Synthetic Biology Parts, Devices and Applications

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86 5 Functional Requirements in the Program and the Cell Chassis for Next-Generation Synthetic Biology


worn‐out components. The relationship between the machine and the program
is central to this essential interaction. This situation is also common in contem­
porary computers, which remember our past actions and do not behave today as
they did some time ago, improving their adaptation to our wishes as time elapses.
In cells, this corresponds to exploiting an information that is not directly present
in the genes, but, rather, to a contextual information present in the way genes are
placed (and sometimes tagged by specific biochemical processes) in the genome
and its disposition within the cell as well as in the ultimate matter making the
genome. We note in passing that the transplantation founding experiments tells
us something more in terms of functions. It uncovers the first hidden functional
constraint on the genome structure: the chromosome needs to be compacted to
fit a small volume, and this is why (Figure 5.2) the transplantation experiment
requires as a first step the making of a syncytium to accommodate a decondensed
DNA molecule [27].

5.4 Helper Functions


For life to keep going and to develop into a descent, a chore of helper functions
is needed. These functions operate at different levels. They are organized along
hierarchies that are segmented (like organs in an animal body) or branched

Mycoplasma capricolum Mycoplasma mycoides

Final chassis = donor’s

Receiving chassis

Chassis of the donor

Replication

Reproduction

Chromosome of the host Chromosome of the donor

Tr ansplant

ation

PEG fusion

Transplanted DNA
condensation

Host DNA
degradation

DNA decondensation

Tr ansplanted DNA-
directed growth

Cell lysis

Chassis of the host

Figure 5.2 Replication of the program, reproduction of the chassis. The sequence of the
ycoplasma mycoides DNA transplanted into ycoplasma capricolum is identical to that at the
end of the experiment. Transplantation has triggered degradation of the. capricolum
DNA, while the DNA of. mycoides replicates and dilutes out the component of the initial
host. At the end of the experiment, the components of the cells are identical to those of

. mycoides, not to those of the recipient. capricolum.

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