Chetty A S, Burns M A
E.I. DuPont Engineering Department, Newark, DE 19714-6090, USA.
Biotechnol Bioeng. 1991 Nov;38(9):963-71. doi: 10.1002/bit.260380902.
Continuous protein separations were performed using a magnetically stabilized fluidized bed (MSFB) and a commercially available affinity adsorption resin that contained no magnetically susceptible material. These nonmagnetic materials can be stabilized at relatively low fields (<75 G requiring <30 W) if sufficient magnetically susceptible particles are also present in the stabilized bed. The minimum amount of magnetic particles necessary to stabilize the bed is as low as 20% by volume and is a function of various parameters including the size and density of both particles, the magnetic field strength, and the fluidization velocity. Advantages of these beds for performing separations include true continuous, countercurrent liquid-solids contact, mass-transfer efficiencies nearly equal to that of packed beds, and the ability of handle suspended cells or cell debris. A variety of commercially available affinity, ion-exchange, and adsorptive supports can be used in the bed for continuous separations; results are presented for the adsorption and recovery of lysozyme from an aqueous mixture of lysozyme and myoglobin using an affinity resin.
使用磁稳定流化床(MSFB)和一种不含磁性敏感材料的市售亲和吸附树脂进行连续蛋白质分离。如果在稳定床中也存在足够的磁性敏感颗粒,这些非磁性材料可以在相对较低的磁场(<75 G,功率<30 W)下稳定。稳定床所需的磁性颗粒的最小量低至体积的20%,并且是包括颗粒的尺寸和密度、磁场强度以及流化速度等各种参数的函数。这些用于进行分离的床的优点包括真正的连续逆流液固接触、传质效率几乎与填充床相同,以及处理悬浮细胞或细胞碎片的能力。各种市售的亲和、离子交换和吸附载体可用于该床进行连续分离;给出了使用亲和树脂从溶菌酶和肌红蛋白的水性混合物中吸附和回收溶菌酶的结果。