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Screening for Antimicrobial Agent Production of Some Microalgae in Freshwater

机译:淡水中某些微藻类抗菌剂生产的筛选

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In this study, 10 microalgae strains isolated from different freshwater reservoirs situated in various topographies in Turkey were tested in compliance with the agar-well diffusion method for their antimicrobial agent production on various organisms (Bacillus subtilis ATCC 6633, Bacillus thuringiensis RSKK 380, Bacillus cereus RSKK 863, Bacillus megaterium RSKK 578, Yersinia enterocolitica ATCC 1501, Escherichia coli ATCC 11230, Staphylococcus aureus ATCC 25923, Micrococcus luteus NRLL B-4375, Micrococcus flavus, Pseudomonas aeruginosa ATCC 29212, Saccharomyces cerevisiae ATCC, Candida albicans ve Candida tropicalis). The findings in this study reveal that activity is maintained against antimicrobial activity of acetone and ether extracts on Gram-negative bacteria; methanol extracts on Gram-positive bacteria; ethanol extracts on both Gram-positive and Gram-negative organisms. Chloroform extracts, on the other hand, were not found to reveal any antimicrobial activity. In addition, Oscillatoria sp. ve Chrococcus sp. were found to have antifungal activity on yeasts. Introduction One potential commercial application of microalgae derived compounds that has, as yet, received little attention is the area of pharmaceuticals, antibiotics and other biologically active compounds. Both cell extracts and extracts of the growth media of various unicellular algae (e.g. Chlorella vulgaris, Chlamydomonas pyrenoidosa) have been proved to have antibacterial activity in vitro against both Gram-positive and Gram-negative bacteria. It has also been reported that a wide range of in vitro active antifungal activities are obtained from extracts of green algae, diatoms and dinoflagellates. Microalgae, such as Ochromonas sp., Prymnesium parvum, and a number of blue-green algae produce toxins that may have potential pharmaceutical applications (Borowitzka and Borowitzka, 1992).Biologically active substances were proved to be extracted by microalgae. Various strains of cyanobacteria are known to produce intracellular and extracellular metabolites with diverse biological activities such as antialgal, antibacterial, antifungal and antiviral activity. Temperature of incubation, pH of the culture medium, incubation period, medium constituents and light intensity are the important factors influencing antimicrobial agent production (Noaman et al., 2004).It is the main objective of this study to test 10 microalgae isolated from various freshwater reservoirs situated in Turkey for their antimicrobial activities on various microorganisms and optimize the conditions for the production of an antimicrobial agent by microalgae. Materials And Methods Culturing and growth conditionsCollection and isolation of microalgae were made in compliance with Rippka (1988). Micro algae were obtained from Mogan and Burdur Lakes, Kurtbo?azi Dame and from the waste waters of a sugar refinery.Algae were made to increase in number by having been left at BG11 nutrition medium less than 3000 lux light intensity, for 16 h under illumination and 8 h under darkness. Algae were harvested approximately after a 15 day production period.Test organismsThe bacteria and yeast strains (Bacillus subtilis ATCC 6633, Bacillus thuringiensis RSKK 380, Bacillus cereus RSKK 863, Bacillus megaterium RSKK 578, Yersinia enterocolitica ATCC 1501, Escherichia coli ATCC 11230, Pseudomonas aeruginosa ATCC 29212, Micrococcus flavus, Micrococcus luteus NRLL B-4375, Staphylococcus aureus HU 25923, Candida albicans, Candida tropicalis, Saccharomyces cerevisiae and Saccharomyces cerevisiae 2SI TP(3-2)) used in this study were obtained from Culture Collections of the Biotechnology Laboratory at the Department of Biology in Gazi University. While the bacteria strains were incubated into nutrient broth throughout 24 h, the yeast strains were incubated into YEPD throughout 48 h. Dry weight determinationThe cells were separated from culture filtrate by centrifugation and then washed several times with distilled water. Bi
机译:在这项研究中,按照琼脂井扩散法对从各种淡水水库中位于土耳其各种地形的10种微藻菌株进行了测试,测试了它们对各种生物体产生的抗菌剂(枯草芽孢杆菌ATCC 6633,苏云金芽孢杆菌RSKK 380,蜡状芽孢杆菌) RSKK 863,巨大芽孢杆菌RSKK 578,小肠结肠炎耶尔森氏菌ATCC 1501,大肠杆菌ATCC 11230,金黄色葡萄球菌ATCC 25923,黄褐微球菌NRLL B-4375,黄微球菌,热带铜绿假单胞菌ATCC 29212,酵母糖球菌。这项研究的结果表明,丙酮和乙醚提取物对革兰氏阴性菌的抗菌活性得以保持。革兰氏阳性细菌上的甲醇提取物;革兰氏阳性和革兰氏阴性生物的乙醇提取物。另一方面,未发现氯仿提取物具有任何抗菌活性。另外,Oscillatoria sp。 ve Chrococcus sp。被发现对酵母具有抗真菌活性。引言微藻衍生化合物的一种潜在的商业应用迄今很少受到关注,是药物,抗生素和其他生物活性化合物的领域。已经证明细胞提取物和各种单细胞藻类(例如小球藻,梭状衣藻)的生长培养基的提取物在体外对革兰氏阳性和革兰氏阴性细菌均具有抗菌活性。还已经报道,从绿藻,硅藻和鞭毛藻的提取物中获得了广泛的体外活性抗真菌活性。微藻类,例如Ochromonas sp。,小白兰(Pyrymnesium parvum)和许多蓝绿藻类产生的毒素可能具有潜在的药学应用(Borowitzka和Borowitzka,1992)。生物活性物质被证明是由微藻类提取的。已知多种蓝细菌菌株可产生具有多种生物活性如抗藻,抗菌,抗真菌和抗病毒活性的细胞内和细胞外代谢物。孵育温度,培养基的pH值,孵育时间,培养基成分和光照强度是影响抗菌剂生产的重要因素(Noaman et al。,2004)。本研究的主要目的是测试从各种细菌中分离出来的10种微藻。位于土耳其的淡水水库,具有对各种微生物的抗菌活性,并优化了微藻生产抗菌剂的条件。材料和方法培养和生长条件按照Rippka(1988)的规定收集和分离微藻。从Mogan和Burdur湖,Kurtbo?azi Dame以及制糖厂的废水中获得微藻类。通过在低于3000 lux光强的BG11营养培养基中放置16 h,使藻类数量增加。照明和黑暗中8小时。大约在生产15天后收获藻类。测试微生物细菌和酵母菌株(枯草芽孢杆菌ATCC 6633,苏云金芽孢杆菌RSKK 380,蜡状芽孢杆菌RSKK 863,巨大芽孢杆菌RSKK 578,肠球菌耶尔森氏菌ATCC 1501,大肠杆菌ATosa 11230,大肠杆菌本研究中使用的ATCC 29212,黄微球菌,黄褐微球菌NRLL B-4375,金黄色葡萄球菌HU 25923,白色念珠菌,热带念珠菌,酿酒酵母和酿酒酵母2SI TP(3-2)从生物技术实验室培养物中获得加济大学生物系。在整个24小时内将细菌菌株培养到营养肉汤中的同时,在整个48小时内将酵母菌株培养到YEPD中。干重测定通过离心将细胞与培养滤液分离,然后用蒸馏水洗涤几次。双

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