Difference between revisions of "Part:BBa K2963033"

Revision as of 11:30, 20 October 2019

Ptac(two lacOs)-racE- Producing γ-PGA with different D/L monomer ratio

Our project used this part to produce γ-PGA with different D/L glutamate monomer ratios.This part contains the racE gene, which was under the control of a modified tac promoter with another additional operator gene (lacO). We used racemase activity data and real-time PCR data to characterize and compare the different expression intensities of racE gene using different structures of tac promoters.

Usage and Biology

The racE gene is derived from Bacillus subtilis. This gene encodes a racemase which can converts L-glutamic acid to D-glutamate.

Characterization

We used real-time quantitative PCR and enzyme activity assay to compare the different expressions of racE gene under the control of tac promoter containing different numbers of operator genes in Corynebacterium glutamicum. The results were shown in Figure 1. The expression level of the racE gene at 8 h, 16 h, 24 h decreased by 29.99%, 58.86% and 62.34% respectively. The results showed that the expression intensity of racE was effectively reduced at each transcriptional stage by the tandem of two lacOs compared to one lacO. At the same time, we tested the activity of the racemase in cells. The enzyme activity under the control of one lacO is higher than that with two lacOs. The data is shown in Figure 2.

Figure1

Figure 1. The expression level of the racemase gene racE at 8 h, 16 h, 24 h decreased by 29.99%, 58.86% and 62.34% respectively. The results show that the expression intensity of racE was effectively reduced at each transcriptional stage by the tandem of two lacOs compared to one lacO.

Figure2

Figure 2. we tested the enzyme activity of the racemase in cells. The enzyme activity under the control of one lacO is higher than that with two lacOs.

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 <partinfo>BBa_K2963033 short</partinfo>
-Our project used this part and part （BBa_K2963032）to produce γ-PGA with different D/L glutamate monomer ratios.This part contains the racE racemase gene, which was constructed using a modified tac promoter (BBa_K2963030) with another additional operator gene (lacI), rbs (BBa_K2963006), racE gene (BBa_K2963004) and the T7 terminator (BBa_K2598024). The parts BBa_K2963030, BBa_K2963006, BBa_K2598024 are contained in the ePathBrick loop vector pZM1 (Ptac) containing the inducible tac promoter. This part is compared with part (BBa_K2963032) and we used racemase activity data and real-time PCR data to characterize these two composite parts and compare the different expression intensities of racE gene using different structures of tac promoters.
+Our project used this part to produce γ-PGA with different D/L glutamate monomer ratios.This part contains the <i>racE</i> gene, which was under the control of a modified tac promoter with another additional operator gene (<i>lacO</i>). We used racemase activity data and real-time PCR data to characterize and compare the different expression intensities of <i>racE</i> gene using different structures of tac promoters.
 ===Usage and Biology===
-The racE gene is derived from Bacillus subtilis. This gene encodes a racemase which can converts L-glutamic acid to D-glutamate.
+The <i>racE</i> gene is derived from <i>Bacillus subtilis</i>. This gene encodes a racemase which can converts L-glutamic acid to D-glutamate.
 ===Characterization===
-We used real-time quantitative PCR and enzyme activity assay to compare the different expressions of racE gene under the control of tac promoter containing different numbers of operator genes in Corynebacterium glutamicum.
+We used real-time quantitative PCR and enzyme activity assay to compare the different expressions of racE gene under the control of tac promoter containing different numbers of operator genes in <i>Corynebacterium glutamicum</i>.
-The results were shown in Figure 1. The expression level of the racE gene at 8 h, 16 h, 24 h decreased by 29.99%, 58.86% and 62.34% respectively. The results showed that the expression intensity of racE was effectively reduced at each transcriptional stage by the tandem of two lacOs compared to one lacO. At the same time, we tested the enzyme activity of the racemase in cells. The result was the same as the above and the enzyme activity was different. The data is shown in Figure 2.
+The results were shown in Figure 1. The expression level of the <i>racE</i> gene at 8 h, 16 h, 24 h decreased by 29.99%, 58.86% and 62.34% respectively. The results showed that the expression intensity of <i>racE</i> was effectively reduced at each transcriptional stage by the tandem of two <i>lacOs</i> compared to one <i>lacO</i>. At the same time, we tested the activity of the racemase in cells. The enzyme activity under the control of one <i>lacO</i> is higher than that with two <i>lacO</i>s. The data is shown in Figure 2.
+Figure1
 [[image:Figure1-gaohaixin.png|400px]]
-Figure 1. The expression level of the racemase gene racE at 8 h, 16 h, 24 h decreased by 29.99%, 58.86% and 62.34% respectively. The results show that the expression intensity of racE was effectively reduced at each transcriptional stage by the tandem of two lacOs compared to one lacO.
+Figure 1. The expression level of the racemase gene racE at 8 h, 16 h, 24 h decreased by 29.99%, 58.86% and 62.34% respectively. The results show that the expression intensity of <i>racE</i> was effectively reduced at each transcriptional stage by the tandem of two <i>lacO</i>s compared to one <i>lacO</i>.
+Figure2
 [[image:Figure2-gaohaixin.png|400px]]
-Figure 2. we tested the enzyme activity of the racemase in cells. The result was the same as the above and the enzyme activity was different.
+Figure 2. we tested the enzyme activity of the racemase in cells. The enzyme activity under the control of one <i>lacO</i> is higher than that with two <i>lacO</i>s.
 <!-- Add more about the biology of is part here.