Optimization

To maximize the isobutanol production, we optimize E.coli strains, culture medium, time, temperature and carbon source. Amazingly, our production surpasses the published reference whose production is 6.8g/L for 24 hr by using modified JCL16 strain（Smith KM, Liao JC, An evolutionary strategy for isobutanol production strain development in Escherichia coli,2011.）.

　Medium optimization

First, we tried to find the most suitable medium for DH5α to produce isobutanol.

We cultured the DH5α strain in the common medium, M9,M9T(M9+ trace metal mix) and M9TY(M9+ trace metal mix+ yeast extract) in the low temperature release system. Data shows that when we changed M9 into M9T medium, the yield increased 10 times from 0.05% to 0.5%. Furthermore, when changed M9T into M9TY, the yield increased more than 50% from 0.5% to 0.8%! Consequently, M9TY is the most appropriate medium. And, this medium conforms to the journal we refers to（Smith KM, Liao JC, An evolutionary strategy for isobutanol production strain development in Escherichia coli,2011.）, so we decided to use M9TY as our medium in our upcoming experiments.

　E.coli strain optimization

Next, we wanted to know that if other strains could have great productivity of isobutanol. So, we tested the following five strains: DH5α,DH10b,JM109,MG1655,EPI300.

According to the result (Figure 18.), we knew that DH5α produced the most isobutanol. So, we choose DH5α to produce isobutanol on our upcoming experiments.

　How do we change our culture conditions?

After activating overnight in 37℃,we transferred 1/100 of volume to the new medium then cultured in 37℃ until OD₆₀₀ reached 0.2, we set this point as 0 hour and transferred each tube to different condition at specific time. (Figure 19.)

　Culture time and temperature optimization

After knowing the most appropriate medium and strain, we tried to find out the best condition, including temperature and culture time, for our host cell to produce isobutanol.

The report indicates that changing from 37℃ environment into lower temperature environment did produce more isobutanol. (Figure 20.) We could see that E.coli being in 37℃ environment for 20 hours and in 32℃ environment for 4 hours have the highest production quantity of isobutanol.

According to the data (Figure 21.), we discovered that E.coli under 42℃ environment for 24 hours would have higher production of isobutanol than under 37℃ environment at the beginning. This result is totally out of our expectation, and the high production really surprised us! There are several factors that influence the production rate of isobutanol as follows:

(1) Concentration of enzymes

A higher concentration of enzymes leads to more effective collisions per unit time, which leads to an increasing reaction rate. However, the higher protein expression level is a metabolic load of host cells and decrease the growth rate.

(2) Temperature

Usually, an increase in temperature is accompanied by an increase in the reaction rate. Temperature is a measure of the kinetic energy of a system, so higher temperature implies higher average kinetic energy of molecules and more collisions per unit time. But the enzyme has its suitable reaction temperature, higher temperature may decrease the enzyme activity.

(3) Presence of the byproducts

he α-ketoisovalerate decarboxylase (Kivd) is a unique lactococcal key enzyme in the decarboxylation of branched-chain α-keto acids derived from branched-chain amino acids transamination into aldehydes. The promiscuous nature of kivd decarboxylase does not allow good selectivity in the decarboxylation step. Intermediate byproducts such as isobutyrate were present in the fermentation broth. The byproducts decreas the production rate of isobutanol.

Because of these factors affect the final isobutanol concentration,many versions of synthetic circuits which have different protein expression levels are needed to created to test performance in reliability and consistency, but this process is both tedious and time consuming. To overcome this problem, we develop a temperature control method to construct a isobutanol production circuit that can use culture temperature shifts to control the expression levels of a series of metabolic proteins at the precise times. The experimental data in Fig. 7 reveal the design method works successfully, and E.coli under 42℃ environment for 24 hours have higher production of isobutanol (~0.75%).

　Carbon source optimization

Knowing that glycerol is the redundant product of the petroleum pyrolysis, we wanted to reduce the useless byproduct of petroleum Industry on earth. We fed our host with glycerol to see whether it is possible to be our E.coli‘s carbon source or not.

We discovered that using glycerol as carbon source could get the 1/3 of the yield of isobutanol produced by using glucose as carbon source. In this result (Figure 22.), the industrial byproduct, glycerol, can also be digested by our host and turned into the promising bio-fuel.

Furthermore, we also compared the productivity of different temperature.

By comparing 37℃ & 30℃ to 42℃, we found out that the best temperature to produce isobutanol is 42℃. From this figure, the productivity of all temperature decreased obviously after 24 hours. Thus, we conjectured that the isobutanol effused out to the air or the intermediate products of isobutanol pathway were converted into other byproducts.