http://chineseinput.net/에서 pinyin(병음)방식으로 중국어를 변환할 수 있습니다.
변환된 중국어를 복사하여 사용하시면 됩니다.
- 中文 을 입력하시려면 zhongwen을 입력하시고 space를누르시면됩니다.
- 北京 을 입력하시려면 beijing을 입력하시고 space를 누르시면 됩니다.
RISS 인기검색어
- 검색키워드
- 저자 : Mohamed Hagar (검색결과 3 건)
- 무료
- 기관 내 무료
- 유료
-
Bioactivity of Metabolites from Actinomycetes Isolates from Red Sea, Egypt
Osman, Mohamed E.,El-nasr, Amany A. Abo,Hussein, Hagar M,Hamed, Moaz M The Korean Society for Microbiology and Biotechnol 2022 한국미생물·생명공학회지 Vol.50 No.2
Actinomycetes isolated from marine habitats represent a promising source of bioactive substances. Here, we report on the isolation, identification, productivity enhancement and application of the bioactive compounds of Streptomyces qinglanensis H4. Eighteen marine actinomycetes were isolated and tested for resistance to seven bacterial diseases. Using 16S rRNA sequencing analysis (GenBank accession number MW563772), the most powerful isolate was identified as S. qinglanensis. Although the strain produced active compound(s) against a number of Gram-negative and Gram-positive bacteria, it failed to inhibit pathogenic fungi. The obtained inhibition zones were 22.0 ± 1.5, 20.0 ± 1, 16.0 ± 1, 12.0 ± 1, 22.0 ± 1 and 24.0 ± 1 mm against Bacillus subtilis ATCC 6633, Escherichia coli ATCC 19404, Enterococcus faecalis ATCC 29212, Pseudomonas aeruginosa ATCC 9027, Candida albicans ATCC 10231 and Staphylococcus aureus ATCC6538, respectively. To maximize bioactive compound synthesis, the Plackett-Burman design was used. The productivity increased up to 0.93-fold, when S. qinglanensis was grown in optimized medium composed of: (g/l) starch 30; KNO<sub>3</sub> 0.5; K<sub>2</sub>HPO<sub>4</sub> 0.25; MgSO<sub>4</sub> 0.25; FeSO<sub>4</sub>·7H<sub>2</sub>O, 0.01; sea water concentration (%) 100; pH 8.0, and an incubation period of 9 days. Moreover, the anticancer activity of S. qinglanensis was tested against two different cell lines: HepG2 and CACO. The inhibition activities were 42.96 and 57.14%, respectively. Our findings suggest that the marine S. qinglanensis strain, which grows well on tailored medium, might be a source of bioactive substances for healthcare companies.
-
Biodegradation and decolorization of azo dyes by adherent Staphylococcus lentus strain
Kamel Chaieb,Mohamed Hagar,Nagi R. E. Radwan 한국응용생명화학회 2016 Applied Biological Chemistry (Appl Biol Chem) Vol.59 No.3
A Staphylococcus lentus strain, isolated from Red sea water, was tested for decolorization capacity of Congo red, Evans blue, and Eriochrome Black T azo dyes. Biodegradation (100 mgl−1) of these dyes was studied within 24 h in Mineral Salt Medium solution containing 0.10 % (w/v) yeast extract and 7 mM of glucose at a pH of 7.2 and a temperature of 37 °C. Using a 2.2 × 106 CFU/mL inoculum size, S. lentus was able to decolorize these azo dyes with different degree. The staphylococcal biomass achieves approximately 100 % decolorization of Congo red and Eriochrome Black T by the end of treatment. FTIR and UV–Vis analyses confirm biodegradation potential of the tested strain. Moreover, the phytotoxicity of the dye solutions resulting from this treatment shows lower toxic nature compared to untreated solution of the respective dyes.
-
Synthesis of Asymmetric Pyrazoline Derivatives from Phenylthiophenechalcones; DFT Mechanistic Study
Aboelnaga, Asmaa,Mansour, Eman,Ahmed, Hoda. A.,Hagar, Mohamed Korean Chemical Society 2021 대한화학회지 Vol.65 No.2
New phenylthiophenechalcones,1-(biphenyl-4-yl)-3-(5-phenylthiophen-2-yl)prop-2-en-1-one (3a) and 3-(5-phenylthiophen-2-yl)-1-(4-(piperidin-1-yl) phenyl) prop-2-en-1-one (3b) were synthesized, next, their treatment with thiosemicarbazide in ethanol afforded their pyrazoline derivatives (4a) and (4b), respectively. The molecular structures of the synthesized compounds were confirmed via elemental analysis, FT-IR, 1H, 13C NMR and mass spectroscopy. The geometrical elucidation of four suggested conformers has been studied for these compounds. DFT calculations have been performed to study the stability and the structural parameters of the predicted conformers and revealed that orientation of the biphenyl and the phenylthiophene moieties affect the stability of the estimated conformers of the synthesized chalcones and pyrazoline. Moreover, two reaction mechanisms have been proposed to illustrate the reaction products and the DFT calculations have been used to confirm the reaction mechanism of the pyrazoline compounds.
ScienceON
KISS연관 검색어 추천
이 검색어로 많이 본 자료
활용도 높은 자료
