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BL21(DE3) strain using alkyl sulfatase protein (SdsA1) derived from Pseudomonas sp. | BL21(DE3) strain using alkyl sulfatase protein (SdsA1) derived from Pseudomonas sp. | ||
ATCC 19151 where it is has been shown to be responsible for degrading SDS into | ATCC 19151 where it is has been shown to be responsible for degrading SDS into | ||
− | 1-dodecanol.<br> | + | 1-dodecanol.<br><br> |
We plan to achieve this in three steps:<br> | We plan to achieve this in three steps:<br> | ||
● Extracellular release of SdsA1 by E.coli BL21(DE3) via attachment of N-terminal | ● Extracellular release of SdsA1 by E.coli BL21(DE3) via attachment of N-terminal | ||
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production of 1-dodecanol within the water sample.<br> | production of 1-dodecanol within the water sample.<br> | ||
● Separation and purification of 1-dodecanol from the sample. <br> | ● Separation and purification of 1-dodecanol from the sample. <br> | ||
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{{Template:IIT_Kanpur/Footer}} | {{Template:IIT_Kanpur/Footer}} |
Revision as of 16:09, 17 October 2018
Our Idea
Our aim is to extract 1-dodecanol(C12H26O) via in vitro degradation of Sodium Dodecyl
Sulphate (SDS) from contaminated water. This would be done in Escherichia coli(E.coli)
BL21(DE3) strain using alkyl sulfatase protein (SdsA1) derived from Pseudomonas sp.
ATCC 19151 where it is has been shown to be responsible for degrading SDS into
1-dodecanol.
We plan to achieve this in three steps:
● Extracellular release of SdsA1 by E.coli BL21(DE3) via attachment of N-terminal
secretion signal sequence pelB or OmpT.
● This is followed by the action of alkyl sulfatase(SdsA1) on SDS resulting in the
production of 1-dodecanol within the water sample.
● Separation and purification of 1-dodecanol from the sample.