Difference between revisions of "Part:BBa K2262015"
Line 32: | Line 32: | ||
<br> | <br> | ||
<br> | <br> | ||
− | [[File:Agarose gel SP.png| | + | [[File:Agarose gel SP.png|800px|thumb|center|'''Figure 3.''' The electrophoresis of BBa_J23119 and BBa_J23109. ]] |
<br> | <br> | ||
<br> | <br> | ||
Line 48: | Line 48: | ||
<br> | <br> | ||
<br> | <br> | ||
+ | | ||
+ | The results showed that the growth of E.coli DH5Alpha won’t be affected by the arsenic concentration below 100ppm.(Table 2) | ||
+ | [[File:FMt table2.png|600px|thumb|center|'''Table 2.'''The growth of E.coli DH5Alpha in different conditions. ]] | ||
+ | <br> | ||
+ | <br> | ||
+ | |||
<!-- 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 22:42, 31 October 2017
Constitutive Promoter + RBS + fMt
Introduction
This sequence is designed for constitutively chelating arsenic ions. We ligated a constitutive promoter(BBa_J23119) with metallothionein (fMT, BBa_K190019) to produce arsenic-binding protein. This metallothionein (fMT) is a kind of chelating protein from Fucus vesiculosus. It can bind both Arsenite (III) and Arsenate(V). This part was first designed by Groningen of iGEM 2009. The part of K190019 consists of fMT and RBS(ribosome--‐binding Site, for initiating translation).
Modifying and Improving the Existed Biobrick
Previous biobrick BBa_K190031 of 2009 iGEM10_Groningen
The metallothionein (BBa_K190031) is a fMT(BBa_K190019) under control of a low constitutive promotor (BBa_J23109). We failed several times in replicating the ligation of these two parts. After sequencing BBa_K190031, BBa_K190019, and BBa_J23109, we found the constitutive promoter BBa_J23109 has two Spel restriction sites in the prefix.(Figure 2.) Thus, we decided to modify the biobrick by ligating fMT(BBa_K190019) with another constitutive promoter (BBa_J23119). The Figure 3 shows the electrophoresis of BBa_K190019 when its plasmid was cut by Xba I and Pst I. And the Figure 4 shows the electrophoresis of BBa_J23119 and BBa_J23109 when their plasmids were cut by Spe I and Pst I.
Result
1. Fungal Test
We first examined the growth curve of E. coli DH5Alpha in arsenic solution. We compared the growth curve of E. coli DH5 in arsenic solution with that curve in solution without arsenic ions. The Table 1 shows the experiment design for the growth curve of E. coli DH5Alpha.
The results showed that the growth of E.coli DH5Alpha won’t be affected by the arsenic concentration below 100ppm.(Table 2)
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 7
Illegal NheI site found at 30 - 21INCOMPATIBLE WITH RFC[21]Illegal BglII site found at 81
- 23COMPATIBLE WITH RFC[23]
- 25INCOMPATIBLE WITH RFC[25]Illegal NgoMIV site found at 170
- 1000COMPATIBLE WITH RFC[1000]