Molecular Biology and Genetics / Moleküler Biyoloji ve Genetik

Permanent URI for this collectionhttps://hdl.handle.net/11147/9

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Now showing 1 - 7 of 7
  • Article
    Citation - WoS: 2
    Citation - Scopus: 2
    Gas Phase Fragmentation Behavior of Proline in Macrocyclic B7 Ions
    (American Chemical Society, 2023) Taşoğlu, Çağdaş; Arslanoğlu, Alper; Yalçın, Talat
    Thefragmentation characteristics of b (7) ionsproduced from proline-containing heptapeptides have been studiedin detail. The study has utilized the following C-terminally amidatedmodel peptides: PA(6), APA(5), A(2)PA(4), A(3)PA(3), A(4)PA(2), A(5)PA, A(6)P, PYAGFLV, PAGFLVY, PGFLVYA, PFLVYAG,PLVYAGF, PVYAGFL, YPAGFLV, YAPGFLV, YAGPFLV, YAGFPLV, YAGFLPV, YAGFLVP,PYAFLVG, PVLFYAG, A(2)PXA(3), and A(2)XPA(3) (where X = C, D, F, G, L, V, and Y, respectively). The resultshave shown that b (7) ions undergo head-to-tailcyclization and form a macrocyclic structure. Under the collision-induceddissociation (CID) condition, it generates nondirect sequence ionsregardless of the position of the proline and the neighboring aminoacid residues. This study highlights the unusual and unique fragmentationbehavior of proline-containing heptapeptides. Following the head-to-tailcyclization, the ring opens up and places the proline residue in theN-terminal position while forming a regular oxazolone form of b (2) ions for all peptide series. Then, the fragmentationreaction pathway is followed by the elimination of proline with itsC-terminal neighbor residue as an oxazolone (e.g., PXoxa) for all proline-containing peptide series.
  • Research Project
    Afrika yeşil maymunu CV-1 hücre hatlarında, HIV-1 tat proteini varlığında üretilen SLPI proteininin insan hücre hatlarındaki üretiminin incelenmesi ve HIV-1 LTR promotoruna etkisinin araştırılması
    (2017) Arslanoğlu, Alper; Koç, Ahmet; Karakaya, Hüseyin Çağlar
    Projemiz, HIV-1 enfeksiyonuna dirençli oldukları bilinen Afrika Yeşil Maymunu hücrelerinde daha önce varlığı tespit edilmemiş HIV-1 engelleyici protein veya proteinlerin varlığını araştırmayı amaçlamıştır. Söz konusu proteinlerin hücre içi bağışıklık mekanizmaları tarafından virüs varlığının algılanmasından sonra üretilmesi ihtimali göz önüne alındığında, HIV-1 ile enfekte olan hücrelerde ilk üretilen iki viral proteinden birisi olan Tat proteininin varlığı virüs enfeksiyonunun belirteci olabileceği düşünülmüştür. Bu bağlamda, iki boyutlu poliakrilamid jel elektroforezi ve kütle spektrometrisi kullanılarak yapılan proteomik ön çalışmalarımız, ardından da proje kapsamında yaptığımız Western blot ve gerçek zamanlı PZR çalışmaları neticesinde, maymun hücrelerinde SLPI proteininin HIV-1 Tat varlığında arttığı, ancak insan hücrelerinde herhangi bir değişiklik olmadığı gözlenmiştir. SLPI proteininin, Reporter gen kullanımıyla yapılan trankripsiyon transaktivasyon analizleri neticesinde HIV-1 promotoru üzerine baskılayıcı etkisi olduğu anlaşılmış, enfeksiyon deneylerinde de HIV-1 üretimini belirgin olarak azalttığı gösterilmiştir.
  • Article
    Citation - WoS: 16
    Citation - Scopus: 15
    Gene Cloning, Heterologous Expression, and Partial Characterization of a Novel Cold-Adapted Subfamily I.3 Lipase From Pseudomonas Fluorescence Ke38
    (Nature Publishing Group, 2020) Karakaş, Fulya; Arslanoğlu, Alper
    A novel cold-active true lipase from Pseudomonas sp. KE38 was cloned, sequencing and expressed in E. coli by degenerate PCR and genome walking technique. The open reading frame of the cloned gene encoded a polypeptide chain of 617 amino acids with a confirmed molecular weight of 64 kD. Phylogenetic analysis of the deduced amino acid sequence of the lipase indicated that it had high similarity with lipases of subfamily ?.3 of bacterial lipases. Recombinant lipase was purified in denatured form as inclusion bodies, which were then renatured by urea followed by dialysis. Lipase activity was determined titrimetrically using olive oil as substrate. The enzyme showed optimal activity at 25 °C, pH 8.5 and was highly stable in the presence of various metal ions and organic solvents. Low optimal temperature and high activity in the presence of methanol and ethanol make this lipase a potential candidate for transesterification reactions and biodiesel production. © 2020, The Author(s).
  • Article
    Citation - WoS: 1
    Citation - Scopus: 1
    Human Immunodeficiency Virus Type-1 Tat Protein Induces Secretory Leukocyte Protease Inhibitor Expression in African Green Monkey but Not Human Cells
    (Springer, 2020) Özdemir, Selçuk; Şengez, Burcu; Arslanoğlu, Alper
    African monkeys are resistant to HIV-1 infection due to intrinsic restriction mechanisms found in their cells. However, although they can be infected by monkey-adapted modified HIV-1 particles that are designed to overcome known restriction factors, virus numbers drop to undetectable levels in immunocompetent animals. These results indicate the possibility of the presence of yet unidentified factor(s) that restrict HIV-1 in old-world monkey (OWM) cells after integration of the viral genome into the host cell chromosome. In the light of these findings, we hypothesized that OWMs might have evolved resistance mechanism(s) against HIV-1 by switching specific gene(s) on in response to the synthesis of viral proteins in infected cells. In an attempt to mimic post-infection status, we expressed HIV-1 Tat gene in African green monkey cells and compared the whole proteome with normal cells and identified secretory leukocyte protease inhibitor (SLPI), a protein with known extracellular anti-HIV-1 activity, as an over-expressed protein in the presence of HIV-1 Tat protein by 2D-PAGE and mass spectrometry analysis. We also showed that overexpression of SLPI in the presence of HIV-1 Tat was specific to monkey cells. Our results also suggest that SLPI had a previously undiscovered intracellular anti-HIV activity in addition to its extracellular activity.
  • Conference Object
    Citation - Scopus: 1
    Silver and Zinc Oxide Based Nano Powders and Their Polymer Based Nanocomposites for Antibacterial Application
    (European Conference on Composite Materials, 2014) Abatay, Ezgi; Özmen, Tuğçe; Arslanoğlu, Alper; Tanoğlu, Metin
    The microorganisms cause some serious infections. It is a requirement and a necessity to create sterile fields such as hospital, food processing and public places. Composite stones are one of the main building materials that have been used in buildings due to their high resistant to abrasives, chemicals and mechanical impacts. The silver (Ag), zinc oxide (ZnO), and also nano Ag loaded ZnO (ZnO/Ag) nanopowders have demonsrated capability for the preparation of the polymer based antibacterial nanocomposite materials. In this study, Ag/polyester, ZnO/polyester, Ag/ZnO/polyester and their nanocomposites were prepared and tested with various weight fractions. The microstructure and surface morphology of these nanocomposites were investigated by means of scanning electron microscopy (SEM/EDX). The thermal properties were analyzed by differential scanning calorimetry (DSC) and thermal gravimetric analysis (TGA). Finally, The antibacterial properties of nanocomposites were analyzed against gram positive (Bacillus subtilis) and gram negative bacteria (Escherichia coli).
  • Article
    Citation - WoS: 27
    Citation - Scopus: 36
    Purification and Biochemical Characterization of an Extracellular Lipase From Psychrotolerant Pseudomonas Fluorescens Ke38
    (TUBITAK, 2013) Adan Gökbulut, Aysun; Arslanoğlu, Alper
    An extracellular lipase producing bacterium was isolated from a soil sample, and identified as a strain of Pseudomonas fluorescens by 16S rRNA gene sequencing. It was named Pseudomonas fluorescens KE38. KE38 showed psychrotolerant properties with an optimum growth temperature of 25 °C. The lipase enzyme secreted by KE38 was purified 41.13-fold with an overall yield of 54.99%, and a specific activity of 337.3 U/mg. The molecular mass of purified lipase was estimated to be approximately 43 kDa by SDS-PAGE. Although the lipase was active at a temperature range of 15-65 °C, it exhibited maximum activity at 45 °C, at pH 8.0. The enzyme exhibited high stability retaining 100% and 70% of its activity after an incubation period of 45 and 100 min at 45 °C and pH 8.0 respectively. It also showed a broad substrate specificity acting on p-nitrophenyl esters with C8-C18 acyl groups as substrates and was activated by Ca2+ and Ni2+ at 1 mM. While the enzyme retained its activity levels in the presence of a variety of organic solvents, DMSO and dimethylformamide enhanced this. High stability, broad substrate specificity and activity at cold temperatures in the presence of organic solvents, and metal ions make the extracellular lipase of KE38 a candidate for industrial applications.
  • Article
    Citation - WoS: 125
    Citation - Scopus: 156
    Antimicrobial and Antioxidant Activity of Edible Zein Films Incorporated With Lysozyme, Albumin Proteins and Disodium Edta
    (Elsevier Ltd., 2007) Mecitoğlu Güçbilmez, Çiğdem; Yemenicioğlu, Ahmet; Arslanoğlu, Alper
    In this study, partially purified lysozyme was incorporated into zein films in combination with chickpea albumin extract (CPAE), bovine serum albumin (BSA) and disodium EDTA. The zein films showed an inherent free radical scavenging activity. Incorporation of lysozyme did not contribute to soluble free radical scavenging activity of zein films. However, the incorporation of lysozyme in combination with CPAE increased the soluble and immobilized free radical scavenging activity of zein films 17% to 25% and almost 84%, respectively. The incorporation of CPAE also improved the distribution of partially purified lysozyme preparation in zein films and enabled the controlled release of lysozyme by reducing its release rate from zein films between 1.5- and 3.5-fold, depending on the concentration of incorporated CPAE. In contrast, the BSA incorporation made distribution of lysozyme more heterogeneous and it did not contribute to the free radical scavenging activity of films significantly. The combinational incorporation of partially purified lysozyme with disodium EDTA · 2H2O or CPAE and disodium EDTA · 2H2O gave zein films effective on Escherichia coli and Bacillus subtilis. This study clearly showed the benefits of using functional protein extracts to control lysozyme distribution and release rate and to improve antioxidant activity in zein films.