A Bifunctional Polyphosphate Kinase Driving the Regeneration of Nucleoside Triphosphate and Reconstituted Cell-Free Protein Synthesis-Reference-Cited by-同舟云学术

A Bifunctional Polyphosphate Kinase Driving the Regeneration of Nucleoside Triphosphate and Reconstituted Cell-Free Protein Synthesis

Published:2019-12-12 Issue:1 Volume:9 Page:36-42
ISSN:2161-5063
Container-title:ACS Synthetic Biology
language:en
Short-container-title:ACS Synth. Biol.

Author:

Wang Po-Hsiang¹^ORCID,Fujishima Kosuke¹²^ORCID,Berhanu Samuel¹,Kuruma Yutetsu¹³,Jia Tony Z.¹⁴^ORCID,Khusnutdinova Anna N.⁵,Yakunin Alexander F.⁵⁶^ORCID,McGlynn Shawn E.¹⁴^ORCID

Affiliation:

1. Earth-Life Science Institute, Tokyo Institute of Technology, Tokyo, 152-8550, Japan

2. Graduate School of Media and Governance, Keio University, Fujisawa, 108-8345, Japan

3. JST, PRESTO, Saitama, 102-0076, Japan

4. Blue Marble Space Institute of Science, Seattle, Washington 98154, United States

5. Department of Chemical Engineering and Applied Chemistry, University of Toronto, Toronto, Ontario ON M5S, Canada

6. Centre for Environmental Biotechnology, Bangor University, Bangor, Wales LL57 2DG, United Kingdom

Funder

Genome Canada

Japan Society for the Promotion of Science

Natural Sciences and Engineering Research Council of Canada

National Science Foundation

FirstLogic-Astrobiology donation program

Publisher

American Chemical Society (ACS)

Subject

Biochemistry, Genetics and Molecular Biology (miscellaneous),Biomedical Engineering,General Medicine

Link

https://pubs.acs.org/doi/pdf/10.1021/acssynbio.9b00456

Reference30 articles.

1. ‘Unknown’ proteins and ‘orphan’ enzymes: the missing half of the engineering parts list – and how to find it

2. A cell-free protein synthesis system for high-throughput proteomics

3. Mimicking theEscherichia coli cytoplasmic environment activates long-lived and efficient cell-free protein synthesis

4. Preparative scale expression of membrane proteins in Escherichia coli-based continuous exchange cell-free systems

5. Synthesis of milligram quantities of proteins using a reconstituted in vitro protein synthesis system

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