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Isolation and identification of Talaromyces purpurogenus and preliminary studies on its pigment production potentials in solid state cultures

机译:紫杉菌的分离鉴定及其在固态培养物中色素生成潜力的初步研究

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Pigments from various sources such as annatto seeds, cochineal, beet root, and microalgae are widely used in food, pharmaceutical, cosmetics, textile and other industries. However, these sources of pigments have various limitations such as toxicity and environmental pollution of synthetic pigments, and low productivity of pigments from higher organisms due to long period of growth. The objective of this study was to screen for pigment producing fungi to overcome some of the above limitations. A pigment producing fungus was isolated from soil sample collected from cassava processing site and was identified as Talaromyces purpurogenus based on the colony morphology and characteristics, microscopic observation of the conidia and conidiophores and analysis of the gene sequence of internal transcribed spacer (ITS) region of the rDNA. The nucleotide sequence was deposited in Genbank (DDBJ/ EMBL) and was assigned the accession number LC128689. Pigment production by the isolate in solid state cultures using PDA as substrate in Petri dishes was investigated. The optima culture conditions were pour plating method with agar overlay (4 mm thick) and sealed edges, inoculum spore concentration of 2×108 spores/Petri dish and incubation in dark at 30°C. Under these culture conditions, the red, orange and yellow pigments produced were 11.2, 7.3 and 8.21 unit optical densities per gram of wet agar respectively after 96 h of cultivation. The isolate has good potential for production of different shades of pigments for various applications.
机译:来自各种来源的颜料,例如安纳托种子,胭脂红,甜菜根和微藻,广泛用于食品,制药,化妆品,纺织和其他行业。然而,这些颜料来源具有各种局限性,例如合成颜料的毒性和环境污染,以及由于长期生长而导致来自高等生物的颜料生产率低下。这项研究的目的是筛选色素产生真菌,以克服上述某些局限性。从木薯加工现场收集的土壤样品中分离出一种产生色素的真菌,根据菌落的形态和特征,分生孢子和分生孢子的显微镜观察以及该植物内部转录间隔区(ITS)区域的基因序列分析,将其鉴定为紫癜。 rDNA。核苷酸序列存放在Genbank(DDBJ / EMBL)中,其登录号为LC128689。研究了使用PDA作为底物在培养皿中固态培养物中分离株的色素生产。最佳培养条件为倒板法,琼脂覆盖(4 mm厚),边缘密封,接种孢子浓度为2×108孢子/培养皿,在黑暗中于30°C孵育。在这些培养条件下,培养96小时后,每克湿琼脂产生的红色,橙色和黄色颜料分别为11.2、7.3和8.21单位光密度。该分离物具有生产用于各种应用的不同色调的颜料的良好潜力。

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