[BBF Standards] BioHackathon, or Characterization Challenge
Drew Endy
endy at MIT.EDU
Mon Feb 11 21:48:25 EST 2008
First, let me point out to the list who's versus whose:
http://www.wsu.edu/~brians/errors/who's.html
Meanwhile, Bryan, your comment might be well connected to something I
was struggling to say...
On Feb 11, 2008, at 9:35 PM, Bryan Bishop wrote:
> I would like to point out to the list that doubling rate is strongly
> linked to development cycle time in terms of biobricks and the
> standards. It seems to be nearly equivalent to waiting for the
> compiler
> to finish (except, biobricks are like precompiled bytecode).
As soon as we start working with doubling times below 40 minutes, for
many of our systems, the debugging time constant for system
performance is limited not by cell growth rate, but rather by the time
it takes for protein (and other molecular) levels to rise and fall.
Some of the fastest protein production systems around are found in
phage, the best of which can produce convert most of E.coli into phage
specific proteins by 10-20 minutes post infection. Faster than this
and we have to start thinking carefully about how cell doubling time
is driving the reset of system state to ground.
Meanwhile, note that we should be able to deploy active mRNA and
protein degradation systems (e.g., ClpX) to push faster reset times
independent of the cell growth rate (c/o Bob Sauer et al.).
So, eventually, my guess would be that we want to consider cell
doubling times for specific purposes (i.e., production of DNA, cells,
or other objects), but otherwise figure out how to decouple the
operation of our engineered biological systems from cell doubling time.
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