November 21, 2008
| Bio-IT World > Pimp My Genome
Pimp My Genome


By Kevin Davies

Aug 15, 2005 | The first five albums by the British rock group Queen included a defiant footnote on the back cover, to wit: “No synthesizers were used in the making of this record.” It wasn’t until the ’80s that the band finally experimented with, or perhaps succumbed to, the inevitable march of technology.

DNA synthesizers, pioneered by Bio-IT World’s 2005 President Award winner Leroy Hood (see “Hood Hails ‘Century of Biology,’” page 19), have enjoyed a niche role in biotechnology at best for manufacturing DNA strands for microarray platforms and other applications. But as costs plummet, the ability to rapidly synthesize and customize longer, more intricate fragments of genomic DNA opens up a plethora of applications in basic and applied biology.

DNA synthesizersThe term “synthetic biology” was originally coined in 1980, but since 2003, its usage has become analogous to synthetic chemistry and covers the application of engineering and computer science to genomic circuits to construct small biological devices. As noted in a recent review*, these include “diagnostic tools that improve the care of patients with infectious diseases, as well as devices that oscillate, creep, and play tic-tac-toe.”

If there is a distinction, “synthetic genomics” is less about tinkering with genetic circuitry and more about customizing microbial vehicles “for groundbreaking scientific advances, including the development of alternative energy sources, and the production of new vaccines and pharmaceuticals,” says J. Craig Venter. “Synthetic genomics has the potential to enable significant societal, environmental, and medical benefits.”

This summer, two companies have established the beginning of a commercial synthetic biology industry. Codon Devices, founded by a quartet of molecular biologists from MIT, Harvard, and UC Berkeley, raised $13 million in venture capital (see “Synthetic Biologists Assemble Codon Devices Company,” July 2005 Bio-IT World, page 1). It will initially focus on developing customized genetic toolkits for biosensors and engineered cells for chemical and protein manufacture.

Meanwhile, Venter is stepping back into the boardroom (for the first time since leaving Celera Genomics in 2002) by founding Synthetic Genomics. Eschewing venture capital, the company has secured $30 million in private financing, about half from Mexican agrotechnology billionaire Alfonso Romo Garza. “We’re moving from reading the genetic code to writing it,” Venter told the Wall Street Journal, which broke the news of Venter’s new company. Having cracked the genome, evidently it’s time to start stitching it up again.

As if on cue, the J. Craig Venter Institute announced it will participate with MIT in a Sloan Foundation-funded project to examine the societal implications of synthetic genomics, particularly the potential risks and necessary safeguards to prevent bioterror abuses.

Minimal Genome
The significance of Venter’s arrival on the synthetic biology scene should not be underestimated, given his remarkable sixth sense for developing and exploiting key technologies. Venter’s first foray into synthetic genomics came six years ago with a landmark paper on the “minimal genome.” Although Japan’s Mitsuhiro Itaya first coined the term in 1995, Venter and colleagues published a landmark paper in Science in 1999 suggesting that a mere 300 genes might be necessary and sufficient to encode life. Progress was suspended while Venter tackled the human genome, but last year, his group took another important step with the “resynthesis” of a viral genome — an important proof-of-principle for synthetic genomics, which will require pimping much larger genomes.

The new Synthetic Genomics Web site says it all: “Imagine a future where clean, environmentally friendly microorganisms produce the bulk of industrial materials that are today made from petrochemicals...where specifically tailored organisms harness the sun to create clean energy...when researchers can use a modular, software-like product to design new microbial genomes which are manufactured on an industrial-like scale.”

This may sound a tad fanciful, but the tantalizing prospect of harnessing microbes to synthesize drugs and other biomaterials will not be lost on our readers. As for abundant clean energy, have you checked the price of oil lately?

______________________________

* Benner, S.A. and Sismour, A.M. “Synthetic biology.” Nat Rev Genet 6, 533-43; 2005.

Contact Kevin Davies at: kevin_davies@bio-itworld.com.

Click here to login and leave a comment.  

0 Comments

Add Comment

Text Only 2000 character limit

Page 1 of 1

White Papers & Special Reports

Waters white paper image
Software Helps Doping Control Lab Streamline Results Management
Sponsored by Waters
The Karolinska University Hospital’s Doping Control Lab tests thousands of samples annually for stimulants, diuretics, and other masking agents. Increased regulatory pressure and new technologies increased the number of samples analyzed creating data management challenges. Waters® NuGenesis® Scientific Data Management System and TargetLynx™ Application Manager software were used to reduce the time required to calculate, review and search results.


sas whitepaper92
Managed Innovation, Assured Compliance
Sponsored by SAS
Discovery organizations are identifying a lot of promising compounds, but clinical research processes haven't kept pace with timely testing of all those potential therapies. This white paper describes how SAS® Drug Development supports true innovation across the clinical trial process.

In this white paper you will learn how to:

  • Assemble data to foster better collaboration
  • Get up-to-date information during clinical trials
  • Make informed decisions earlier in the trial process


BlueArc white paper image
Addressing Life Sciences Constantly Growing Data Challenges Research Environments
Sponsored by BlueArc
The continued explosion of raw experimental data, the increased use of video, the growing adoption of new data retention practices, and the move to high throughput computational workflows are all placing new demands on the way life sciences organizations store and manage their data.

Download this white paper to learn about:

  • Factors driving the data explosion in the life sciences
  • New data management issues that must be addressed
  • HPC trends that are placing new demands on storage
  • Storage solution attributes that address performance, manageability, and energy efficiency.


Life Science Webcasts & Podcasts

Medidata Solutions

Rising Clinical Trial Delays and Costs - Addressing the Cause, Not the Symptoms 

medidata podcastProtocol complexity is taking a toll on clinical study speed and efficiency: increasingly complicated and ambitious protocols are not only burdening sites and study volunteers but are also prolonging trials and increasing expenses. In response, sponsors have turned to global study placement, restructured site relationships and new site management practices, but the problem remains.

This podcast will discuss:

  • Why these responses address only the symptoms, not the underlying cause, of rising clinical trial delays and costs.
  • Results of a recent joint Tufts University / Medidata Solutions study.
  • New metrics benchmarking protocol design trends.
  • Systematic protocol design improvements and why they are essential to clinical trial performance excellence.

Speakers: Ken Getz, Senior Research Fellow at the Tufts Center for the Study of Drug Development, and Ed Seguine, General Manager, Trial Planning Solutions at Medidata.

Download Now 



More Podcasts

Job Openings

Director, Center For Information Technology (CIT) - National Institutes of Health  (NIH), Department of Health and Human Service
Located in Bethesda, MD. This position requires:
• High-level vision, leadership, management, and modernization of CIT programs and services.
• Strategic direction and policy development for CIT long-term operations and objectives.
• Serve as a key IT advisor to the NIH Chief Information Officer.
A TOP SECRET security clearance will be required.  More job detail is found at:  http://www.jobs.nih.gov under the Executive Jobs section.Or contact Ms.Winnie Garner at seniorre@od.nih.gov.  Applications must be received ELECTRONICALLY by (11:59 p.m.), December 17, 2008.  DHHS and NIH are Equal Opportunity Employers

Bioinformatics Manager- Lilly Singapore Centre for Drug Discovery
For more information click here 

For reprints and/or copyright permission, please contact The YGS Group, 1808 Colonial Village Lane, Lancaster, PA;

(717) 399-1900 ext. 125, or via email to Ashley.Zander@theYGSgroup.com.