<?xml version="1.0" encoding="utf-8"?>
<journal>
<title>Reports of Biochemistry and Molecular Biology</title>
<title_fa></title_fa>
<short_title>rbmb.net</short_title>
<subject>Basic Sciences</subject>
<web_url>http://rbmb.net</web_url>
<journal_hbi_system_id>1</journal_hbi_system_id>
<journal_hbi_system_user>admin</journal_hbi_system_user>
<journal_id_issn>2322-3480</journal_id_issn>
<journal_id_issn_online>2322-3480</journal_id_issn_online>
<journal_id_pii></journal_id_pii>
<journal_id_doi>10.61882/rbmb</journal_id_doi>
<journal_id_iranmedex></journal_id_iranmedex>
<journal_id_magiran></journal_id_magiran>
<journal_id_sid></journal_id_sid>
<journal_id_nlai></journal_id_nlai>
<journal_id_science></journal_id_science>
<language>en</language>
<pubdate>
	<type>jalali</type>
	<year>1401</year>
	<month>5</month>
	<day>1</day>
</pubdate>
<pubdate>
	<type>gregorian</type>
	<year>2022</year>
	<month>8</month>
	<day>1</day>
</pubdate>
<volume>11</volume>
<number>2</number>
<publish_type>online</publish_type>
<publish_edition>1</publish_edition>
<article_type>fulltext</article_type>
<articleset>
	<article>


	<language>en</language>
	<article_id_doi></article_id_doi>
	<title_fa></title_fa>
	<title>Isolated Diaphorase From Bovine Erythrocyte Cannot Reduce Oxidized Cytoglobin (Metcygb)</title>
	<subject_fa>بیوشیمی</subject_fa>
	<subject>Biochemistry</subject>
	<content_type_fa>مقالات اصلی</content_type_fa>
	<content_type>Original Article</content_type>
	<abstract_fa></abstract_fa>
	<abstract>&lt;div style=&quot;text-align: justify;&quot;&gt;&lt;strong&gt;&lt;em&gt;Background: &lt;/em&gt;&lt;/strong&gt;Cytoglobin (Cygb) is a relatively newly identified globin protein that acts as an oxygen&amp;nbsp;transporter in tissues like hemoglobin (Hb) in erythrocytes and myoglobin (Mb) in muscles. The natural&amp;nbsp;oxidation of the Fe2+ ion in its heme group into metglobin (globin-Fe3+) made the loses of oxygen binding&amp;nbsp;functions. It is known metHb and metMb can be reduced enzymatically using diaphorase or cyb5r3.&amp;nbsp;However, metCygb reductase had not been previously identified. This study aims to analyze the reducing&amp;nbsp;activity of bovine diaphorase on metCygb.&lt;br&gt;
&lt;br&gt;
&lt;em&gt;&lt;strong&gt;Methods:&lt;/strong&gt;&lt;/em&gt; Diaphorase was isolated from bovine erythrocyte and purified using gel filtration and cationicexchanger&amp;nbsp;chromatography. Its purity was verified by SDS-PAGE and western blot (WB). The metCygb&amp;nbsp;was obtained from Cygb oxidation with potassium ferrocyanide and its reducing activity was determined&amp;nbsp;by spectroscopy.&lt;br&gt;
&lt;br&gt;
&lt;strong&gt;&lt;em&gt;Results:&lt;/em&gt;&lt;/strong&gt; The diaphorase (MW=30.09 kDa) was purified 10.77-fold from crude enzyme with specific&amp;nbsp;activity against metHb 8.479 U/mg. The purity was confirmed by WB using primary antibody anti-cyb5r3.&amp;nbsp;The purified enzyme reduced metCygb at 0.785 &amp;mu;gmin-1, which was 13.7 times less than the Vmax of&amp;nbsp;metHb.&lt;br&gt;
&lt;br&gt;
&lt;em&gt;&lt;strong&gt;Conclusions:&lt;/strong&gt;&lt;/em&gt; In conclusion, the purified diaphorase from bovine erythrocytes did not significantly reduce&amp;nbsp;metCygb rather than metHb, a natural substrate in cells.&lt;/div&gt;</abstract>
	<keyword_fa></keyword_fa>
	<keyword>Bovine Erythrocyte, Cytochrome B5 Reductase, Diaphorase, Metcytoglobin, Reduction.</keyword>
	<start_page>289</start_page>
	<end_page>298</end_page>
	<web_url>http://rbmb.net/browse.php?a_code=A-10-946-1&amp;slc_lang=en&amp;sid=1</web_url>


<author_list>
	<author>
	<first_name>Gissi </first_name>
	<middle_name></middle_name>
	<last_name>Novientri</last_name>
	<suffix></suffix>
	<first_name_fa></first_name_fa>
	<middle_name_fa></middle_name_fa>
	<last_name_fa></last_name_fa>
	<suffix_fa></suffix_fa>
	<email></email>
	<code>100319475328460012989</code>
	<orcid>100319475328460012989</orcid>
	<coreauthor>No</coreauthor>
	<affiliation>Master Program of Biomedical Sciences, Faculty of Medicine, Universitas Indonesia, Jakarta, Indonesia.</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>Mohamad</first_name>
	<middle_name></middle_name>
	<last_name> Sadikin</last_name>
	<suffix></suffix>
	<first_name_fa></first_name_fa>
	<middle_name_fa></middle_name_fa>
	<last_name_fa></last_name_fa>
	<suffix_fa></suffix_fa>
	<email>sadikinmohamad@gmail.com.</email>
	<code>100319475328460012990</code>
	<orcid>100319475328460012990</orcid>
	<coreauthor>Yes
</coreauthor>
	<affiliation>Department of Biochemistry and Molecular Biology, Faculty of Medicine, Universitas Indonesia, Jakarta, Indonesia &amp; Center of Hypoxia and Oxidative Stress Studies, Faculty of Medicine, Universitas Indonesia.</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


	<author>
	<first_name>Sri</first_name>
	<middle_name></middle_name>
	<last_name>Widia Jusman</last_name>
	<suffix></suffix>
	<first_name_fa></first_name_fa>
	<middle_name_fa></middle_name_fa>
	<last_name_fa></last_name_fa>
	<suffix_fa></suffix_fa>
	<email></email>
	<code>100319475328460012991</code>
	<orcid>100319475328460012991</orcid>
	<coreauthor>No</coreauthor>
	<affiliation>Department of Biochemistry and Molecular Biology, Faculty of Medicine, Universitas Indonesia, Jakarta, Indonesia &amp;  Center of Hypoxia and Oxidative Stress Studies, Faculty of Medicine, Universitas Indonesia</affiliation>
	<affiliation_fa></affiliation_fa>
	 </author>


</author_list>


	</article>
</articleset>
</journal>
