Difference between revisions of "Part:BBa K861140"
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+ | ===Characterized by XJTU-China 2020=== | ||
+ | We cloned and confirmed the target fragment by PCR. The length of our fragment is 981bp. The following results showed the successful result. | ||
+ | <div>[[File:T--XJTU-China--Eggel.png |700px|thumb|center|<b>Figure 1:</b>PCR confirmation of the target fragment.]]</div> | ||
+ | <div>[[File:T--XJTU-China--Bgimprove02.jpeg |700px|thumb|center|]]</div> | ||
+ | <div>[[File:T--XJTU-China--Bgimprove01.jpeg |700px|thumb|center|]]</div> | ||
+ | the mRNA level of B.s GalU is ~2.4 fold higher than that of E.coli, indicating the significant improvement of enzyme expression and activity. However, due to the lower expression of another key enzyme PGM for EPS production in BE strain, the final EPS yield is lower than that of EE strain but still comparable. | ||
<!-- Add more about the biology of this part here | <!-- Add more about the biology of this part here | ||
===Usage and Biology=== | ===Usage and Biology=== |
Revision as of 03:43, 28 October 2020
GalU,glucose-1-phosphate uridylyltransferase
UTP-glucose-1-phosphate uridylyltransferase (GalU) carries out a key step in the generation of UDP-D-glucuronate.GalU catalyzes the addition of UTP to α-D-glucose 1-phosphate to yield UDP-D-glucose,which is the substrate for cellulose synthetase complex to produce cellulose.
Characterized by XJTU-China 2020
We cloned and confirmed the target fragment by PCR. The length of our fragment is 981bp. The following results showed the successful result.
the mRNA level of B.s GalU is ~2.4 fold higher than that of E.coli, indicating the significant improvement of enzyme expression and activity. However, due to the lower expression of another key enzyme PGM for EPS production in BE strain, the final EPS yield is lower than that of EE strain but still comparable. Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal NgoMIV site found at 69
Illegal AgeI site found at 387
Illegal AgeI site found at 510 - 1000INCOMPATIBLE WITH RFC[1000]Illegal SapI.rc site found at 783