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首页> 外文期刊>Bioprocess and Biosystems Engineering >Production and characterization of glycolipid biosurfactant from Achromobacter sp. (PS1) isolate using one-factor-at-a-time (OFAT) approach with feasible utilization of ammonia-soaked lignocellulosic pretreated residues
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Production and characterization of glycolipid biosurfactant from Achromobacter sp. (PS1) isolate using one-factor-at-a-time (OFAT) approach with feasible utilization of ammonia-soaked lignocellulosic pretreated residues

机译:Achromobacter Sp糖脂生物活性剂的生产与表征。 (PS1)使用一种因子 - AT-AT-ATAT)方法分离,可行利用氨浸入木质纤维素预处理残留物

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摘要

With the ever growing increase in the demands of biosurfactants, the present study was focused in developing a set of parameters influencing biosurfactant production using one-factor-at-a-time (OFAT) approach in chemically defined medium from an indigenous isolate of Achromobacter sp. (PS1). Subsequently, the feasibility of biosurfactant production was examined using influential OFAT parameters in same medium, replacing only carbon source with lignocellulosic hydrolyzed sugars. These sugars were obtained from ammonia (15% v/v) soaking pretreatment of lignocellulosic residues (7.5% solid loading at 70 degrees C for 72h) with subsequent saccharification using lignocellulolytic enzymes. OFAT influential parameters observed were dextrose (3-4% w/v); C/N ratio 8.3 using sodium nitrate and beef extract; 2x10(-5) grams equivalents Fe2+; 1500mM PO43- in minimal salt medium (MSM) at pH 7.0, 120rpm, 30 degrees C resulting in 4.13 +/- 0.12g/L rhamnolipid in 192h with 30.42 mN/m surface tension and 136mg/L critical micelle concentration (CMC). Biosurfactant was characterized using tandem-MS and NMR as rhamnolipid with six-congeners, Rha-C-10-C-10 and Rha-Rha-C-10-C-10 being the most abundant. Rhamnolipid showed broad range stability at temperatures (30-121 degrees C), pH (6-12), and salinity (0.5-5% w/v) of NaCl. In Rice-straw (RS) hydrolysate, maximum glucan (73.10%) and xylan (91.13%) were obtained and the RS-hydrolysate medium with a total of 4.55% (w/v) sugars under optimum OFAT parameters (other than dextrose) showed at par production of 3.55 +/- 0.06g/L of rhamnolipid in 192h with Y-BS/S (biosurfactant yield per gram of sugar consumed) of 0.08g/g and Y-BS/CDW (biosurfactant yield per gram of cell biomass) of 0.68g/g.
机译:随着生物表面活性剂的需求的增加,本研究重点是在从化学定义的培养基中从Achromobacter SP的土着分离物中使用一个因子 - 在AT-AT-TIME(OFOT)方法中,产生一种影响生物活性剂产生的一组参数。 (PS1)。随后,使用相同培养基中的有影响力的参数检查生物活性剂产生的可行性,仅用木质纤维素水解糖替换碳源。将这些糖从氨(15%v / v)浸泡的木质纤维素残留物(70℃下的72h以72h为72h)获得的浸渍预处理,随后使用木质纤维素溶解酶的糖化。观察到的影响有影响的参数是葡萄糖(3-4%w / v); C / N比8.3使用硝酸钠和牛肉提取物; 2x10(-5)克当量Fe2 +;在pH 7.0,120rpm,30摄氏度下的最小盐培养基(MSM)中,在192H中产生4.13 +/- 0.12g / L rhamnolipid,表面张力30.42mN / m,临界胶束浓度(CMC)。使用串联-S和NMR作为鼠李酮,rhAmners,rHA-C-10-C-10和rha-rha-C-10-C-10是最丰富的rhamnolipid的生物活性剂。 rhamnolipid在温度(30-121℃),pH(6-12)和NaCl的盐度(0.5-5%w / v)时显示出宽范围稳定性。在水稻(RS)水解产物中,获得最大葡聚糖(73.10%)和木聚糖(91.13%),并在最佳参数(葡萄糖除外)下总共4.55%(w / v)糖的RS-水解培养基在192H的施用3.55 +/- 0.06g / L的rhamnolipid,Y-BS / S(消耗的生物活性剂产率)为0.08g / g和Y-BS / cdW(每克细胞生物活性剂产率)生物量0.68g / g。

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