Difference between revisions of "Team:UESTC-China/Design"

How to integrate the two related pathways which is involved in the straw degradation and the synthesis of butanol and hydrogen? According to previous studies, we designed three module vectors in the present work. The first module piGEM2018-Module001 is designed to achieve the transform from straw to glucose, and it performed the function of bifunctional enzyme. The other two modules piGEM2018-Module002 and piGEM2018-Module003 were designed to produce two types of clean energy, butanol and hydrogen from glucose (Fig. 1). After we checked if these three modules could work independently, we aimed to combine them together to achieve efficient conversion of straw to butanol and hydrogen in the near future.

There are three modules synthesized in our energy conversion systems, including straw degradation, butanol production and hydrogen production (Fig. 2 ). Prior to the DNA synthesis, we carried out the codon optimization for the purpose to gain better expression for the target genes in E. coli.

As shown in Fig. 2, the structure of straw is compact and is difficult to be decomposed, because cellulose is wrapped by hemicellulose, and is interspersed with lignin via ferulate ester bond (Fig. 3 ). It has been found that the presence of lignin would give rise to the reduced cellulase activity. Therefore, it is necessary and significant to pretreat the straw to make it separate with the lignin. The commonly used methods included physical method, chemical method and biological method. The physical method is not suitable for the industrial production because of its complication and high cost. Chemical methods often cause environmental pollution due to the usage of large amount of acid or alkali. Biological method has been unable to treat straw directly because of its low enzyme activity with the presence of lignin. Nevertheless, we know from some literatures that ferulic acid esterase, xylanase and β-glucosidase have synergistic effect, which greatly accelerated the degradation rate of straw [1].

The enzymes Xyn10D-fae1A, Xyl3A, Cex and CenA are the key enzymes to degrade straw into glucose and other products shown in Fig. 4a. Xyn10D-fae1A is the bifunctional enzyme, which has the activity of both ferulic acid esterase and xylanase. Ferulic acid esterase (abbreviated as fae1A) can break the ferulic acid ester bond, which is responsible for attaching the complex cellular cell wall structures. Xylanase can hydrolyze xylan existing in plant cell wall, in which it can cut the β-1,4 glycosidic bond between the xylose residues in the xylan backbone [2]. From BioBrick, we found the endoglucanase CenA, (BBa_K118023) and exoglucanase Cex, (BBa_K118022). Cellulose will be degraded into glucose with the help of Xyl3A, CenA and Cex [3]. Besides, an extra signal peptide pelB followed by five aspartate repeats (pelB+5D seen in Fig. 4b) were introduced to facilitate the extracellular expression of the four enzymes in E. coli [4].

In order to meet the needs of industrial production of butanol, a butanol synthesis pathway existed in native Clostridium was rebuilt in E. coli. According to literature which studies the screening of the same enzymes of different species, we finally tried to assemble a relatively superior combination [5], which mainly uses six genes to construct a biosynthetic pathway from glucose to butanol (Fig. 5a).

FRE_adhE and FRE_ackA is the upstream of AdhE and AckA gene, which includes the promoter, ribosome binding site (RBS) and the entire transcription factor (TF) binding site. They has been adopted by Wen et al. to enhance the production of butanol in E. coli without adding revulsant, antibiotics and under anaerobic fermentation conditions, which is hard for industrial production [6]. We want to not only produce large amounts of butanol, but also meet the needs of lower cost production. Therefore, We assemble these parts together and construct our plasmid of butanol production (Fig. 5b).

The accumulation of butanol exerts a greatly inhibitory effect on cell growth during butanol production process. Thus, we will import GroESL gene from Clostridium acetobutylicum to allow E. coli expresses heat shock protein groESL chaperone, which has shown the function for improving the yield of butanol by [7] (Fig. 5c).

E. coli is a microorganism capable of producing hydrogen under anaerobic conditions, which can convert the methyl formate to hydrogen gas and carbon dioxide (Fig. 6a) via an enzyme complex called formate hydrogenlyase (FHL) [8]. It has been reported that FhlA, an activating protein of FHL, could enhance the production capacity of hydrogen [8]. Additionally, structural analysis showed that FHL from E. coli belongs to [Ni-Fe] hydrogenase family. Its enzymatic activity is about 100 times lower than another hydrogenase from green algae and some bacteria. Therefore we introduced the gene encoding the hydrogenase from Enterobacter cloacae IIT-BT 08 into E. coli to further increase hydrogen production [9] (Fig. 6b).

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