Repository logo
Log in(current)
Repository logoMIT Open ScholarshipDSpace@MIT
  1. Home
  2. MIT Open Access Articles
  3. MIT Open Access Articles
  4. Bacterial Carbon Storage to Value Added Products

Bacterial Carbon Storage to Value Added Products

Thumbnail Image
Download
Name

Sinskey_Bacterial carbon.pdf

Size

1.98 MB

Format

Adobe PDF

Checksum (MD5)

f50d034a2dde458abeac8287bfdbcc5e

Author(s)
Brigham, Christopher J.
•
Kurosawa, Kazuhiko
•
Rha, Chokyun
•
Sinskey, Anthony J
Date Issued
December 2011
Journal
Journal of Microbial and Biochemical Technology
Publisher
OMICS Publishing Group
Citation
Brigham, Christopher J. et al. “Bacterial Carbon Storage to Value Added Products.” Applied Microbiology and Biotechnology 83 (2011). © 2011 OMICS Group
Version
Final published version
Abstract
PhaR from Paracoccus denitrificans functions as a repressor or autoregulator of the expression of genes encoding phasin protein (PhaP) and PhaR itself, both of which are components of polyhydroxyalkanoate (PHA) granules (A. Maehara, S. Taguchi, T. Nishiyama, T. Yamane, and Y. Doi, J. Bacteriol. 184:3992-4002, 2002). PhaR is a unique regulatory protein in that it also has the ability to bind tightly to an effector molecule, PHA polyester. In this study, by using a quartz crystal microbalance, we obtained direct evidence that PhaR binds to the target DNA and poly[(R)-3-hydroxybutyrate] [P(3HB)], one of the PHAs, at the same time. To identify the PhaR amino acid residues responsible for DNA binding, deletion and PCR-mediated random point mutation experiments were carried out with the gene encoding the PhaR protein. PhaR point mutants with decreased DNA-binding abilities were efficiently screened by an in vivo monitoring assay system coupled with gene expression of green fluorescent protein in Escherichia coli. DNA-binding abilities of the wild-type and mutants of recombinant PhaR expressed in E. coli were evaluated using a gel shift assay and a surface plasmon resonance analysis. These experiments revealed that basic amino acids and a tyrosine in the N-terminal region, which is highly conserved among PhaR homologs, are responsible for DNA binding. However, most of the mutants with decreased DNA-binding abilities were unaffected in their ability to bind P(3HB), strongly suggesting that PhaR has two separate domains capable of binding to the target DNA and P(3HB).
MIT Department
Harvard University--MIT Division of Health Sciences and Technology
Massachusetts Institute of Technology. Department of Biology
Massachusetts Institute of Technology. Department of Materials Science and Engineering
Massachusetts Institute of Technology. Engineering Systems Division
Terms of Use
Creative Commons Attribution
http://creativecommons.org/licenses/by/3.0/
Persistent DSpace Link
http://hdl.handle.net/1721.1/75741
DOI of Published Version
http://www.omicsonline.org/ArchiveJMBT/ArticleinpressJMBT.php
Repository logo
PrivacyPermissionsAccessibilityContact us
Repository logo
Notify us about copyright concerns.