Difference between revisions of "Part:BBa K5443002:Experience"
(2 intermediate revisions by 2 users not shown) | |||
Line 1: | Line 1: | ||
+ | ===Applications of BBa_K5443002=== | ||
+ | |||
+ | We showed that the Sam5 C3H enzyme was functional in <i>E. coli</i> as part of a vanillin biosynthetic pathway, as evidenced by production of caffeate (see LC-MS data from one clone pMQ3C-11, Fig. 1). Further evidence for functional expression of Sam5 was seen from production of a brown melanin-type dye as a side-reaction (see Fig. 2); we believe this indicates that Sam5 is acting on tyrosine (to make L-DOPA, which polymerises) in addition to our intended reaction on p-coumarate to make caffeate (caffeic acid). | ||
+ | |||
+ | |||
+ | <html> | ||
+ | <figure> | ||
+ | <img src="https://static.igem.wiki/teams/5443/pmq3c11-lcms-data-v2.jpg" style="width:600px;height:auto"> | ||
+ | <figcaption> | ||
+ | <b>Figure 1. LCMS analysis of compounds produced using pMQ3C-11.</b><br> | ||
+ | <i>The graph shows the detected presence of all 6 tested compounds, validating successful expression of all parts within pMQ3C-11, including Sam5.</i> | ||
+ | </figcaption> | ||
+ | </figure> | ||
+ | </html> | ||
+ | |||
+ | |||
+ | |||
+ | <html> | ||
+ | <figure> | ||
+ | <img src="https://static.igem.wiki/teams/5443/melanin-pmq3c.jpg" style="width:600px;height:auto"> | ||
+ | <figcaption> | ||
+ | <b>Figure 2. Patched clones of plasmid variants.</b><br> | ||
+ | <i>Each plate shows patched colonies transformed with variants of our created plasmids pMQ3B and pMQ3C. Some patched colonies show diffusion of a brown pigment into the surrounding agar, suggesting a side-reaction of the enzyme Sam5 that produces the brown pigment L-DOPA.</i> | ||
+ | </figcaption> | ||
+ | </figure> | ||
+ | </html> | ||
− | |||
− | |||
− | |||
− | |||
===User Reviews=== | ===User Reviews=== | ||
− | <!-- DON'T DELETE --><partinfo> | + | <!-- DON'T DELETE --><partinfo>BBa_K5443003 StartReviews</partinfo> |
<!-- Template for a user review | <!-- Template for a user review | ||
{|width='80%' style='border:1px solid gray' | {|width='80%' style='border:1px solid gray' | ||
|- | |- | ||
|width='10%'| | |width='10%'| | ||
− | <partinfo> | + | <partinfo>BBa_K5443003 AddReview number</partinfo> |
<I>Username</I> | <I>Username</I> | ||
|width='60%' valign='top'| | |width='60%' valign='top'| | ||
− | Enter the review | + | Enter the review information here. |
|}; | |}; | ||
<!-- End of the user review template --> | <!-- End of the user review template --> | ||
− | <!-- DON'T DELETE --><partinfo> | + | <!-- DON'T DELETE --><partinfo>BBa_K5443003 EndReviews</partinfo> |
Latest revision as of 13:51, 2 October 2024
Applications of BBa_K5443002
We showed that the Sam5 C3H enzyme was functional in E. coli as part of a vanillin biosynthetic pathway, as evidenced by production of caffeate (see LC-MS data from one clone pMQ3C-11, Fig. 1). Further evidence for functional expression of Sam5 was seen from production of a brown melanin-type dye as a side-reaction (see Fig. 2); we believe this indicates that Sam5 is acting on tyrosine (to make L-DOPA, which polymerises) in addition to our intended reaction on p-coumarate to make caffeate (caffeic acid).
User Reviews
UNIQe94efc970d888c3d-partinfo-00000002-QINU UNIQe94efc970d888c3d-partinfo-00000003-QINU