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<title>GATE Overflow for GATE BT - Recent questions and answers in Recombinant DNA Technology</title>
<link>https://bt.gateoverflow.in/qa/recombinant-dna-technology-and-other-tools-in-biotechnology/recombinant-dna-technology</link>
<description>Powered by Question2Answer</description>
<item>
<title>GATE BT 2026 | Question: 16</title>
<link>https://bt.gateoverflow.in/1305/gate-bt-2026-question-16</link>
<description>&lt;p&gt;Which component of the $\text{CRISPR/Cas9}$ gene editing system is $\text{NOT}$ of natural origin?&lt;/p&gt;&lt;ol style=&quot;list-style-type:upper-alpha&quot;&gt;&lt;li&gt;$\text{CAS9}$ protein&lt;/li&gt;&lt;li&gt;$\text{CRISPR}$ repeats&lt;/li&gt;&lt;li&gt;$\text{PAM}$ sequence&lt;/li&gt;&lt;li&gt;$\text{sgRNA}$&lt;/li&gt;&lt;/ol&gt;</description>
<category>Recombinant DNA Technology</category>
<guid isPermaLink="true">https://bt.gateoverflow.in/1305/gate-bt-2026-question-16</guid>
<pubDate>Mon, 23 Feb 2026 14:21:50 +0000</pubDate>
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<title>Answered: If 1000 bp of a double-helical DNA weighs 18 1 10−  gm and distance between   two bp is0.34nm, the total amount of DNA (in mg, rounded off to one decimal  place) required to stretch from Earth to Moon (assuming the distance between  Earth and Moon to be 3,74,000 km) is ___________.</title>
<link>https://bt.gateoverflow.in/1118/helical-distance-required-assuming-distance-___________?show=1124#a1124</link>
<description>1.98mg ~ 2mg</description>
<category>Recombinant DNA Technology</category>
<guid isPermaLink="true">https://bt.gateoverflow.in/1118/helical-distance-required-assuming-distance-___________?show=1124#a1124</guid>
<pubDate>Mon, 19 Jan 2026 05:29:43 +0000</pubDate>
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<title>GATE BT 2025 | Question: 10</title>
<link>https://bt.gateoverflow.in/1069/gate-bt-2025-question-10</link>
<description>&lt;p&gt;​​​​​Which one of the following hosts is used in mammalian cell culture for the production of glycosylated recombinant therapeutic proteins?&lt;/p&gt;

&lt;ol start=&quot;1&quot; style=&quot;list-style-type:upper-alpha&quot;&gt;
	&lt;li&gt;Pichia pastoris&lt;/li&gt;
	&lt;li&gt;Sf$9$ cells&lt;/li&gt;
	&lt;li&gt;Escherichia coli&lt;/li&gt;
	&lt;li&gt;Chinese hamster ovary cells&lt;/li&gt;
&lt;/ol&gt;</description>
<category>Recombinant DNA Technology</category>
<guid isPermaLink="true">https://bt.gateoverflow.in/1069/gate-bt-2025-question-10</guid>
<pubDate>Thu, 06 Mar 2025 17:05:58 +0000</pubDate>
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<title>GATE BT 2023 | Question: 35</title>
<link>https://bt.gateoverflow.in/864/gate-bt-2023-question-35</link>
<description>&lt;p&gt;Which of the following vector(s) is(are) used to clone a &lt;strong&gt;DNA&lt;/strong&gt; fragment of size $220 \mathrm{~kb}$?&lt;/p&gt;

&lt;ol style=&quot;list-style-type:upper-alpha&quot;&gt;
	&lt;li&gt;Bacterial artificial chromosome&lt;/li&gt;
	&lt;li&gt;Yeast artificial chromosome&lt;/li&gt;
	&lt;li&gt;Cosmids&lt;/li&gt;
	&lt;li&gt;$\text{pUC19}$ plasmid
	&lt;p&gt;&amp;nbsp;&lt;/p&gt;
	&lt;/li&gt;
&lt;/ol&gt;</description>
<category>Recombinant DNA Technology</category>
<guid isPermaLink="true">https://bt.gateoverflow.in/864/gate-bt-2023-question-35</guid>
<pubDate>Sun, 21 May 2023 02:58:25 +0000</pubDate>
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<title>GATE BT 2022 | Question: 43</title>
<link>https://bt.gateoverflow.in/787/gate-bt-2022-question-43</link>
<description>&lt;p&gt;Introduction of foreign genes into plant cells can be carried out using&lt;/p&gt;

&lt;ol start=&quot;1&quot; style=&quot;list-style-type:upper-alpha&quot;&gt;
	&lt;li&gt;Agrobacterium&lt;/li&gt;
	&lt;li&gt;$\text{Cacl}_{2}$ mediated plasmid uptake&lt;/li&gt;
	&lt;li&gt;Electroporation&lt;/li&gt;
	&lt;li&gt;Gene gun&lt;/li&gt;
&lt;/ol&gt;</description>
<category>Recombinant DNA Technology</category>
<guid isPermaLink="true">https://bt.gateoverflow.in/787/gate-bt-2022-question-43</guid>
<pubDate>Sun, 20 Mar 2022 16:16:26 +0000</pubDate>
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<title>GATE2020: 37</title>
<link>https://bt.gateoverflow.in/622/gate2020-37</link>
<description>&lt;p&gt;The schematic of a plasmid with a gap in one of&amp;nbsp;the strands is shown below:&lt;/p&gt;

&lt;p&gt;&lt;img alt=&quot;&quot; src=&quot;https://bt.gateoverflow.in/?qa=blob&amp;amp;qa_blobid=16705722837080469970&quot;&gt;&lt;/p&gt;

&lt;p&gt;Which of the following enzyme(s) is/are required to fill the gap and generate a covalently closed circular plasmid?&lt;/p&gt;

&lt;ol start=&quot;16&quot; style=&quot;list-style-type:upper-alpha&quot; type=&quot;A&quot;&gt;
	&lt;li&gt;$DNA$&amp;nbsp;ligase&lt;/li&gt;
	&lt;li&gt;AIkaline phosphatase&lt;/li&gt;
	&lt;li&gt;$DNA$ polymerase&lt;/li&gt;
	&lt;li&gt;Polynucleotide kinase&lt;/li&gt;
&lt;/ol&gt;

&lt;ol style=&quot;list-style-type:upper-alpha&quot; type=&quot;A&quot;&gt;
	&lt;li&gt;$P$ only&lt;/li&gt;
	&lt;li&gt;$P, R$ and $S$ only&lt;/li&gt;
	&lt;li&gt;$P$ and $R$ only&lt;/li&gt;
	&lt;li&gt;$P, Q$ and $R$ only&lt;/li&gt;
&lt;/ol&gt;</description>
<category>Recombinant DNA Technology</category>
<guid isPermaLink="true">https://bt.gateoverflow.in/622/gate2020-37</guid>
<pubDate>Tue, 03 Nov 2020 11:16:26 +0000</pubDate>
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<title>GATE2020: 42</title>
<link>https://bt.gateoverflow.in/617/gate2020-42</link>
<description>&lt;p&gt;Determine the correctness or otherwise of the following Assertion [$a$] and the Reason [$r$].&lt;/p&gt;

&lt;p&gt;Assertion [$a$]: A genetically engineered rice that produces beta-carotene in the rice grain is called Golden rice&lt;/p&gt;

&lt;p&gt;Reason [$r$]: Enabling biosynthesis of provitamin $$A in the rice endosperm gives a characteristic yellow/orange color&lt;/p&gt;

&lt;ol style=&quot;list-style-type:upper-alpha&quot; type=&quot;A&quot;&gt;
	&lt;li&gt;Both [$a$] and [$r$]&amp;nbsp;are false&lt;/li&gt;
	&lt;li&gt;Both [$a$] and [$r$] are true but [$r$] is not the correct reason for [$a$]&lt;/li&gt;
	&lt;li&gt;Both [$a$] and [$r$] are true and&amp;nbsp;[$r$] is the correct reason for [$a$]&lt;/li&gt;
	&lt;li&gt;[$a$]&amp;nbsp;is true but [$r$] is false&lt;/li&gt;
&lt;/ol&gt;</description>
<category>Recombinant DNA Technology</category>
<guid isPermaLink="true">https://bt.gateoverflow.in/617/gate2020-42</guid>
<pubDate>Tue, 03 Nov 2020 11:14:30 +0000</pubDate>
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<title>GATE2020: 9</title>
<link>https://bt.gateoverflow.in/585/gate2020-9</link>
<description>&lt;p&gt;During a positive-negative selection process, transformed animal cells expressing __________________ are killed in presence of ganciclovir in the medium.&lt;/p&gt;

&lt;ol style=&quot;list-style-type:upper-alpha&quot; type=&quot;A&quot;&gt;
	&lt;li&gt;Pyruvate&amp;nbsp;kinase&lt;/li&gt;
	&lt;li&gt;viral thymidine kinase&lt;/li&gt;
	&lt;li&gt;viral serine/threonine&amp;nbsp;kinase&lt;/li&gt;
	&lt;li&gt;viral tyrosine&amp;nbsp;kinase&lt;/li&gt;
&lt;/ol&gt;</description>
<category>Recombinant DNA Technology</category>
<guid isPermaLink="true">https://bt.gateoverflow.in/585/gate2020-9</guid>
<pubDate>Tue, 03 Nov 2020 11:02:14 +0000</pubDate>
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<title>GATE2016-30</title>
<link>https://bt.gateoverflow.in/416/gate2016-30</link>
<description>&lt;p&gt;Select the CORRECT combination of genetic components that are essential for the transfer of T-DNA segment from &lt;em&gt;Agrobacterium tumefaciens&lt;/em&gt; to plant cells.&lt;/p&gt;

&lt;ol style=&quot;list-style-type:upper-alpha&quot;&gt;
	&lt;li&gt;Border repeat sequences and oncogenes&lt;/li&gt;
	&lt;li&gt;Border repeat sequences and &lt;em&gt;vir&lt;/em&gt; genes&lt;/li&gt;
	&lt;li&gt;Opine biosynthetic genes and &lt;em&gt;vir&lt;/em&gt; genes&lt;/li&gt;
	&lt;li&gt;Opine biosynthetic genes and oncogenes&lt;/li&gt;
&lt;/ol&gt;</description>
<category>Recombinant DNA Technology</category>
<guid isPermaLink="true">https://bt.gateoverflow.in/416/gate2016-30</guid>
<pubDate>Mon, 26 Mar 2018 16:59:49 +0000</pubDate>
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<title>GATE2016-36</title>
<link>https://bt.gateoverflow.in/410/gate2016-36</link>
<description>&lt;p&gt;A $1.2$ kb DNA fragment was cloned into $\textit{Bam}$HI and $\textit{Eco}$RI sites located on a $2.8$ kb cloning vector. The $\textit{Bam}$HI and $\textit{Eco}$RI sites are adjacent to each other on the vector backbone. The vector contains an $\textit{XhoI}$ site located $300$ bp upstream of the $\textit{Bam}$HI site. An internal $\textit{XhoI}$ site is present in the gene sequence as shown in the figure. The resultant recombinant plasmid is digested with $\textit{Eco}$RI and $\textit{Xhol}$ and analyzed through $1 \%$ agarose gel electrophoresis. Assuming complete digestion with $\textit{Eco}$RI and&amp;nbsp;$\textit{Xhol}$, the DNA fragments (in base pairs) visible on the agarose gel will correspond to:&lt;/p&gt;

&lt;p&gt;&lt;img alt=&quot;&quot; src=&quot;https://bt.gateoverflow.in/?qa=blob&amp;amp;qa_blobid=15199034373576732285&quot;&gt;&lt;/p&gt;

&lt;ol style=&quot;list-style-type:upper-alpha&quot;&gt;
	&lt;li&gt;$2800$, $700$ and $500$&lt;/li&gt;
	&lt;li&gt;$2800$, $700$ and $800$&lt;/li&gt;
	&lt;li&gt;$2500$, $700$ and $800$&lt;/li&gt;
	&lt;li&gt;$2500$, $1200$ and $300$&lt;/li&gt;
&lt;/ol&gt;</description>
<category>Recombinant DNA Technology</category>
<guid isPermaLink="true">https://bt.gateoverflow.in/410/gate2016-36</guid>
<pubDate>Mon, 26 Mar 2018 16:59:48 +0000</pubDate>
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<title>GATE BT 2017 | Question: 42</title>
<link>https://bt.gateoverflow.in/349/gate-bt-2017-question-42</link>
<description>&lt;p&gt;A recombinant protein is to be expressed under the control of the &lt;em&gt;lac&amp;nbsp;&lt;/em&gt;promoter and operator in a strain&amp;nbsp;$\textit{E.coli}$&amp;nbsp;having the genotype &lt;em&gt;lac&lt;/em&gt;I$^+$ &lt;em&gt;crp$^+$&lt;/em&gt;&amp;nbsp;.&amp;nbsp;Even in the absence of inducer IPTG, low levels of expression of the recombinant protein are seen (leaky expression). Which one of the following should be done to minimize such leaky expression?&lt;/p&gt;

&lt;ol style=&quot;list-style-type:upper-alpha&quot; type=&quot;A&quot;&gt;
	&lt;li&gt;Addition of lactose to the medium&lt;/li&gt;
	&lt;li&gt;Removal of all glucose from the medium&lt;/li&gt;
	&lt;li&gt;Addition of excess glucose to the medium&lt;/li&gt;
	&lt;li&gt;Addition of &lt;em&gt;allo&lt;/em&gt;-lactose to the medium&lt;/li&gt;
&lt;/ol&gt;</description>
<category>Recombinant DNA Technology</category>
<guid isPermaLink="true">https://bt.gateoverflow.in/349/gate-bt-2017-question-42</guid>
<pubDate>Mon, 26 Mar 2018 16:43:16 +0000</pubDate>
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<title>GATE BT 2017 | Question: 43</title>
<link>https://bt.gateoverflow.in/348/gate-bt-2017-question-43</link>
<description>&lt;p&gt;Shown below id a plasmid vector (P) and an insert (Q). The insert was cloned into the &lt;em&gt;Bam&lt;/em&gt;HI site of the vector. The recombinant plasmid was isolated and digested with&amp;nbsp;&lt;em&gt;Bam&lt;/em&gt;Hi or&amp;nbsp;&lt;em&gt;Xho&lt;/em&gt;I. The results from the digestion experiments are shown in (R)&lt;/p&gt;

&lt;p&gt;&lt;img alt=&quot;&quot; src=&quot;https://bt.gateoverflow.in/?qa=blob&amp;amp;qa_blobid=988722321335445199&quot;&gt;&lt;br&gt;
&lt;br&gt;
Which one of the following explains the digestion results shown in (R)&lt;/p&gt;

&lt;ol style=&quot;list-style-type:upper-alpha&quot; type=&quot;A&quot;&gt;
	&lt;li&gt;The insert did not ligate to the vector.&lt;/li&gt;
	&lt;li&gt;One copy of the insert ligated to the vector.&lt;/li&gt;
	&lt;li&gt;The insert ligated to the Vector as two tandem copies&lt;/li&gt;
	&lt;li&gt;The insert ligated to the vector as two copies but not in tandem&lt;/li&gt;
&lt;/ol&gt;</description>
<category>Recombinant DNA Technology</category>
<guid isPermaLink="true">https://bt.gateoverflow.in/348/gate-bt-2017-question-43</guid>
<pubDate>Mon, 26 Mar 2018 16:43:16 +0000</pubDate>
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<title>GATE BT 2015 | Question: 13</title>
<link>https://bt.gateoverflow.in/313/gate-bt-2015-question-13</link>
<description>&lt;p&gt;Which one of the following is a second generation genetically engineered crop?&lt;/p&gt;

&lt;ol style=&quot;list-style-type:upper-alpha&quot;&gt;
	&lt;li&gt;Bt brinjal&lt;/li&gt;
	&lt;li&gt;Roundup soyabean&lt;/li&gt;
	&lt;li&gt;Golden rice&lt;/li&gt;
	&lt;li&gt;Bt rice&lt;/li&gt;
&lt;/ol&gt;</description>
<category>Recombinant DNA Technology</category>
<guid isPermaLink="true">https://bt.gateoverflow.in/313/gate-bt-2015-question-13</guid>
<pubDate>Mon, 26 Mar 2018 15:10:50 +0000</pubDate>
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<item>
<title>GATE BT 2015 | Question: 23</title>
<link>https://bt.gateoverflow.in/303/gate-bt-2015-question-23</link>
<description>&lt;p&gt;Which one of the following features is NOT required in a prokaryotic expression vector?&lt;/p&gt;

&lt;ol style=&quot;list-style-type:upper-alpha&quot;&gt;
	&lt;li&gt;$\textit{oriC}$&lt;/li&gt;
	&lt;li&gt;Selection marker&lt;/li&gt;
	&lt;li&gt;CMV promoter&lt;/li&gt;
	&lt;li&gt;Ribosome binding site&lt;/li&gt;
&lt;/ol&gt;</description>
<category>Recombinant DNA Technology</category>
<guid isPermaLink="true">https://bt.gateoverflow.in/303/gate-bt-2015-question-23</guid>
<pubDate>Mon, 26 Mar 2018 15:10:48 +0000</pubDate>
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<title>GATE BT 2012 | Question: 2</title>
<link>https://bt.gateoverflow.in/67/gate-bt-2012-question-2</link>
<description>&lt;p&gt;The basis for blue-white screening with $pUC$ vectors is&lt;/p&gt;

&lt;ol style=&quot;list-style-type:upper-alpha&quot;&gt;
	&lt;li&gt;intraallelic complementation&lt;/li&gt;
	&lt;li&gt;intergenic complementation&lt;/li&gt;
	&lt;li&gt;intragenic suppression&lt;/li&gt;
	&lt;li&gt;extragenic suppression&lt;/li&gt;
&lt;/ol&gt;</description>
<category>Recombinant DNA Technology</category>
<guid isPermaLink="true">https://bt.gateoverflow.in/67/gate-bt-2012-question-2</guid>
<pubDate>Sun, 25 Mar 2018 08:38:41 +0000</pubDate>
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