Difference between revisions of "Team:HUST-China/Description"

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Revision as of 14:24, 12 October 2018

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Discription

Shewanella

In the part of Shewanella, we employ Shewanella oneidensis MR-1 as our chassis and pyydt as the plasmid. Shewanella could utilize the lactate as its carbon source and produce electricity with the help of a multiprotein porin-cytochrome complex on its outer membrane called MtrABC. MtrABC could transfer the electron from Shewanella’s inner membrane to the surrounding. pYYDT is a shuttle plasmid between E.Coli and Shewanella. We constructed this plasmid in E.Coli and transferred it into Shewanella by conjugating these two kinds of bacteria.

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Our design of constructing Shewanella is devided into two parts: improvement of utilization of lactate and increment of the amount of NADH in Shewanella.

(1). Improvement of utilization of lactate: To make the use of lactate more efficiently, we overexpress four genes: dld-Ⅱ, lldE, lldF, lldG.

①. dld-Ⅱ: dld-Ⅱ refers to FAD-dependent D-lactate dehydrogenase which could catalyze D-lactate’s transformation into pyruvate.

②. lldE/lldF/lldG: They could encode a L-lactate dehydrogenase complex which could catalyze D-lactate’s transformation into pyruvate.

We constructed them separately in pYYDT and found out if there was any improvement at the amount of electricty produced by our Shewanella.

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Then we put these four genes in one circuit to level up the production of electricity.

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(2). Increment of the amount of NADH in Shewanella

To achieve this goal, we overexpress these four genes: gapA2, mdh, pflB, fdh*. We chose them according to our reference.

①. gapA2: It encodes glyceraldehyde-3-phosphate dehydrogenase which could transform 3- phosphoglyceraldehyde into 1,3- diphosphoglycerate

②. mdh: It encodes NAD dependent malate dehydrogenase which transforms malate into pyruvate

③. pflB: It encodes pyruvate formate-lyase to transform pyruvate into Acetyl-CoA

③. pflB: It encodes pyruvate formate-lyase to transform pyruvate into Acetyl-CoA

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According to our model, we divided these four genes into two groups: gapA2/mdh and pflB/fdh*.

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Finally, we put all these genes into one circuit and found out if the amount of electricity could reach the maximum.

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