<?xml version="1.0" encoding="utf-8" standalone="yes"?><rss version="2.0" xmlns:atom="http://www.w3.org/2005/Atom"><channel><title>Biology on Jin Saeki Ko</title><link>https://jinsko.com/categories/biology/</link><description>Recent content in Biology on Jin Saeki Ko</description><generator>Hugo</generator><language>en-us</language><lastBuildDate>Fri, 19 Dec 2025 00:00:00 +0000</lastBuildDate><atom:link href="https://jinsko.com/categories/biology/index.xml" rel="self" type="application/rss+xml"/><item><title>Interbacterial Antagonism via Secretion Systems and its Applications</title><link>https://jinsko.com/blog/sec_systems/</link><pubDate>Fri, 19 Dec 2025 00:00:00 +0000</pubDate><guid>https://jinsko.com/blog/sec_systems/</guid><description>&lt;p&gt;Most antagonism doesn’t need contact. Bacteria just secrete stuff into the environment—for instance, specific bacteriocins and broad antibiotics. These diffuse and hit any nearby cells that don’t have the right resistance or immunity. This is a great example of long-range killing, with no direct contact needed&lt;sup id="fnref:1"&gt;&lt;a href="#fn:1" class="footnote-ref" role="doc-noteref"&gt;1&lt;/a&gt;&lt;/sup&gt;.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Type V secretion system:&lt;/strong&gt; the cell has a huge outer-membrane protein, CdiA, exported by CdiB. The N-terminal part of CdiA binds a specific receptor on the target cell. The C-terminal part (CdiA-CT) is the toxin domain that actually goes into the target and does the damage (DNase, RNase, translation block, etc.). The producing cell makes a small immunity protein, CdiI, that binds its own CdiA-CT and blocks it. So, if you have the matching &lt;em&gt;cdiI&lt;/em&gt; gene, you’re safe; if not, you get killed&lt;sup id="fnref:2"&gt;&lt;a href="#fn:2" class="footnote-ref" role="doc-noteref"&gt;2&lt;/a&gt;&lt;/sup&gt;.&lt;/p&gt;</description></item><item><title>Overview Of Sequencing</title><link>https://jinsko.com/blog/08-29-25/</link><pubDate>Fri, 29 Aug 2025 00:00:00 +0000</pubDate><guid>https://jinsko.com/blog/08-29-25/</guid><description>&lt;h2 id="1st-gen-sequencing"&gt;1st Gen Sequencing&lt;a href="#1st-gen-sequencing" class="heading-anchor" aria-label="Link to this section"&gt;&lt;svg class="h-4 w-4" aria-hidden="true" xmlns="http://www.w3.org/2000/svg" viewBox="0 0 24 24"&gt;&lt;g fill="none" stroke="currentColor" stroke-linecap="round" stroke-linejoin="round" stroke-width="2"&gt;&lt;path d="M10 13a5 5 0 0 0 7.54.54l3-3a5 5 0 0 0-7.07-7.07l-1.72 1.71"/&gt;&lt;path d="M14 11a5 5 0 0 0-7.54-.54l-3 3a5 5 0 0 0 7.07 7.07l1.71-1.71"/&gt;&lt;/g&gt;&lt;/svg&gt;&lt;/a&gt;&lt;/h2&gt;&lt;p&gt;Dideoxy gene sequencing uses what is called &amp;ldquo;primed synthesis&amp;rdquo; for sequencing. Primed synthesis works as follows: primers anneal onto a denatured strand of DNA, yielding ssDNA and creating a free 3&amp;rsquo;-OH group. A DNA polymerase then binds to the oligonucleotide primer, copying the remainder of the template strand. Understanding this mechanism is important for understanding the later stages of sequencing.&lt;/p&gt;</description></item></channel></rss>