<?xml version="1.0" encoding="utf-8" standalone="yes"?><rss version="2.0" xmlns:atom="http://www.w3.org/2005/Atom"><channel><title>Jamie Dixon — HTBAA Fall 2026 :: jamie-dixon</title><link>https://pages.htgaa.org/2026b/jamie-dixon/index.html</link><description>About me Colorado Sweet Potato King&#10;Contact info Homework, Labs, and Projects See the nav bar on the left to look through my work for How To Biomanufacture Almost Anything (Fall 2026)!</description><generator>Hugo</generator><language>en</language><lastBuildDate>Sun, 04 Oct 2026 00:00:00 +0000</lastBuildDate><atom:link href="https://pages.htgaa.org/2026b/jamie-dixon/index.xml" rel="self" type="application/rss+xml"/><item><title>Week 1 HW: Final Project Ideas</title><link>https://pages.htgaa.org/2026b/jamie-dixon/week-01-hw-project-ideas/index.html</link><pubDate>Mon, 01 Jan 0001 00:00:00 +0000</pubDate><guid>https://pages.htgaa.org/2026b/jamie-dixon/week-01-hw-project-ideas/index.html</guid><description>HTBAA Homework #1 Due: Tuesday September 22, by 2:30p ET&#10;For your first homework, propose and describe one idea for something you would like to biomanufacture. This could be medicine, material, food, energy, an art, design, or architectural artifact, or beyond. Draw from your own background and interests for inspiration.&#10;(1)&#9;What you would like to biomanufacture and why? Describe the target product or output you would like to make.</description></item><item><title>Week 2 HW: DNA Design</title><link>https://pages.htgaa.org/2026b/jamie-dixon/week-02-hw-dna-design/index.html</link><pubDate>Mon, 01 Jan 0001 00:00:00 +0000</pubDate><guid>https://pages.htgaa.org/2026b/jamie-dixon/week-02-hw-dna-design/index.html</guid><description>Overview&#10;The steps to create a CBB resistant coffee tree Does not work: altering the genome of the tree using CRISPR of the tree b/c no one know how to do it - what site expresses the cherries for example&#10;What will works: altering the genome of the tree using a protein that destroys the gut of the CBB 1) Get the cry10Aa sequence and design the full expression cassette. 2) Order the synthesized cassette from Twist, cloned into your binary vector. 3) Amplify the plasmid in E. coli and verify it. 4) Transform Agrobacterium with the purified plasmid. 5) Co-culture with coffee somatic embryos, then select on antibiotic. 6) Regenerate plants, confirm the insert (PCR or Southern blot), and bioassay against the borer. Why the cry10Aa sequeence works 1) The insect eats the protein. A borer chewing into the berry ingests the toxin along with plant tissue. 2) The gut activates it. Insect midguts are typically alkaline and full of proteases, which convert the protein into its active form. 3) It binds gut receptors. The active toxin attaches to specific receptors on the midgut lining cells. The article notes that Cry proteins work this way, and that it's why organisms lacking the right receptors aren't affected. 4) The cells rupture. Binding leads to pores forming in the membrane, and the gut cells burst. 5) The insect dies. The damaged gut lets gut contents and bacteria leak into the body cavity, causing septicemia. What molecule am I expressing?</description></item><item><title>Final Project</title><link>https://pages.htgaa.org/2026b/jamie-dixon/final-project/index.html</link><pubDate>Mon, 01 Jan 0001 00:00:00 +0000</pubDate><guid>https://pages.htgaa.org/2026b/jamie-dixon/final-project/index.html</guid><description/></item><item><title>Week 3 HW: Cell-Free Reaction Design (Coopetition)</title><link>https://pages.htgaa.org/2026b/jamie-dixon/week-03-hw-coopetition/index.html</link><pubDate>Sun, 04 Oct 2026 00:00:00 +0000</pubDate><guid>https://pages.htgaa.org/2026b/jamie-dixon/week-03-hw-coopetition/index.html</guid><description>Week 3 Homework: Designing a Cell-Free Reaction Composition Due: Tuesday, October 6, 2026&#10;Coopetition website: coopetition.htgaa.org&#10;Goal: Using the collective intelligence of the HTBAA community and accessible AI systems, design novel cell-free protein synthesis (CFPS) reaction compositions for each of the three target proteins (sfGFP, PETase, and Reteplase) to reduce the cost per gram of functional protein. Each design should be compatible with the experimental framework and reflect the distinct expression and folding requirements of that protein.</description></item></channel></rss>