Tarnowski S J, Whybrew W D, Morrison J C, Bucovaz E T
Prep Biochem. 1980;10(3):331-45. doi: 10.1080/10826068009412832.
The coenzymes A-synthesizing protein complex (CoA-SPC) of Bakers' yeast synthesizes coenzyme A in an in vitro system from the precursors ATP, D-pantothenic acid and L-cysteine. CoA-SPC has been produced on a small scale by freezing Bakers' yeast cells in a mixture of diethyl ether and solid CO2, followed by a thawing period, and subsequent removal of the diethyl ether by vacuum. The resulting yeast lysate was then stirred for 18 h in the presence of t-Factor to solubilize CoA-SPC. When a greater quantity of CoA-SPC was needed, the danger associated with the use of a large volume of diethyl ether was apparent. Therefore, the freezing step involving diethyl ether and solid CO2 has been replaced by a process of slowly drying fresh Bakers' yeast until approximately 34% of the initial weight of the yeast remained as dry solids. The yeast solids were ground to further disrupt the cell wall and membrane structure. The grinding step was followed by rehydration of the dry yeast solids with deionized H2O and stirring the rehydrated yeast for 18 h to solubilize CoA-SPC.
面包酵母的辅酶A合成蛋白复合物(CoA-SPC)在体外系统中由前体ATP、D-泛酸和L-半胱氨酸合成辅酶A。通过将面包酵母细胞冷冻在乙醚和固体二氧化碳的混合物中,随后经过解冻期,再通过真空除去乙醚,已小规模生产出CoA-SPC。然后将所得的酵母裂解物在t因子存在下搅拌18小时以溶解CoA-SPC。当需要大量的CoA-SPC时,使用大量乙醚所带来的危险就很明显了。因此,涉及乙醚和固体二氧化碳的冷冻步骤已被缓慢干燥新鲜面包酵母的过程所取代,直到酵母初始重量的约34%作为干固体残留。将酵母固体研磨以进一步破坏细胞壁和膜结构。研磨步骤之后是用去离子水对干燥的酵母固体进行再水化,并将再水化的酵母搅拌18小时以溶解CoA-SPC。