<?xml version="1.0" encoding="utf-8" standalone="yes"?><rss version="2.0" xmlns:atom="http://www.w3.org/2005/Atom"><channel><title>Sofya Rakitina — HTBAA Fall 2026 :: 2026a-sofya-rakitina</title><link>https://pages.htgaa.org/2026b/sofya-rakitina/index.html</link><description>About me 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><atom:link href="https://pages.htgaa.org/2026b/sofya-rakitina/index.xml" rel="self" type="application/rss+xml"/><item><title>Week 1 HW: Final Project Ideas</title><link>https://pages.htgaa.org/2026b/sofya-rakitina/week-01-hw-project-ideas/index.html</link><pubDate>Mon, 01 Jan 0001 00:00:00 +0000</pubDate><guid>https://pages.htgaa.org/2026b/sofya-rakitina/week-01-hw-project-ideas/index.html</guid><description>(1) What you would like to biomanufacture and why?&#10;With this project, I was really lost in what to make for a while, but I was definitely hoping to produce something within the realm of materials, so I ended up having a quick chat with some people in the lab about what I could do and was told about BC and how that could be a great starting point. I’m considering designing something related to tech, or improving it, whether that’s tactile interfacing, or extensions of HCI through hardware.</description></item><item><title>Week 2 HW: DNA Design &amp; Applications</title><link>https://pages.htgaa.org/2026b/sofya-rakitina/week-02-hw-dna-design/index.html</link><pubDate>Mon, 01 Jan 0001 00:00:00 +0000</pubDate><guid>https://pages.htgaa.org/2026b/sofya-rakitina/week-02-hw-dna-design/index.html</guid><description>Here’s a link to the created folder: https://kernel.asimov.com/htgaa-2026/repositories/repository/ac213b04-6666-415f-a63e-a313df44690a/folder/8dea22af-bfa2-4e02-9b92-9adb7c61c1a8 Repository: Lifefabs HTBAA 2026; folder: rakitina-bc.&#10;Part 1: Define your expression target&#10;Okay, so to reinstate it again what I want to do is to make a swappable bacterial cellulose (BC) sensor insert for a wearable, sort of mouse-like input device, with Komagataeibacter (possibly) producing the cellulose and an engineered melanin-producing organism providing pigmentation/conductive functionality. This also made me realise that I have 2 parts to my overall manufacturing system. One should be designed for enhancing/controlling bacterial cellulose production in Komagataeibacter xylinus, and then also there’s one for melanin production in engineered E. coli. As for the final material, I’m going to co-culture them to get a melanised BC sensor.</description></item><item><title>Week 3 HW: Cell-Free Protocols</title><link>https://pages.htgaa.org/2026b/sofya-rakitina/week-03-hw-cell-free/index.html</link><pubDate>Mon, 01 Jan 0001 00:00:00 +0000</pubDate><guid>https://pages.htgaa.org/2026b/sofya-rakitina/week-03-hw-cell-free/index.html</guid><description>A. COMPARE CELL-FREE REACTION COMPOSITIONS (20 minutes)&#10;Why does the concentration of potassium glutamate and magnesium glutamate differ between compositions? Which is more sensitive? Here’s how the data describes both on the https://coopetition.htgaa.org/cfps :&#10;“Potassium is the main salt needed for ribosomes to work. Glutamate replaces chloride as the counter-ion because chloride inhibits some CFPS enzymes. Getting the right K⁺ concentration is one of the biggest tuning levers in CFPS. Reteplase Reteplase needs lower K(Glu) (~250 mM) than sfGFP (~354 mM) to reduce aggregation during synthesis”</description></item><item><title>Final Project</title><link>https://pages.htgaa.org/2026b/sofya-rakitina/final-project/index.html</link><pubDate>Mon, 01 Jan 0001 00:00:00 +0000</pubDate><guid>https://pages.htgaa.org/2026b/sofya-rakitina/final-project/index.html</guid><description/></item></channel></rss>