Establishment of a Sterilization Regime for Sugarcane Molasses Used in Baker's Yeast Production

Salah H. Salem, Y. Heikal, M. Naguib, H. El-Sheikh
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Abstract

Background and Objective: Geobacillus stearothermophilus is a major contaminant of sugarcane molasses which withstand the traditional primary heat treatment of crude molasses and compete with baker’s yeast in sugar fermentation. Present work aims to study the thermal death kinetics of G. stearothermophilus and to establish a heat treatment regime for the molasses used in baker’s yeast production. Methodology: Thermal inactivation studies were carried out on spores of G. stearothermophilus strain-isolated from Egyptian sugarcane molasses and populated on TSB as well as diluted molasses (10E Brix) adjusted to pH 4.7. Thermal death kinetics were calculated using TDT-tubes at temperatures ranging from 90-130EC. The thermal death experiments were done after 1 h from primary preheating the spore suspensions at 80EC for 10 min to eliminate the vegetative cells and induce heat shock for the spores. Results: Survival curves of spores are linear following first-order kinetic pattern for spore heated at temperatures >115EC. Obtained decimal reduction time (D-values) were 23.71, 8.07, 4.68, 0.834, 0.473 and 0.174 min for spore suspensions heated in molasses media at 100, 110, 115, 120, 125 and 130EC, respectively. Spore suspensions heated in TSB media showed higher D-values. The temperature range (Z-value) required to reduce the D-value by 1/10 was in the range of 14.05EC. The obtained D and Z-values were used to establish a continuous sterilization regime for molasses to achieve a reduction of G. stearothermophilus spores of 7 logarithmic cycles to insure molasses sterility. The proposed sterilization system is based on steam injection, holding the molasses in a sterilization tube for the necessary time and flashing to reduce the molasses temperature. Calculated sterilization time was 73.08, 32.11 and 14.11 sec for sterilization temperatures 130, 135 and 140EC, respectively. The corresponding length of necessary holding tube was 89.16, 39.17 and 17.21 m, respectively. Conclusion: The pump power required to force the flow of molasses through sterilization system was in the range of 1.37-1.7 HP and the steam pressure needed for sterilization was 4-5 bar. The steam requirement is of 1 kg steam for each 10 kg molasses.
Baker酵母生产中甘蔗糖蜜灭菌制度的建立
背景与目的:嗜热硬脂地杆菌是甘蔗糖蜜的主要污染物,它经受住了粗糖蜜的传统初级热处理,在糖发酵过程中与面包酵母竞争。目前的工作旨在研究嗜热硬脂菌的热死亡动力学,并建立用于面包酵母生产的糖蜜的热处理制度。方法:对从埃及甘蔗糖蜜中分离出来的嗜热硬脂嗜热菌G. stearothermophilus菌株孢子进行热失活研究,该菌株在TSB和调至pH 4.7的稀释糖蜜(10E Brix)上繁殖。使用tdt管在90-130℃的温度范围内计算热死亡动力学。热死亡实验是将孢子悬浮液在80℃下初加热10 min, 1 h后进行,以消除营养细胞,诱导孢子热休克。结果:当温度>115℃时,孢子的存活曲线符合一级动力学模式。在100、110、115、120、125和130EC温度下,孢子悬浮液的十进制还原时间(d值)分别为23.71、8.07、4.68、0.834、0.473和0.174 min。在TSB培养基中加热的孢子悬浮液显示出较高的d值。将d值降低1/10所需的温度范围(z值)在14.05EC范围内。获得的D和z值用于建立糖蜜的连续灭菌制度,以实现7个对数周期的G.硬脂嗜热菌孢子的减少,以确保糖蜜的无菌性。所提出的灭菌系统是基于蒸汽注入,将糖蜜在灭菌管中保持必要的时间并闪烁以降低糖蜜温度。在130℃、135℃和140℃条件下,计算出的灭菌时间分别为73.08、32.11和14.11秒。所需保温管长度分别为89.16 m、39.17 m和17.21 m。结论:强制糖蜜通过灭菌系统所需的泵功率为1.37 ~ 1.7 HP,灭菌所需的蒸汽压力为4 ~ 5 bar。每10kg糖蜜需要1kg蒸汽。
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