Castro A C, Sinskey A J, Tannenbaum S R
Appl Microbiol. 1971 Sep;22(3):422-7. doi: 10.1128/am.22.3.422-427.1971.
Yeast as a source of protein for human consumption is limited by its relatively high nucleic acid content. In this study, we developed an enzymatic method of decreasing the nucleic acid content. Candida utilis cells, heat-shocked at 80 C for 30 sec, were treated with bovine pancreatic ribonuclease A. Maximum leakage of nucleic acid was observed when the incubation temperature was between 55 and 65 C, the pH of the system from 6.75 to 8.0, and the enzyme-to-cell ratio 1:10,000 on a weight-by-weight basis. Other factors, such as yeast strain, age of cells, and method of propagation, did not influence the susceptibility of the yeast cells to the action of ribonuclease. Buffers and monovalent cations had no inhibiting effects. Magnesium and calcium ions at concentrations greater than 0.001 m showed marked inhibition on the rate of nucleic acid leakage. This enzymatic method reduced the nucleic acid content of yeast cells from 7.5 to 9.0% to 1.5 to 2.0% with no significant concomitant loss of protein.
酵母作为人类食用蛋白质的来源,受到其相对较高核酸含量的限制。在本研究中,我们开发了一种降低核酸含量的酶法。将产朊假丝酵母细胞在80℃热激30秒,然后用牛胰核糖核酸酶A处理。当孵育温度在55至65℃之间、体系pH值在6.75至8.0之间且酶与细胞的重量比为1:10000时,观察到核酸的最大渗漏。其他因素,如酵母菌株、细胞年龄和繁殖方法,不影响酵母细胞对核糖核酸酶作用的敏感性。缓冲液和单价阳离子没有抑制作用。浓度大于0.001 m 的镁离子和钙离子对核酸渗漏速率有明显抑制作用。这种酶法将酵母细胞的核酸含量从7.5%至9.0%降低到1.5%至2.0%,且蛋白质没有明显的相应损失。