عنوان

BglBrick vectors and datasheets:

Number

LA99x1j98w

Title Proper

BglBrick vectors and datasheets:

General Material Designation

[Article]

First Statement of Responsibility

Lee, Taek Soon; Krupa, Rachel A; Zhang, Fuzhong; Hajimorad, Meghdad; Holtz, William J; Prasad, Nilu; Lee, Sung Kuk; Keasling, Jay D

Title Proper by Another Author

A synthetic biology platform for gene expression.

Text of Note

As engineered biological systems become more complex, it is increasingly common to express multiple operons from different plasmids and inducible expression systems within a single host cell. Optimizing such systems often requires screening combinations of origins of replication, expression systems, and antibiotic markers. This procedure is hampered by a lack of quantitative data on how these components behave when more than one origin of replication or expression system are used simultaneously. Additionally, this process can be time consuming as it often requires the creation of new vectors or cloning into existing but disparate vectors.Here, we report the development and characterization of a library of expression vectors compatible with the BglBrick standard (BBF RFC 21). We have designed and constructed 96 BglBrick-compatible plasmids with a combination of replication origins, antibiotic resistance genes, and inducible promoters. These plasmids were characterized over a range of inducer concentrations, in the presence of non-cognate inducer molecules, and with several growth media, and their characteristics were documented in a standard format datasheet. A three plasmid system was used to investigate the impact of multiple origins of replication on plasmid copy number.The standardized collection of vectors presented here allows the user to rapidly construct and test the expression of genes with various combinations of promoter strength, inducible expression system, copy number, and antibiotic resistance. The quantitative datasheets created for these vectors will increase the predictability of gene expression, especially when multiple plasmids and inducers are utilized.

Date of Publication

2011

Title

Lawrence Berkeley National Laboratory

Electronic name

[Article]

275578

a

Y