limited (see Table 6.5), and therefore harvesting of chemical energy from outside of the cell is
mandatory. For example, the E. coli cell contains up to 400 000 glucose molecules (Table 6.5) and each
glucose molecule can produce ~30 eV ~ 5 10
–18
J of energy (see Table 2.2.2 in Chapter 2). Thus,
based on Table 6.5, the total energy stored in cellular glucose in an E. coli cell is ~2 10
–12
J. Note that
in addition to glucose, energy is also stored in a number of derivatives of the glucose catabolism
process; therefore the total stored energy is somewhat larger, though it remains in the range estimated
above for glucose.
On the other hand, the power consumption of E. coli is about 1.4 10
–13
W(Table 6.5) and the cell
divides approximately every 2400 seconds (40 minutes – see footnote for Table 6.5). Thus the total
energy the cell uses during one division cycle is
E
cell
¼ 1:4 10
13
W 2400 s z 3 10
10
J (6.34)
When starving, E. coli consumes some of its ribosomes as an internal source of both energy and
nutrients (e.g. carbon and nitrogen) [43]. In fact, starvation of a population of E. coli cells results in
disintegration of some of the cells (lysis) within a few hours. Those cells that remain alive are then able
to utilize the remnant of dead bacteria to support their existence [44].
While at typical conditions occurring in nature E. coli does not have significant internal energy
storage, there are also exceptions. At some abnormal conditions E. coli can synthesize as much as 20%
of its dry weight as glycogen (glucose polymer) [54], which corresponds to ~10
–9
J of stored energy.
This amount of energy is equivalent to ~3x the cell cycle energy budget (6.34).
Many bacteria do not surv ive under long deprivation of nutrients. However, there can be
remar kable ex ceptions in whic h some bacteria have developed amazing mechan isms and optimi-
zation strategies to live under nutrient limitations [44–46]. Also cells can utilize other sources of
energy such as light as was briefly discussed in Chapter 1. Eukaryotic cells, on the other hand, which
are generally larger and more complex than bacte ria, can store a considerable amount of energy
internally.
6.10 BENCHMARK IN CARBO INFORMATION PROCESSOR
6.10.1 Top-down estimate of overall computational performance
As was discusse d above in Section 6.2.6, a conservative edge for estimated information content of
a bacterial cell such as E. coli is I
cell
~10
11
bits. In other words, for the correct placement of all
molecules within the cells, e.g. by the von Neumann’s universal constructor, 10
11
bits needs to be
generated by the cell processor. This quantity will be referred below as the binary information content
per task, I
task
¼ I
cell
, where ‘task’ refers to a completed assembly of a cell.
A measure of the information-processing rate can be made for the time required for a cell to
reproduce itself. A typical reproduction time of an E. coli cell is 2400 seconds (Table 6.5), and this is
taken to be time required for one computational task/cycle, t
task
. Thus the number of bits that must be
processed per second (bit rate), F
in carbo
, by the E. coli cell is:
F
incarbo
¼
I
task
t
task
w
10
11
2400
z 10
7
bit=s (6.35)
6.10 Benchmark in carbo information processor 177
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