2011-37152]
  8. ARPA-E [DE-AR0000435]
  9. Chicago Biomedical Consortium
  10. Searle Funds at the Chicago Community Trust
  11. Northwestern Molecular Biophysics Training Program - NIH via NIGMS [5T32 GM008382]
  12. Division Of Materials Research
  13. Direct For Mathematical & Physical Scien [1108350] Funding Source: National Science Foundation

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Industrial biotechnology and microbial metabolic engineering are poised to help meet the growing demand for sustainable, low-cost commodity chemicals and natural products, yet the fraction of biochemicals amenable to commercial production remains limited. Common problems afflicting the current state-of-the-art include low volumetric productivities, build-up of toxic intermediates or products, and byproduct losses via competing pathways. To overcome these limitations, cell-free metabolic engineering (CFME) is expanding the scope of the traditional bioengineering model by using in vitro ensembles of catalytic proteins prepared from purified enzymes or crude lysates of cells for the production of target products. In recent years, the unprecedented level of control and freedom of design, relative to in vivo systems, has inspired the development of engineering foundations for cell-free systems. These efforts have led to activation of long enzymatic pathways (>8 enzymes), near theoretical conversion yields, productivities greater than 100 mg L-1 h(-1), reaction scales of >100 L, and new directions in protein purification, spatial organization, and enzyme stability. In the coming years, CFME will offer exciting opportunities to: (i) debug and optimize biosynthetic pathways; (ii) carry out design-build-test iterations without re-engineering organisms; and (iii) perform molecular transformations when bioconversion yields, productivities, or cellular toxicity limit commercial feasibility.

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