<?xml version="1.0" encoding="utf-8" standalone="yes"?><rss version="2.0" xmlns:atom="http://www.w3.org/2005/Atom"><channel><title>&lt;MEHMET ERKAN OZSEYHAN&gt; — HTBAA Fall 2026 :: mehmet-erkan-ozseyhan</title><link>https://pages.htgaa.org/2026b/mehmet-erkan-ozseyhan/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/mehmet-erkan-ozseyhan/index.xml" rel="self" type="application/rss+xml"/><item><title>Week 1 HW: Final Project Ideas</title><link>https://pages.htgaa.org/2026b/mehmet-erkan-ozseyhan/week-01-hw-project-ideas/index.html</link><pubDate>Mon, 01 Jan 0001 00:00:00 +0000</pubDate><guid>https://pages.htgaa.org/2026b/mehmet-erkan-ozseyhan/week-01-hw-project-ideas/index.html</guid><description>1.&#9;What do you want to make? → An engineered trehalose-overproducing rhizobacterium, applied as a dry seed coating on rainfed wheat, that manufactures drought-priming signal continuously at the root instead of delivering it once as a chemical.&#10;2.&#9;What living system could make it? → Azospirillum brasilense (or a Bacillus backup for shelf life) carrying a bifunctional yeast TPS–TPP fusion under an osmotically inducible promoter. In: seed, soil water, root exudate carbon. Out: a colonized, stress-primed root system.</description></item><item><title>Week 2 HW: DNA Design</title><link>https://pages.htgaa.org/2026b/mehmet-erkan-ozseyhan/week-02-hw-dna-design/index.html</link><pubDate>Mon, 01 Jan 0001 00:00:00 +0000</pubDate><guid>https://pages.htgaa.org/2026b/mehmet-erkan-ozseyhan/week-02-hw-dna-design/index.html</guid><description>Part 0: Setup in Benchling Repository Name: Project/MIT HTBAA 2026&#10;Project Name: Engineered trehalose-overproducing rhizobacterial seed inoculant for rainfed wheat&#10;Part 1: Expression Target What molecule am I expressing?&#10;A single bifunctional trehalose-6-phosphate synthase / trehalose-6-phosphate phosphatase (TPS–TPP) fusion enzyme of 892 amino acids: one polypeptide carrying two sequential catalytic activities. TPS (EC 2.4.1.15) condenses UDP-glucose and glucose-6-phosphate to trehalose-6-phosphate (T6P); TPP (EC 3.1.3.12) then dephosphorylates T6P to trehalose. Expressing this as one fusion rather than two genes is a deliberate design choice with three justifications, two of them drawn directly from the source literature:</description></item><item><title>Week 3 HW: Cell-Free Protocols</title><link>https://pages.htgaa.org/2026b/mehmet-erkan-ozseyhan/week-03-hw-cell-free/index.html</link><pubDate>Mon, 01 Jan 0001 00:00:00 +0000</pubDate><guid>https://pages.htgaa.org/2026b/mehmet-erkan-ozseyhan/week-03-hw-cell-free/index.html</guid><description>Section A A1. Why K-glutamate and Mg-glutamate concentrations differ — and which is more sensitive Potassium Glutamate (K-Glu, ~100–200 mM) — Bulk Counterion: Serves as the primary salt to set the ionic strength and osmolarity to mimic the cellular environment (E. coli cytoplasm) and stabilize ribosome/tRNA structures. It has low sensitivity because its optimal range is broad and forgiving (typically ±30–50 mM).</description></item><item><title>Final Project</title><link>https://pages.htgaa.org/2026b/mehmet-erkan-ozseyhan/final-project/index.html</link><pubDate>Mon, 01 Jan 0001 00:00:00 +0000</pubDate><guid>https://pages.htgaa.org/2026b/mehmet-erkan-ozseyhan/final-project/index.html</guid><description/></item></channel></rss>