With seed money from the National Science Foundation (NSF), SynBERC bioengineers from the University of California, Berkeley, and Stanford University are ramping up efforts to characterize the thousands of control elements critical to the engineering of microbes, so that eventually researchers can mix and match these "DNA parts" in synthetic organisms to produce new drugs, fuels or chemicals.

Today, a single designer microbe can take years to create and cost tens of millions of dollars, since each control element – a promoter or transcription factor has to be identified, characterized, and tweaked in order to be reused. One UC Berkeley project to engineer microbes to produce the anti-malarial drug artemisinin took 10 years to get out of the lab into small-scale production, at a cost of $25 million. The new BIOFAB: International Open Facility Advancing Biotechnology (BIOFAB), with two years of funding from NSF and matching support from founding partners, Lawrence Berkeley National Laboratory (LBNL) and the BioBricks Foundation (BBF), aims to produce thousands of free standardized DNA parts to shorten the development time and lower the cost of synthetic biology for academic or biotech laboratories.

“Synthetic biology has the potential to make the engineering of biology much easier and more affordable. Via the BIOFAB we will help ensure that the public’s investments and interests in the next generation of biotechnology return the greatest benefits,” said founding BIOFAB director Drew Endy, an assistant professor in Stanford’s Bioengineering Department and president of the BioBricks Foundation.

"This is an opportunity to build a framework that will allow us to set open standards for how we do biological design in the future, so that biological parts work reliably in everyone's hands," said BIOFAB co-director Adam Arkin, UC Berkeley professor of bioengineering and head of Synthetic Biology for LBNL’s Physical Biosciences Division.

BIOFAB takes its name from the fabrication, or Fab, service laboratories established in the early semiconductor industry to make it easier for academic and small industrial labs to design and manufacture small quantities of custom chips. With computer aided design (CAD) software, rapid-prototyping equipment and clean labs, Fab Labs could quickly produce innovative devices not yet ready for mass production.

“The professionally staffed BIOFAB production facility will provide an essential resource that will allow many academic researchers and others to rapidly prototype, test and translate their foundational discoveries and ideas into practice,” said Jay Keasling, UC Berkeley professor of chemical engineering and of bioengineering and senior faculty scientist and acting deputy director of LBNL. "By enabling everyone to better work together the BIOFAB will make the engineering of biology easier and more predictable." Keasling, who chairs the BIOFAB executive committee, led the project to biosynthesize artemisinin and is now director of the Department of Energy's Joint BioEnergy Institute (JBEI) in Emeryville, which focuses on developing commercially viable biofuels.

Endy and Arkin proposed a similar Fab Lab for biology more than 10 years ago, but only now, Endy said, is the time ripe for an open and cooperative full-scale production facility. "Besides Tom Knight [of the Massachusetts Institute of Technology], very few people were talking about standard biological parts 10 years ago," he said, while today, such parts are widely used by college students as part of the International Genetically Engineered Machine competition (iGEM), catalogued by institutions such as the Massachusetts Institute of Technology and JBEI, and used daily in synthetic biology labs around the world. Nevertheless, of the estimated 3,500 critical control elements in an E. coli bacterium, fewer than 100 have been seriously studied and characterized. Of the 500-plus promoters listed in current registries, for example, fewer than 50 have been measured, Endy said.

"What exists today is not a professional parts catalog," Arkin said. "But the parts we have, while not perfect, are better than nothing, and they are helping researchers all over the world."

"We now need to move beyond Lego™ metaphors and genetic toys to professional technologies,” Endy added.

Operating in partnership with the Synthetic Biology Engineering Research Center (SynBERC), directed by Keasling, BIOFAB is raising additional funds to hire 29 full-time staff who will systematically refine, standardize and characterize the activity of each genetic control element in E. coli, so that large-scale collections of genetic parts can be treated more like standardized components. What the researchers learn will be applied to parts collections in other microbes and used to assemble engineered biological systems.

"Even though we will be building parts and making systems, we are still in the foundational research stage," Arkin cautioned. "But in starting BIOFAB, we will accumulate the specialized know-how and the community of researchers necessary to become a resource for production and training in synthetic biology." BIOFAB also will promulgate standards for technical and professional practice through application of resources such as the BioBrick Public Agreement, a new legal framework supporting open technology platforms in genetic engineering.

To best accomplish its goals, the BIOFAB is also fully integrating ethics research within its production planning and operations. “Our task is to generate resources and help make decisions regarding ethical issues, including safety, security and communities in genetic engineering, so that we can lead the development of open technology platforms in biotechnology that increase capacities and support human flourishing,” noted Gaymon Bennett, Doctor of Theology and head of BIOFAB Human Practices.

More information and announcements of open positions is available via http://www.biofab.org/