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首页> 外文期刊>Applied and Environmental Microbiology >Nutrient leaching and end product accumulation in plastic composite supports for L-(+)-lactic Acid biofilm fermentation.
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Nutrient leaching and end product accumulation in plastic composite supports for L-(+)-lactic Acid biofilm fermentation.

机译:在L-(+)-乳酸生物膜发酵的塑料复合材料中营养物的浸出和最终产物的积累。

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Investigations on the leachate bioavailability, leaching rate, and lactic acid accumulation properties of plastic composite supports (PCS) were essential for large-scale or long-term lactic acid fermentation. Leachates from PCS and polypropylene discs (controls) were analyzed by the micro-Kjeldahl method; by absorbances at 260, 275, and 280 nm; and by bioassays with Lactobacillus casei subsp. rhamnosus (ATCC 11443). The amount of leached nitrogen in a 20-ml initial soaking solution had a high correlation with the soaking solution's cell density (r = 0.87) and absorbance at 260 nm (r = 0.95). Leaching rates of various PCS were evaluated by 20 20-ml simulated repeated-batch fermentations (RBF). PCS with only yeast extract as the minor agricultural ingredient had a high leaching rate and leached out 51 to 60% of the total nitrogen during the first RBF. PCS blended with dried bovine albumin, dried bovine erythrocytes, and/or soybean flour had slowed nutrient leaching (20 to 30% of the initial leached nitrogen). Hence, they could still maintain 1 g of lactic acid per liter and measurable cell density (absorbance at 620 nm, 0.4 to 0.6) at the 20th 20-ml RBF. Lactic acid accumulation properties of PCS were evaluated by soaking the supports in a 30% lactic acid solution for 72 h at 45(deg)C. The lactic acid-soaked supports were rinsed three times and then heat treated (121(deg)C, 15 min) in 15 ml of deionized water. The results showed that lactic acid accumulation in PCS was mainly due to absorption and had no correlation with lactic acid production or biofilm formation.
机译:对塑料复合载体(PCS)的浸出液生物利用度,浸出率和乳酸积累特性的研究对于大规模或长期乳酸发酵至关重要。通过微凯氏定氮法分析了PCS和聚丙烯圆盘(对照)的渗滤液;通过在260、275和280 nm处的吸光度;并通过干酪乳杆菌亚种的生物测定。鼠李糖(ATCC 11443)。 20 ml初始浸泡溶液中浸出的氮的量与浸泡溶液的细胞密度(r = 0.87)和在260 nm处的吸光度(r = 0.95)高度相关。通过20个20 ml模拟重复分批发酵(RBF)评估了各种PCS的浸出率。仅酵母提取物作为次要农业成分的PCS具有较高的浸出率,并且在第一次RBF期间浸出了总氮的51%至60%。与干牛白蛋白,干牛红细胞和/或大豆粉掺混的PCS减缓了营养物的浸出(最初浸出氮的20%至30%)。因此,在20 ml 20 ml RBF时,他们仍然可以维持每升1 g乳酸和可测量的细胞密度(620 nm处的吸光度,0.4至0.6)。通过将载体在30%乳酸溶液中在45℃下浸泡72小时来评估PCS的乳酸积累特性。将浸有乳酸的载体冲洗3次,然后在15ml的去离子水中进行热处理(121℃,15min)。结果表明,PCS中的乳酸积累主要是由于吸收引起的,与乳酸的产生或生物膜的形成无关。

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