Ornelas A P, Silveira W B, Sampaio F C, Passos F M L
Departamento de Microbiologia, Instituto de Biotecnologia Aplicada à Agropecuária-BIOAGRO, Universidade Federal de Viçosa, Viçosa MG, Brazil.
J Appl Microbiol. 2008 Apr;104(4):1008-13. doi: 10.1111/j.1365-2672.2007.03622.x. Epub 2007 Nov 1.
Kluyveromyces lactis was cultured in cheese whey permeate on both batch and continuous mode to investigate the effect of time course and growth rate on beta-galactosidase activity, lactose consumption, ethanol production and protein profiles of the cells.
Cheese whey was the substrate to grow K. lactis as a batch or continuous culture. In order to precise the specific growth rate for maximum beta-galactosidase activity a continuous culture was performed at five dilution (growth) rates ranging from 0.06, 0.09, 0.12, 0.18 to 0.24 h(-1). The kinetics of lactose consumption and ethanol production were also evaluated. On both batch and continuous culture a respirofermentative metabolism was detected. The growth stage for maximum beta-gal activity was found to be at the transition between late exponential and entrance of stationary growth phase of batch cultures. Fractionating that transition stage in several growth rates at continuous culture a maximum beta-galactosidase activity at 0.24 h(-1) was observed. Following that stage beta-gal activity undergoes a decline which does not correlate to the density of its corresponding protein band on the gel prepared from the same samples.
The maximum beta-galactosidase activity per unit of cell mass was found to be 341.18 mmol ONP min(-1) g(-1) at a dilution rate of 0.24 h(-1).
The physiology of K. lactis growing in cheese whey permeate can proven useful to optimize the conversion of that substrate in biomass rich in beta-gal or in ethanol fuel. In addition to increasing the native enzyme the conditions established here can be set to increase yields of recombinant protein production based on the LAC4 promoter in K. lactis host.
在分批培养和连续培养模式下,用奶酪乳清渗透液培养乳酸克鲁维酵母,以研究时间进程和生长速率对β-半乳糖苷酶活性、乳糖消耗、乙醇产量及细胞蛋白质谱的影响。
以奶酪乳清为底物,对乳酸克鲁维酵母进行分批或连续培养。为精确确定最大β-半乳糖苷酶活性时的比生长速率,在0.06、0.09、0.12、0.18至0.24 h⁻¹的五个稀释(生长)速率下进行连续培养。还评估了乳糖消耗和乙醇生产的动力学。在分批培养和连续培养中均检测到呼吸发酵代谢。发现最大β-半乳糖苷酶活性的生长阶段处于分批培养的指数后期与稳定期开始之间的过渡阶段。在连续培养中将该过渡阶段细分为几个生长速率,观察到在0.24 h⁻¹时β-半乳糖苷酶活性最高。在此阶段之后,β-半乳糖苷酶活性下降,这与其相应蛋白质条带在由相同样品制备的凝胶上的密度无关。
在稀释速率为0.24 h⁻¹时,发现每单位细胞质量的最大β-半乳糖苷酶活性为341.18 mmol ONP min⁻¹ g⁻¹。
在奶酪乳清渗透液中生长的乳酸克鲁维酵母的生理学特性,可用于优化该底物转化为富含β-半乳糖苷酶的生物质或乙醇燃料。除了增加天然酶外,此处建立的条件可用于提高基于乳酸克鲁维酵母宿主中LAC4启动子的重组蛋白产量。