TY - JOUR
T1 - Tuning the Catalytic Activity of Subcellular Nanoreactors
AU - Jakobson, Christopher M.
AU - Chen, Yiqun
AU - Slininger, Marilyn F.
AU - Valdivia, Elias
AU - Kim, Edward Y.
AU - Tullman-Ercek, Danielle
N1 - Funding Information:
This work was supported by the National Science Foundation (award MCB1150567 to D.T.-E.), the Army Research Office (grant W911NF-15-1-0144 to D.T.-E.), a Knowledge Build grant from ExxonMobil Corporation (to D.T.-E.), a UC Berkeley Fellowship (C.M.J.), the UC Berkeley Undergraduate Research Apprenticeship Program (Y.C.), and the NIH Bridges to Baccalaureate Program (E.V.).
PY - 2016/7/31
Y1 - 2016/7/31
N2 - Bacterial microcompartments are naturally occurring subcellular organelles of bacteria and serve as a promising scaffold for the organization of heterologous biosynthetic pathways. A critical element in the design of custom biosynthetic organelles is quantitative control over the loading of heterologous enzymes to the interior of the organelles. We demonstrate that the loading of heterologous proteins to the 1,2-propanediol utilization microcompartment of Salmonella enterica can be controlled using two strategies: by modulating the transcriptional activation of the microcompartment container and by coordinating the expression of the microcompartment container and the heterologous cargo. These strategies allow general control over the loading of heterologous proteins localized by two different N-terminal targeting peptides and represent an important step toward tuning the catalytic activity of bacterial microcompartments for increased biosynthetic productivity.
AB - Bacterial microcompartments are naturally occurring subcellular organelles of bacteria and serve as a promising scaffold for the organization of heterologous biosynthetic pathways. A critical element in the design of custom biosynthetic organelles is quantitative control over the loading of heterologous enzymes to the interior of the organelles. We demonstrate that the loading of heterologous proteins to the 1,2-propanediol utilization microcompartment of Salmonella enterica can be controlled using two strategies: by modulating the transcriptional activation of the microcompartment container and by coordinating the expression of the microcompartment container and the heterologous cargo. These strategies allow general control over the loading of heterologous proteins localized by two different N-terminal targeting peptides and represent an important step toward tuning the catalytic activity of bacterial microcompartments for increased biosynthetic productivity.
KW - 1,2-propanediol utilization
KW - Salmonella
KW - bacterial microcompartments
KW - subcellular organelles
KW - synthetic biology
UR - http://www.scopus.com/inward/record.url?scp=84979944281&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84979944281&partnerID=8YFLogxK
U2 - 10.1016/j.jmb.2016.07.006
DO - 10.1016/j.jmb.2016.07.006
M3 - Article
C2 - 27427532
AN - SCOPUS:84979944281
SN - 0022-2836
VL - 428
SP - 2989
EP - 2996
JO - Journal of Molecular Biology
JF - Journal of Molecular Biology
IS - 15
ER -