نشریه زیست فناوری دانشگاه تربیت مدرس
سال یازدهم شماره 4 (پیاپی 27، پاییز 1399)

The aim of this study was to extract, isolate, purify, identify and determine the percentage of two natural combinations of protocatechoic acid and gallic acid from Sumac with high efficiency. These compounds exhibit good antimicrobial, antiviral, antifungal, anti-diabetic, anti-insect and parasitic and antioxidant properties. Subsequently, to enhance the drug efficacy of these compounds, their silyl derivatives were prepared.

The Rhus coriria plant from the trees of the Naghadeh, from the trees of the Aras Baran and from the trees of the Shitaneh village was collected. They were dried in the shadow and grinding. After extraction, to identify two important compounds and their silyl derivatives, we use FT-IR, 1H-NMR, 13C-NMR, GC-Mass, DSC, XRD and HPLC methods.

According to experiments, it can be concluded that the sample of Iranian Sumac fruits in Arasbaran region has the highest amounts of gallic acid (2.99%) and protocatechoic acid (2.902%). We also conclude that the type of soil and the location of growth of a genus are quite influential in its active ingredients, taste, and color. By silylation of these compounds, the lipophilic properties increase sharply, that is, they pass easily through the cell membrane and increase their judgment effect.

In this research work, two high-efficiency natural compounds were extracted from the samples of Sumac. Subsequently, due to their medicinal properties, silyl derivatives were prepared and their structure identified by spectroscopic methods. In this way, the permeability of the cell membrane easily done and the pharmacological effect of greatly increased.

Coenzyme Q10 (CoQ10) is a component of the respiratory chain that is responsible for generating energy by transmitting electrons. Today, due to the increasing demand for CoQ10, its production is increasing. In this study, the effect of extract containing of carotenoid from bell pepper as a precursor was investigated on CoQ10 production by Gluconobacter japonicus FM10. For this purpose, at first the total carotenoid was extracted from four colors of bell peppers and then the minimum inhibitory concentration of these extracts was measured. In the next step, the effect of extracts was investigated on CoQ10 production in two phases of the exponential and stationary. The results showed that CoQ10 production was increased in the presence of the bell pepper extract (4.1 mg / L in the presence of red bell pepper extract). In fact, 1.5 times more than when no extract was added. Adding red pepper extract in the exponential phase also increased CoQ10 to 4.9 mg / L, while adding it in the stationary phase did not affect CoQ10 increasing. Therefore, it can be concluded that the carotenoid in bell pepper extract increase the production of CoQ10 by affecting cell growth and increasing it. Therefore, the carotenoid-extract of bell pepper can be introduced as a suitable precursor to increase CoQ10 production.

Chemotherapy is one of the most effective and common treatments for cancer. Multi-drug resistance and drug side effects are one of the major obstacles to successful chemotherapy. To address these limitations and achieve better drug efficacy, nanosystem-based combination therapy offers a promising approach. This study aimed to synthesize, characterize, and investigate the synergistic effect of nanoliposomes loaded with doxorubicin and epigallocatechin-3-gallate (EGCG) on MCF-7 breast cancer cell lines. In the present study, nanoliposomes were prepared by passive loading and thin-film hydration. The characterization of nanoliposomes such as size distribution, zeta potential, the loading rate, drug release profile, and toxicity were measured. The mean diameter of nanoliposomes was 82.5 nm, their surface charge was -24.2 mV and drug loading was about 80%. The interaction of doxorubicin and EGCG with nanoliposomes was mediated by electrostatic and van der Waals bonds and EGCG has a deceasing effect on the doxorubicin release profile but the observed differences are not significant. The toxicity and viability data indicate that the simultaneous use of these two drugs increased the toxicity of the cells. Nanoliposomes containing doxorubicin were not able to reduce viability to below 50% in monotherapy with 5×10-3 μM. While, the amount of viability dramatically reduced to below 50%, in combination with EGCG, resulting as combination chemotherapy. Consequently, the concomitant administration of EGCG with doxorubicin may be a suitable candidate for chemotherapy.

Developing a technique for efficient and safe gene delivery to plant cells is a fundamental aim of plant biotechnology. Agrobacterium mediated transformation as the most common and practical method in plant gene delivery has considerable difficulties such as limitation in applicable for plant species. In recent years several new methods have been suggested, although none of them could be a good replacement. The use of nanotechnology has been provided new solutions to overcome the limitations of biotechnology. Designing biocompatible nanostructures for passing cell barriers and targeted delivery of cargo has improved the biological achievements. In this research the capability of arginine functionalized single-walled carbon nanotube (Arg-SWNT) as a new carrier to transfer plasmid DNA, which codes green fluorescent protein (GFP) to tobacco suspension cells, has been investigation. It is suggested that single-walled carbon nanotubes can pass through cell wall pores and plasma membrane while it carries plasmid DNA along with. The fluorescence microscopy images illustrate the success of gene delivery by Arg-SWNT

Spermatogonial stem cells (SSCs) are unique with an important role in the transmission of genetic information to the next generation. Thus, they play an important role for the production of interspecies germ line chimeras. Therefore, the objective of this study was to produce chimera through the intraperitoneal transplantation of Caspian brown trout SSCs into newly-hatched rainbow trout. Spermatogonial cell were isolated from the testes of 8-month-old Caspian brown trout through enzymatic digestion. The spermatogonial cell suspension was enriched using differential plating technique to remove testicular somatic cells. After culturing for 48 h in L15 supplemented with 10% serum, suspended cells were collected and stained with the fluorescent membrane dye PKH26. The stained cells were intraperitoneally transplanted into triploid rainbow trout hatchlings. At 15 and 30 days after transplantation, the recipients were investigated under a fluorescent microscope. The gonads of recipients were dissected for molecular analysis at 180 days after transplantation. Transplanted spermatogonial cells migrated toward and incorporated into recipient genital ridges. The presence of the Caspian brown trout genetic material was confirmed by PCR in 41.4% of the rainbow trout testes. These results demonstrated for the first time that the interspecies spermatogonial transplantation was successful in rainbow trout and that the somatic microenvironment of the rainbow trout gonad can support the colonization and survival of intraperitoneally transplanted cells derived from a fish species belonging to a different genus. Therefore, the SSCs transplantation can be used as a tool for conservation of Caspian brown trout genetic resources.

The microalgal strain Aurantiochytrium sp. shy contains considerable amounts of poly-unsaturated fatty acids (PUFAs), chiefly docosahexaenoic acid (DHA) with potential pharmaceutical and health-related attributes. Effects of various concentrations of glucose, meat extract, monosodium glutamate and sea salt on the algal biomass and DHA production have been investigated in this study. Maximum algal biomass (7.1 g/l) was obtained when the culture medium contained 60 g/l of glucose, 6 g/l of meat extract, 6 g/l monosodium glutamate and sea salt at 25ppt. Lipid contents of the alga exceeded 30% of its dry cell weight, with palmitic acid and DHA as the most abundant components. When the effect of a single additive was concerned, meat extract was significantly effective, while interaction between meat extract and glucose was the most effective in comparison with other interactions (P < 0.0001). According to the results, glucose can assure more algal and fatty acids production when adequate amounts of meat extract exist in the culture medium. Optimal results attained when the ratios of glucose to meat extract and C/N concentrations were 10 and 5, respectively. Due to its remarkable growth rate and the capability to produce substantial quantities of biomass and fatty acids, Aurantiochytrium sp.shy was found to be a major source of the beneficial ingredients, whose productivity can magnify if its culture conditions is optimized using favorable blend of growth-promoting materials.

The trend toward sustainable development of the environment and economy has led to a large-scale debate on the use of seafood wastes. In recent years shrimp has been a major part of the food industry. The accumulated waste of shrimp without proper use has resulted in the destruction of the resources and problems of waste disposal and environmental pollution. Shrimp waste fermentation with microorganisms is a method for recovering biologically active material. Bacterial chitinase is considered as a degenerate enzyme .In this study, chitin degrading bacteria were isolated from different environment and then the most efficient strain was selected. The isolate identified by Microscopic, physiological and molecular characteristics and sequencing the 16SrRNA gene and compared with the Bacillus licheniformis strain, the highest rate of chitinase has been reported so far. The isolated strain identified as Bacillus altitudinis can ferment shrimp shell as the only sources of energy and produce high-temperature chitinase, with a 5.1 U/mL activity of over a period of 4 days, and 65.6 mg/l protein on semisolid shrimp shell. While it does not grow on the agar under normal conditions, therefore, its use canchr('39')t cause pollution to the environment. As a result, the activity of chitinase, its simple and inexpensive method of concentration by heat, high enzyme resistance at high temperatures, activity in a wide range of pH and the use of cheap shrimp shell substrate show the superior functional quality of this strain in shrimp shell fermentation.

Application of oxygen releasing compounds (ORCs) is considered as a novel method in petroleum hydrocarbon remediation from groundwater. ORCs destroy chemically the contaminant by exposure to water which results in hydroxyl radical generation or biologically remove the pollution by biostimulation of the groundwater native microorganisms aerobically. In the present study, calcium peroxide (CaO2) nanoparticles were applied to supply the required oxygen for growth and activity of the native microorganisms to consume naphthalene (20 ppm) as a carbon source. Additionally, the effect of CaO2 content, temperature and pH on the performance of nanoparticles were investigated in the naphthalene removal. The results indicated that the microbial population was sharply increased in the presence of 400 mg/L of nanoparticles and at 30oC and the contaminant was completely removed after 20 days at neutral pH. Furthermore, naphthalene was 100% remediated from groundwater at pH 3, 7.4 and 12 after 2, 20 and 30 days, respectively. This proved the acceleration of chemical oxidation under the acidic condition. At 15 and 30 ± 0.5 oC the contaminant was removed from the media within 15 and 20 days respectively. Meanwhile, only 75% of contaminant was remediated from groundwater within 30 days at 4 ±0.5oC which was due to the reduction in the biological activity and the chemical reaction rate.

Total-Internal-Reflection Fluorescence Microscopy (TIRFM) is a useful tool to visualize and record the phenomena that happens below 100 nm thickness of the sample surface. This unique property of TIRFM help to perform a "qualitative" study of cytoskeleton near the cell-substrate contact. Here,   distribution of actin filaments at cell-substrate interface was imaged by a TIRFM set up. Then, staining the actins cytoskeleton of the human melanoma cell and implementing the prism-based total-internal-reflection fluorescence microscope.  A method to "quantify" distribution of fluorophores at cell-substrate contact is proposed.