Team:BostonU

Synthetic biology exists more as a form of art than a reproducible, well-defined production chain. From laboratory to laboratory, the experiments vary in procedure, characterization, and yield. The main product of synthetic biology— engineered organisms, are available only to the highly-experienced researcher and are not without the costs of timely preparation and low product yield. Consequently, the lack of standardization across the field has impeded the product from ever reaching a wide industry audience. More recent engineering efforts in the assembly of gene circuits has provided a pathway to a modular view of genetic parts. Termed the Modular Cloning Assembly Method (MoClo), this novel single-pot reaction protocol is a time-effiecient, two-enzyme system for DNA assembly.  (Weber et al., 2011). Before MoClo can reach its full potential across research and industry interests, the synthetic biology community needs a standardized and well-characterized library of MoClo parts for Escherichia coli to enable protocol automation and informed device designing. The 2013 Boston University iGEM Team seeks to bridge this gap in the product development chain by building such a standard library and characterizing the parts through flow cytometry. To further efforts to develop automated design for synthetic biology, we will be doing the following:

• preparing protocols for a TECAN liquid-handling robot
• providing feedback on Clotho 2.0 software tools including the EugeneCAD language to a team of developers in the CIDAR
• Working with BBN Technologies's TASBE Data Analysis Program.

Furthermore, we are working with the Wellesley Desyne team to develop an easy-to-use visualized programming language to wrap around Eugene. Lastly, we are expanding the 2012 BostonU iGEM team's work on a Data Sheet web application to generate standardized part information and sharing with the help of the Purdue Biomaker's iGEM Team.