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<Article>
<Journal>
				<PublisherName>Iranian Research Organization for Science and Technology (IROST)</PublisherName>
				<JournalTitle>Microbiology, Metabolites and Biotechnology</JournalTitle>
				<Issn>2980-8855</Issn>
				<Volume>8</Volume>
				<Issue>1</Issue>
				<PubDate PubStatus="epublish">
					<Year>2025</Year>
					<Month>06</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Prevalence of bap and ompA immune evasion genes, biofilm formation ability, antibiotic resistance pattern, and motility of Acinetobacter baumannii</ArticleTitle>
<VernacularTitle></VernacularTitle>
			<FirstPage>1</FirstPage>
			<LastPage>7</LastPage>
			<ELocationID EIdType="pii">1556</ELocationID>
			
<ELocationID EIdType="doi">10.22104/mmb.2025.7463.1167</ELocationID>
			
			<Language>EN</Language>
<AuthorList>
<Author>
					<FirstName>Hafez</FirstName>
					<LastName>Mozayyan Esfahani</LastName>
<Affiliation>Department of Cell and Molecular Biology &amp; Microbiology, Faculty of Biological Science and Technology, University of Isfahan, Isfahan, Iran.</Affiliation>

</Author>
<Author>
					<FirstName>Babak</FirstName>
					<LastName>Beikzadeh</LastName>
<Affiliation>Department of Cell and Molecular Biology &amp; Microbiology, Faculty of Biological Science and Technology, University of Isfahan, Isfahan, Iran.</Affiliation>

</Author>
<Author>
					<FirstName>Soodabeh</FirstName>
					<LastName>Rostami</LastName>
<Affiliation>Infectious Diseases and Tropical Medicine Research Center, Isfahan University of Medical Sciences, Isfahan, Iran.</Affiliation>

</Author>
<Author>
					<FirstName>Mohammad</FirstName>
					<LastName>Rabbani Khorasgani</LastName>
<Affiliation>Department of Cell and Molecular Biology &amp; Microbiology, Faculty of Biological Science and Technology, University of Isfahan, Isfahan, Iran.</Affiliation>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2025</Year>
					<Month>03</Month>
					<Day>29</Day>
				</PubDate>
			</History>
		<Abstract>&lt;em&gt;Acinetobacter baumannii&lt;/em&gt; (&lt;em&gt;A. baumannii&lt;/em&gt;) is recognized as a significant pathogen responsible for hospital-acquired infections. This research aims to investigate the frequency of &lt;em&gt;bap&lt;/em&gt; and &lt;em&gt;ompA&lt;/em&gt; immune evasion genes, thereby determining the profile of antibiotic resistance in bacteria and the biofilm-producing ability among isolates obtained from patients with respiratory infections in Isfahan, Iran. In the present study, among 100 isolates collected from respiratory tract infections, 96 isolates were confirmed as &lt;em&gt;A. baumannii&lt;/em&gt; by biochemical tests and molecular analysis. The presence of &lt;em&gt;bap&lt;/em&gt; and &lt;em&gt;ompA&lt;/em&gt; genes in these isolates was checked by PCR, and antibiotic susceptibility was assessed using the disc diffusion method. Finally, the ability to form biofilm and motility were investigated. Results showed that 100% of the isolates carried the &lt;em&gt;ompA&lt;/em&gt; gene. However, for the &lt;em&gt;bap&lt;/em&gt; gene, 95.83% of isolates were positive. Investigation of antibiotic resistance showed that &lt;em&gt;A. baumannii&lt;/em&gt; isolates exhibited resistance to most antibiotics. The results of the biofilm test revealed that 97.91% of the isolates could form biofilm, including 39.58% with weak biofilm, 44.79% with medium biofilm, and 13.54% with strong biofilm, leaving the remaining 2% unable to form biofilm. Moreover, our results show that 6.4% of isolates were non-motile, 45.9% had an intermediate ability for twitching motility, and 47.7% showed a high ability for twitching motility. No correlation was observed between twitching motility, biofilm production, and antibiotic resistance. The present study demonstrates that the &lt;em&gt;bap&lt;/em&gt; and &lt;em&gt;ompA&lt;/em&gt; genes are highly abundant in lung infections, and most of these isolates are multidrug-resistant, exhibiting a high ability to form biofilms and display motility.</Abstract>
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			<Param Name="value">Twitching motility</Param>
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			<Param Name="value">Respiratory Infection</Param>
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			<Object Type="keyword">
			<Param Name="value">Hospital-acquired infections</Param>
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			<Object Type="keyword">
			<Param Name="value">multidrug-resistant</Param>
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<Article>
<Journal>
				<PublisherName>Iranian Research Organization for Science and Technology (IROST)</PublisherName>
				<JournalTitle>Microbiology, Metabolites and Biotechnology</JournalTitle>
				<Issn>2980-8855</Issn>
				<Volume>8</Volume>
				<Issue>1</Issue>
				<PubDate PubStatus="epublish">
					<Year>2025</Year>
					<Month>06</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Enhancing Aloe Vera growth and secondary metabolite production using an alternating magnetic field</ArticleTitle>
<VernacularTitle></VernacularTitle>
			<FirstPage>8</FirstPage>
			<LastPage>13</LastPage>
			<ELocationID EIdType="pii">1510</ELocationID>
			
<ELocationID EIdType="doi">10.22104/mmb.2025.7204.1155</ELocationID>
			
			<Language>EN</Language>
<AuthorList>
<Author>
					<FirstName>Majid</FirstName>
					<LastName>Masoumian</LastName>
<Affiliation>Department of Agriculture, Iranian Research Organization for Science and Technology (IROST), Tehran</Affiliation>

</Author>
<Author>
					<FirstName>Mohammad</FirstName>
					<LastName>Zangi</LastName>
<Affiliation>Department of Agriculture, Islamic Azad University, Damghan, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Rouzbeh</FirstName>
					<LastName>Abbaszadeh</LastName>
<Affiliation>Department of Agriculture, Iranian Research Organization for Science and Technology (IROST), Tehran</Affiliation>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2024</Year>
					<Month>11</Month>
					<Day>05</Day>
				</PubDate>
			</History>
		<Abstract>Magnetic field can be used as a physical elicitor to increase secondary metabolite in medicinal plants. In this research, the effects of alternating magnetic stress on production of flavonoids and growth parameters of &lt;em&gt;Aloe vera&lt;/em&gt; were studied. Number of weeks, magnetic flux density, and exposure time are effective parameters that have been changed in this experiment. In order to apply alternating magnetic field, a system was designed and built, including Helm Holtz coil, auto-transformer, multi meter, and Tesla meter. Control samples were grown without magnetic field.  All samples were kept in growth chamber at a temperature of 24 ± 2° C and 16-hour light, 8-hour dark photoperiod. Factorial experiment based on RCD used to test magnetic field effects on selected traits. According to the obtained results, the magnetic field was effective on secondary metabolite production. 38.44 mg/g DW flavonoid was produced by with flux density of 1.5 mT and 45 min per day exposure times for two weeks. The maximum number of leaves was observed in 0.5 mT and 135 min per day exposure times. In addition, the highest plant was produced after three weeks with 0.5 mT. The week, exposure time and the magnetic flux density have second order interaction. It seems that the magnetic field can be both harmful and beneficial for &lt;em&gt;Aloe vera&lt;/em&gt; that is dependent on various factors. In order to achieve the desired result, optimum field should be used.</Abstract>
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			<Param Name="value">Electro-culture</Param>
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			<Object Type="keyword">
			<Param Name="value">Medicinal plant</Param>
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<ArchiveCopySource DocType="pdf">https://mmb.irost.ir/article_1510_13cf7034f104d54e87c25fee462c7fc0.pdf</ArchiveCopySource>
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<Article>
<Journal>
				<PublisherName>Iranian Research Organization for Science and Technology (IROST)</PublisherName>
				<JournalTitle>Microbiology, Metabolites and Biotechnology</JournalTitle>
				<Issn>2980-8855</Issn>
				<Volume>8</Volume>
				<Issue>1</Issue>
				<PubDate PubStatus="epublish">
					<Year>2025</Year>
					<Month>06</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Biotechnological Applications of Selected Plant Species in Iraqi Kurdistan</ArticleTitle>
<VernacularTitle></VernacularTitle>
			<FirstPage>14</FirstPage>
			<LastPage>36</LastPage>
			<ELocationID EIdType="pii">1555</ELocationID>
			
<ELocationID EIdType="doi">10.22104/mmb.2025.7414.1165</ELocationID>
			
			<Language>EN</Language>
<AuthorList>
<Author>
					<FirstName>Selar Shawkat</FirstName>
					<LastName>Izzat</LastName>
<Affiliation>Department of Biology, College of Science, University of Sulaimani, 46001 Sulaymaniyah-Iraq</Affiliation>

</Author>
<Author>
					<FirstName>Honey Azad</FirstName>
					<LastName>Salih</LastName>
<Affiliation>Department of Biology, College of Science, University of Sulaimani, 46001 Sulaymaniyah-Iraq</Affiliation>

</Author>
<Author>
					<FirstName>Hawbash Fars</FirstName>
					<LastName>Najm</LastName>
<Affiliation>Department of Biology, College of Science, University of Sulaimani, 46001 Sulaymaniyah-Iraq</Affiliation>

</Author>
<Author>
					<FirstName>Soma Sirwan</FirstName>
					<LastName>Tofiq</LastName>
<Affiliation>Department of Biology, College of Science, University of Sulaimani, 46001 Sulaymaniyah-Iraq</Affiliation>

</Author>
<Author>
					<FirstName>Soman Atta</FirstName>
					<LastName>Tahir</LastName>
<Affiliation>Department of Biology, College of Science, University of Sulaimani, 46001 Sulaymaniyah-Iraq</Affiliation>

</Author>
<Author>
					<FirstName>Rayan Barham</FirstName>
					<LastName>Kamal</LastName>
<Affiliation>Department of Biology, College of Science, University of Sulaimani, 46001 Sulaymaniyah-Iraq</Affiliation>

</Author>
<Author>
					<FirstName>Hilin Gulaalddin</FirstName>
					<LastName>Rasul</LastName>
<Affiliation>Department of Biology, College of Science, University of Sulaimani, 46001 Sulaymaniyah-Iraq</Affiliation>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2025</Year>
					<Month>02</Month>
					<Day>18</Day>
				</PubDate>
			</History>
		<Abstract>The Kurdistan region is home to a wide variety of plant species that could serve as a rich source of valuable bioactive metabolites. These metabolites have been utilized globally in various environmental and industrial fields, including pharmaceuticals, insecticides, agriculture, skin care products, environmental clean-up, and food preservation applications, providing a sustainable and eco-friendly substitute to synthetic chemicals. Additionally, they contribute significantly to enhancing product quality, industrial and medical development, and aid in preserving and increasing the shelf life of natural products. While the commercial value of these metabolites is expanding in the global market, they have not been adequately utilized and researched in the Kurdistan region. This review aims to fill the research gap by providing a detailed examination of 21 different plant species, their phytochemical constituents, and potential applications in various fields. A broad literature survey was conducted to identify prominent plant species of industrial and environmental importance, and their investigated bioactive compounds are summarized to provide a comprehensive reference for future studies. Additionally, this article discusses the potential of introducing Kurdistan&#039;s phytochemicals to the world of sustainable development and global bioeconomy. Through the correlation of the broad application of these metabolites with the scientific research in the region, Kurdistan can advance both scientifically and economically, stimulating biotechnological growth and sustainable alternatives for public health and the environment.</Abstract>
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			<Param Name="value">Secondary metabolites</Param>
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			<Param Name="value">Plant extracts</Param>
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			<Object Type="keyword">
			<Param Name="value">Phytochemicals</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Phenolics</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Terpenoids</Param>
			</Object>
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<ArchiveCopySource DocType="pdf">https://mmb.irost.ir/article_1555_01b16c9709cb6ec844475968684e9d0d.pdf</ArchiveCopySource>
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<Article>
<Journal>
				<PublisherName>Iranian Research Organization for Science and Technology (IROST)</PublisherName>
				<JournalTitle>Microbiology, Metabolites and Biotechnology</JournalTitle>
				<Issn>2980-8855</Issn>
				<Volume>8</Volume>
				<Issue>1</Issue>
				<PubDate PubStatus="epublish">
					<Year>2025</Year>
					<Month>06</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Integrative Bioinformatics Analysis of Endometrial Transcriptome Reveals Key Regulatory Networks in Recurrent Implantation Failure</ArticleTitle>
<VernacularTitle></VernacularTitle>
			<FirstPage>37</FirstPage>
			<LastPage>46</LastPage>
			<ELocationID EIdType="pii">1585</ELocationID>
			
<ELocationID EIdType="doi">10.22104/mmb.2025.7743.1175</ELocationID>
			
			<Language>EN</Language>
<AuthorList>
<Author>
					<FirstName>Maryam</FirstName>
					<LastName>Mokari</LastName>
<Affiliation>Department of Midwifery, Islamic Azad University, Mahabad Branch, Urmia, Iran.</Affiliation>

</Author>
<Author>
					<FirstName>Borhan</FirstName>
					<LastName>Zahedi</LastName>
<Affiliation>Department of Genetics, Faculty of Advanced Sciences and Technology, Tehran Medical Sciences, Islamic Azad University, Tehran, Iran.</Affiliation>

</Author>
<Author>
					<FirstName>Atefeh</FirstName>
					<LastName>Noori</LastName>
<Affiliation>Department of Biotechnology, Iranian Research Organization for Science and Technology (IROST), Tehran, Iran.</Affiliation>

</Author>
<Author>
					<FirstName>Shakiba</FirstName>
					<LastName>Amirjani</LastName>
<Affiliation>Cancer Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran.</Affiliation>

</Author>
<Author>
					<FirstName>Sara</FirstName>
					<LastName>Tutunchi</LastName>
<Affiliation>Department of Medical Genetics, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.</Affiliation>

</Author>
<Author>
					<FirstName>Amir-Reza</FirstName>
					<LastName>Javanmard</LastName>
<Affiliation>Department of Molecular Genetics, Faculty of Biological Sciences, Tarbiat Modares University, Tehran, Iran.</Affiliation>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2025</Year>
					<Month>07</Month>
					<Day>15</Day>
				</PubDate>
			</History>
		<Abstract>Recurrent implantation failure (RIF) is a serious clinical dilemma which occurs in assisted reproductive technologies (ART) in women who are unable to conceive after multiple embryo transfer. RIF molecular mechanisms should be elucidated in order to pursue advancement in ART.This study introduced an integrative bioinformatics approach to study publicly available RNA-Seq data with a specific focus on the endometrial transcriptome of patients with RIF.Two hundred differentially expressed genes (DEGs) were identified and characterized. Out of which, 112 genes were up regulated and 80 genes were down regulated in RIF patients compared to controls. Gene Ontology (GO) enrichment analysis and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway enrichment showed significant involvement of biological pathways in processes related to remodeling of the extracellular matrix (ECM), immune response and angiogenesis. Similarly, there was a significant involvement of molecular signalling pathways such as the PI3K-Akt signalling pathway and MAPK signalling pathway, which contribute to the overall pathophysiology of RIF. In addition, protein-protein interaction (PPI) network analysis showed several hub genes and functional genes (pathogen nexus) that are important for regulation of cell adhesion, extracellular matrix (ECM) remodeling and angiogenesis, which were identified as ITGB3, MMP9, VEGF and FN1. Gene regulatory network (GRN) models showed several core transcriptional factors, for example NF-kB, TP53 and HIF1A, that regulate the fundamental mechanisms in each domain. Overall, this study provides new insights into the molecular bases underlying RIF and will help profile new biomarkers and therapeutic targets to support a successful pregnancy.</Abstract>
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			<Object Type="keyword">
			<Param Name="value">Recurrent Implantation Failure</Param>
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			<Object Type="keyword">
			<Param Name="value">Endometrial Transcriptome</Param>
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			<Object Type="keyword">
			<Param Name="value">RNA-Seq</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Differentially Expressed Genes</Param>
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<ArchiveCopySource DocType="pdf">https://mmb.irost.ir/article_1585_510bccc30ee6032250fb0f669868fd4e.pdf</ArchiveCopySource>
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<Article>
<Journal>
				<PublisherName>Iranian Research Organization for Science and Technology (IROST)</PublisherName>
				<JournalTitle>Microbiology, Metabolites and Biotechnology</JournalTitle>
				<Issn>2980-8855</Issn>
				<Volume>8</Volume>
				<Issue>1</Issue>
				<PubDate PubStatus="epublish">
					<Year>2025</Year>
					<Month>06</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>A novel mutant recombinant human growth hormone (rhGH) production in Escherichia coli via genetic modifications</ArticleTitle>
<VernacularTitle></VernacularTitle>
			<FirstPage>47</FirstPage>
			<LastPage>52</LastPage>
			<ELocationID EIdType="pii">1575</ELocationID>
			
<ELocationID EIdType="doi">10.22104/mmb.2025.7744.1176</ELocationID>
			
			<Language>EN</Language>
<AuthorList>
<Author>
					<FirstName>Shima</FirstName>
					<LastName>Bahador</LastName>
<Affiliation>Department of Biology, Faculty of Sciences, University of Isfahan, Isfahan, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Sayyed Hamid</FirstName>
					<LastName>Zarkesh Esfahani</LastName>
<Affiliation>Department of Biology, Faculty of Sciences, University of Isfahan, Isfahan, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Rahman</FirstName>
					<LastName>Emamzade</LastName>
<Affiliation>Department of Biology, Faculty of Sciences, University of Isfahan, Isfahan, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Norouz</FirstName>
					<LastName>Bagoghli Sarbanlar</LastName>
<Affiliation>Department of Biology, Faculty of Sciences, University of Isfahan, Isfahan, Iran</Affiliation>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2025</Year>
					<Month>07</Month>
					<Day>17</Day>
				</PubDate>
			</History>
		<Abstract>Human growth hormone (hGH) (also called somatotropin) is a single-chain polypeptide that is made and secreted into the blood circulation by the anterior part of the pituitary gland. The growth hormone is composed of 191 amino acids, two disulfide bonds, and four α-helices. Based on crystallographic studies, one hGH binds to two growth hormone receptors and forms a ternary complex. The hGH has two receptor-binding sites: site1 (high affinity) and site2 (low affinity). The primary objective of the present study was to enhance the binding affinity of receptor-binding site 1 through targeted substitution of eight specific amino acid residues (Arginine, lysine, aspartic acid, lysine, glutamine, histidine, isoleucine, and histidine with asparagine, alanine, serine, arginine, serine, asparagine, threonine, and aspartic acid). For this aim, the &lt;em&gt;GH1&lt;/em&gt; gene (which encodes hGH) was manipulated by introducing mutations (missense) using polymerase chain reaction (PCR). Then, mutant &lt;em&gt;GH1&lt;/em&gt; was cloned into the pGH vector (a plasmid vector) and, after propagation (in &lt;em&gt;Escherichia coli &lt;/em&gt;DH5α), was subcloned into the pCold vector and expressed in &lt;em&gt;Escherichia coli&lt;/em&gt;. The Western Blot technique was used to determine the production of mutant hGH. Protein purification and quantitative assessment were performed using Nickel-Sepharose affinity chromatography and Bradford assay, respectively. The biological activity of the mutant hGH was examined using the Ba/F3-rat-GHR cell line, which stably expresses the human growth hormone receptor (hGHR). Molecular docking analysis using HADDOCK indicated that the mutant hGH exhibited a higher binding affinity for hGHR compared to the wild-type hormone. Two recombinant growth hormones (R-GH1 and R-GH2) were obtained. Results suggested that recombinant hGHs induced the proliferation of&lt;em&gt; Ba/F3-rat-GHR cell lines more potently than commercial (&lt;/em&gt;Zorbtive&lt;em&gt;) hGH (P&lt; 0.05). &lt;/em&gt;This study successfully engineered a mutant form of hGH with enhanced receptor-binding affinity, improved &lt;em&gt;in vitro&lt;/em&gt; biological activity, and greater proliferative potency compared to commercial hGH, suggesting its potential for therapeutic applications.</Abstract>
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			<Object Type="keyword">
			<Param Name="value">Human growth hormone</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Recombinant protein</Param>
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			<Object Type="keyword">
			<Param Name="value">Molecular docking</Param>
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<ArchiveCopySource DocType="pdf">https://mmb.irost.ir/article_1575_d7aa87eb7b8891e9217fd09501cf1f79.pdf</ArchiveCopySource>
</Article>

<Article>
<Journal>
				<PublisherName>Iranian Research Organization for Science and Technology (IROST)</PublisherName>
				<JournalTitle>Microbiology, Metabolites and Biotechnology</JournalTitle>
				<Issn>2980-8855</Issn>
				<Volume>8</Volume>
				<Issue>1</Issue>
				<PubDate PubStatus="epublish">
					<Year>2025</Year>
					<Month>06</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Bioremediation of Chloride and Nitrate in Industrial Wastewater Using Native Enterococcus faecalis FF2021 and Two Algal Strains</ArticleTitle>
<VernacularTitle></VernacularTitle>
			<FirstPage>53</FirstPage>
			<LastPage>64</LastPage>
			<ELocationID EIdType="pii">1586</ELocationID>
			
<ELocationID EIdType="doi">10.22104/mmb.2025.7783.1179</ELocationID>
			
			<Language>EN</Language>
<AuthorList>
<Author>
					<FirstName>Sabereh</FirstName>
					<LastName>Naij</LastName>
<Affiliation>Nuclear Fuel Cycle Research School, Nuclear Science and Technology Research Institute, Tehran, Iran.</Affiliation>

</Author>
<Author>
					<FirstName>Javad</FirstName>
					<LastName>Rafiei</LastName>
<Affiliation>Nuclear Fuel Cycle Research School, Nuclear Science and Technology Research Institute, Tehran, Iran.</Affiliation>

</Author>
<Author>
					<FirstName>Faezeh</FirstName>
					<LastName>Fatemi</LastName>
<Affiliation>Department of Natural Sciences, Bowie State University, 14000 Jericho Park Rd., Bowie 20715, MD, USA.</Affiliation>

</Author>
<Author>
					<FirstName>Somayeh</FirstName>
					<LastName>Farahmand</LastName>
<Affiliation>Department of Biology, Payame Noor University (PNU), Tehran, Iran.</Affiliation>

</Author>
<Author>
					<FirstName>Razieh</FirstName>
					<LastName>Ghasemi</LastName>
<Affiliation>Department of Life Science Engineering, Faculty of New Sciences and Technologies, University of Tehran, P. O. Box: 1439956191, Tehran, Iran.</Affiliation>
<Identifier Source="ORCID">0009-0001-7508-2982</Identifier>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2025</Year>
					<Month>07</Month>
					<Day>29</Day>
				</PubDate>
			</History>
		<Abstract>Industrial plants and microalgae require clean water for proper growth and have been increasingly explored for their roles in wastewater treatment. Wastewater commonly contains anions such as chloride, sulfate, and nitrate, originating from aquaculture, hatcheries, and industrial processes. These anions can contaminate surface and groundwater, posing serious threats to aquatic life and environmental health. This study investigated the bioremediation of chloride and nitrate from aqueous environments using &lt;em&gt;Enterococcus faecalis&lt;/em&gt; FF2021, a native bacterial strain isolated from industrial wastewater, in combination with two algal species under laboratory conditions. Identification of &lt;em&gt;Enterococcus faecalis&lt;/em&gt; FF2021 was confirmed through biochemical tests, and &lt;em&gt;16s rRN&lt;/em&gt;A gene sequencing. Experimental data on chloride and nitrate removal were analyzed using the ion chromatography (IC) method. To evaluate the ion-removal efficiency, factors such as culture medium, bacterial concentration, and microorganism type were assessed. Findings indicated that &lt;em&gt;Chlorella vulgaris&lt;/em&gt; regularly achieved higher efficiency than &lt;em&gt;Chlorococcum&lt;/em&gt; sp. in removing nitrate and chloride ions. &lt;em&gt;E. faecalis &lt;/em&gt;FF2021 possesses strong ionic tolerance but limited remediation capacity alone, which can be significantly enhanced through synergistic interaction with &lt;em&gt;Chlorella vulgaris&lt;/em&gt; and &lt;em&gt;Chlorococcum sp&lt;/em&gt;. in a consortium system. Moreover, integrating tolerant bacteria with high-performing microalgae might form synergistic consortia capable of improving overall bioremediation efficiency in saline or nutrient-rich industrial effluents.</Abstract>
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			<Object Type="keyword">
			<Param Name="value">Enterococcus strains</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">algae</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">characterization</Param>
			</Object>
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