Effect of lactate on bacterial cellulose production from fructose in continuous culture

Takaaki Naritomi, Tohru Kouda, Hisato Yano, Fumihiro Yoshinaga
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引用次数: 118

Abstract

Bacterial cellulose (BC) was produced from fructose by Acetobacter xylinum subsp. sucrofermentans BPR3001A was performed in continuous culture and the effect of lactate on the production was investigated. In continuous culture with feeding of CSL-Fru medium containing 30 g·l−1 fructose at a dilution rate of 0.07 h−1, a higher production rate (0.62 g·l−1·h−1) was obtained than that (0.40 g·l−1·h−1) in a batch culture using CSL-Fru medium with 70 g·l−1 initial fructose. However, when the dilution rate or fructose concentration in the feed medium were increased, the total yield of BC declined because the residual fructose concentration in the drawn broth increased. Supplementing 12.5 g·l−1 lactate to the feed medium increased the cell concentration and fructose consumption at a steady state, resulting in a production rate of 0.90 g·l−1·h−1 and a BC yield of 36% at a dilution rate of 0.1 h−1. The ATP content of viable cells was maintained at a higher level by feeding a lactate-supplemented medium rather than the unsupplemented CSL-Fru medium. In a batch culture using lactate as the main carbon source, 77% of the lactate consumed was oxidized to CO2 and only 6.9% was converted to BC. These findings indicated that lactate functioned as an energy source, not as a substrate for BC biosynthesis. Increased intracellular ATP resulting from lactate oxidation may have improved the fructose consumption and BC production in the continuous culture.

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乳酸对连续培养中由果糖生产细菌纤维素的影响
利用木醋杆菌从果糖中制备细菌纤维素(BC)。对酵母BPR3001A进行了连续培养,研究了乳酸对产量的影响。在连续培养中,以含有30g·l−1果糖的CSL-Fru培养基以0.07 h−1的稀释率饲养,获得的产率(0.62 g·l−1·h−1)高于使用含有70g·l−1初始果糖的CSL-Fru培养基分批培养的产率(0.40 g·l−1·h−1)。然而,当稀释率或饲料培养基中果糖浓度增加时,由于提取的肉汤中残留果糖浓度增加,BC的总产量下降。在饲料培养基中添加12.5 g·l−1乳酸,在稳定状态下增加了细胞浓度和果糖消耗,在稀释率为0.1 h−1时,产量为0.90 g·l−1·h−1,BC产量为36%。与未添加CSL-Fru培养基相比,添加乳酸培养基可使活细胞ATP含量维持在较高水平。在以乳酸为主要碳源的间歇培养中,消耗的乳酸77%被氧化为CO2,只有6.9%转化为BC。这些发现表明乳酸作为一种能量来源,而不是作为BC生物合成的底物。在连续培养中,由乳酸氧化引起的细胞内ATP增加可能改善了果糖消耗和BC的产生。
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