TY - JOUR
T1 - Spanning high-dimensional expression space using ribosome-binding site combinatorics
AU - Zelcbuch, Lior
AU - Antonovsky, Niv
AU - Bar-Even, Arren
AU - Levin-Karp, Ayelet
AU - Barenholz, Uri
AU - Dayagi, Michal
AU - Liebermeister, Wolfram
AU - Flamholz, Avi
AU - Noor, Elad
AU - Amram, Shira
AU - Brandis, Alexander
AU - Bareia, Tasneem
AU - Yofe, Ido
AU - Jubran, Halim
AU - Milo, Ron
N1 - Funding Information:
European research council [260392—SYMPAC]; The Leona M. and Harry B. Helmsley Charitable Trust; Israel Science Foundation [750/09]; Anna and Maurice Boukstein career development chair (to R.M.); Azrieli Foundation award and an Azrieli Fellowship (to E.N.). Funding for open access charge: European Research Council [260392—SYMPAC]; Israel Science Foundation [750/09].
PY - 2013/5
Y1 - 2013/5
N2 - Protein levels are a dominant factor shaping natural and synthetic biological systems. Although proper functioning of metabolic pathways relies on precise control of enzyme levels, the experimental ability to balance the levels of many genes in parallel is a major outstanding challenge. Here, we introduce a rapid and modular method to span the expression space of several proteins in parallel. By combinatorially pairing genes with a compact set of ribosome-binding sites, we modulate protein abundance by several orders of magnitude. We demonstrate our strategy by using a synthetic operon containing fluorescent proteins to span a 3D color space. Using the same approach, we modulate a recombinant carotenoid biosynthesis pathway in Escherichia coli to reveal a diversity of phenotypes, each characterized by a distinct carotenoid accumulation profile. In a single combinatorial assembly, we achieve a yield of the industrially valuable compound astaxanthin 4-fold higher than previously reported. The methodology presented here provides an efficient tool for exploring a high-dimensional expression space to locate desirable phenotypes.
AB - Protein levels are a dominant factor shaping natural and synthetic biological systems. Although proper functioning of metabolic pathways relies on precise control of enzyme levels, the experimental ability to balance the levels of many genes in parallel is a major outstanding challenge. Here, we introduce a rapid and modular method to span the expression space of several proteins in parallel. By combinatorially pairing genes with a compact set of ribosome-binding sites, we modulate protein abundance by several orders of magnitude. We demonstrate our strategy by using a synthetic operon containing fluorescent proteins to span a 3D color space. Using the same approach, we modulate a recombinant carotenoid biosynthesis pathway in Escherichia coli to reveal a diversity of phenotypes, each characterized by a distinct carotenoid accumulation profile. In a single combinatorial assembly, we achieve a yield of the industrially valuable compound astaxanthin 4-fold higher than previously reported. The methodology presented here provides an efficient tool for exploring a high-dimensional expression space to locate desirable phenotypes.
UR - http://www.scopus.com/inward/record.url?scp=84877292750&partnerID=8YFLogxK
U2 - 10.1093/nar/gkt151
DO - 10.1093/nar/gkt151
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C2 - 23470993
AN - SCOPUS:84877292750
SN - 0305-1048
VL - 41
SP - e98
JO - Nucleic Acids Research
JF - Nucleic Acids Research
IS - 9
ER -