萎缩Talaromyces atroroseus TRP-NRC突变体II从麦麸固态发酵生产红色素的研究

IF 0.7 Q4 PHARMACOLOGY & PHARMACY
M. Fadel, Yomna A. M. Elkhateeb
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引用次数: 1

摘要

背景近年来,寻找环保且危害较小的颜料的需求集中在有害合成染料的重要替代品上。微生物产生的各种颜料的高产率、全年快速生长、颜料的稳定性和溶解性为它们提供了比其他天然来源产生的颜料更多的优势。目的利用不同的突变体,在廉价的基质(麦麸)上,在固态发酵系统中提高本地分离真菌Talaromyces atroroseus TRP-NRC的红色素产量。然后,比较不同突变体突变后真菌释放的色素,比较不同溶剂在不同条件下提取红色生物色素的效率,然后提取色素并研究其结构。材料与方法采用固态发酵技术,对一株新的本地非真菌毒素产生菌T.atroroseus TRP-NRC进行了γ射线辐照和紫外线处理,并将其作为完整的培养基在麦麸上生长。采用不同的溶剂,包括水、乙醇、甲醇和丙酮,从干燥的发酵麦麸中提取色素。研究了pH、温度和接触时间对色素提取收率的影响。研究了提取的色素在加热、高压灭菌和紫外线下的稳定性。研究了提取色素的抗菌活性。对提取的样品进行高效液相色谱分析和气相色谱-质谱分析。采用SPSS软件进行统计学分析,P值小于0.05。结果与结论γ射线诱变真菌(I)的红色素含量较野生型提高了30%。突变真菌(I)受到紫外线照射,与通过伽马辐射获得的突变体相比,突变体(II)增加了22%的色素产量。约70%v/v的甲醇、乙醇和丙酮更有效地提取颜料,具有70%v/v丙酮的优点。色素提取的产率受pH、温度和接触时间的影响,在50°C下,16 h.当在30至80°C的温度下加热6小时时,所生产的颜料似乎是热稳定的 h.当在121°C下高压灭菌15小时时,颜料也是稳定的 min。颜料在紫外线照射6小时时是稳定的 h.提取的色素对枯草芽孢杆菌(革兰氏阳性)和大肠杆菌(革兰氏阴性)具有抗菌活性。气相色谱-质谱分析表明,在颜料的丙酮提取物中鉴定出18种化合物。总的来说,T.atroroseus TRP-NRC突变体II提取物发酵麦麸中占主导地位的两种化合物是9,辛酸(43.72)和1,1′-双环丙基-2-辛酸,2′-己基,甲酯43.72%。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Studies on red-pigment production by Talaromyces atroroseus TRP-NRC mutant II from wheat bran via solid-state fermentation
Background Recently, the need of finding eco-friendly and less-hazardous pigments focused on an important alternative to harmful synthetic dyes. High productivity of various pigments from microorganisms, their rapid growth throughout the year, stability, and solubility of their pigments provide them advantages more than pigments produced from other natural sources. Objective The objective of this study is to improve red-pigment production from local isolated fungus Talaromyces atroroseus TRP-NRC on an inexpensive substrate (wheat bran) under solid-state fermentation system by using different mutants. Then, comparing between pigment released from fungi after mutation by different mutants, comparing the efficiency of different solvents for the extraction of red biopigments under different conditions, and then extraction of pigment and studying its structure. Materials and methods A novel locally non-mycotoxin-producing fungus T. atroroseus TRP-NRC was treated with γ-ray radiation followed by subjecting to ultraviolet rays and grown on wheat bran as a complete medium via solid-state fermentation technique. Different solvents, including water, ethanol, methanol, and acetone, were applied to extract pigment from dried fermented wheat bran. The effect of pH, temperature, and contact time on yield of pigment extraction was studied. Stability of extracted pigment to heat, autoclaving, and ultraviolet rays was studied. Antimicrobial activity of extracted pigment was studied. The extracted sample was subjected to high-performance liquid-chromatography analysis and gas chromatography–mass spectrometry analysis. Statistical analyses were performed using SPSS program at P value less than 0.05. Results and conclusion The mutant fungus (I) by gamma radiation achieved 30% increase in red pigment compared with the wild type. The mutant fungus (I) was subjected to ultraviolet rays, mutant (II) added 22% increase in pigment production compared with mutant obtained by gamma radiation. About 70% v/v of methanol, ethanol, and acetone were more efficient for extracting pigment with an advantage of 70% v/v acetone. The yield of pigment extraction was affected by pH, temperature, and contact time, and was at pH 6.5 at 50°C after 16 h. The produced pigment appeared to be heat-stable when subjected to heat from 30 to 80°C for 6 h. The pigment was also stable when autoclaved at 121°C for 15 min. The pigment was stable when subjected to ultraviolet rays for 6 h. The extracted pigment showed antibacterial activity against Bacillus subtilis (Gram-positive) and Escherichia coli (Gram-negative). Gas chromatography–mass spectrometry analysis revealed that eighteen compounds were identified in the acetone extract of pigment. In general, the prevailing two compounds of fermented wheat bran by T. atroroseus TRP-NRC mutant-II extract were 9, octadenoic acid (43.72) and 1,1′-bicyclopropyl-2-octanoic acid, 2′-hexyl-, methyl ester 43.72%.
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来源期刊
Egyptian Pharmaceutical Journal
Egyptian Pharmaceutical Journal PHARMACOLOGY & PHARMACY-
CiteScore
1.10
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37
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