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Open AccessJournal ArticleDOI

Cell-free metabolic engineering: biomanufacturing beyond the cell.

TLDR
In the coming years, CFME will offer exciting opportunities to debug and optimize biosynthetic pathways, carry out design‐build‐test iterations without re‐engineering organisms, and perform molecular transformations when bioconversion yields, productivities, or cellular toxicity limit commercial feasibility.
Abstract
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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Citations
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Journal ArticleDOI

Artificial Biocatalytic Linear Cascades for Preparation of Organic Molecules

TL;DR: The review introduces a systematic classification of the cascades according to the number of enzymes in the linear sequence and differentiates between cascades involving exclusively enzymes and combinations of enzymes with non-natural catalysts or chemical steps.
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Portable, On-Demand Biomolecular Manufacturing

TL;DR: This paper presents a portable platform that provides the means for on-site, on-demand manufacturing of therapeutics and biomolecules and demonstrates the manufacture and functional validation of antimicrobial peptides and vaccines and presents combinatorial methods for the production of antibody conjugates and small molecules.
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Synthetic biology devices for in vitro and in vivo diagnostics

TL;DR: Current efforts in synthetic biology are described, focusing on the translation of promising technologies into pragmatic diagnostic tools and platforms, which could provide near real-time surveillance of multiple pathological conditions.

The future of metabolic engineering and synthetic biology: Towards a systematic practice

TL;DR: This work attempts to lay down a framework around which bioreaction engineering can systematize itself just like chemical reaction engineering, and introduces a new approach to engineering secondary metabolism known as 'multivariate modular metabolic engineering' (MMME), whose novelty lies in its assessment and elimination of regulatory and pathway bottlenecks by re-defining the metabolic network as a collection of distinct modules.
Journal ArticleDOI

Transforming the carbon economy: challenges and opportunities in the convergence of low-cost electricity and reductive CO2 utilization

TL;DR: In this paper, the authors assess and characterize the top technical barriers for utilizing renewable electricity for CO2 reduction across five different conversion approaches (direct electrochemical, direct bioelectrochemical, indirect non-thermal plasma, indirect bioelectron, and indirect thermochemical) under state-of-technology conditions, outline the R&D needs to overcome each barrier, and identify the most promising C1-C3 hydrocarbons and oxygenates based on their relative ease of formation, economic viability, CO2 utilization potential, and energy storage capacity.
References
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TL;DR: Applications of protein-engineered biocatalysts ranging from commodity chemicals to advanced pharmaceutical intermediates that use enzyme catalysis as a key step are discussed.
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Plasmofluidic single-molecule surface-enhanced Raman scattering from dynamic assembly of plasmonic nanoparticles

TL;DR: By utilizing dual excitation of plasmons at metal-fluid interface, this work creates interacting assemblies of metal nanoparticles, which may be further harnessed in dynamic lithography of dispersed nanostructures and have implications in realizing optically addressable, plasmofluidic, single-molecule detection platforms.
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