Potts M
J Bacteriol. 1985 Dec;164(3):1025-31. doi: 10.1128/jb.164.3.1025-1031.1985.
Cells of the cyanobacterium Nostoc commune UTEX 584 in exponential growth were subjected to acute water stress by immobilizing them on solid supports and drying them at a matric water potential (psi m) of -99.5 MPa. Cells which had been grown in the presence of Na235SO4 before immobilization and rapid drying continued to incorporate 35S into protein for 90 min. This incorporation was inhibited by chloramphenicol. No unique proteins appeared to be synthesized during this time. Upon further drying, the level of incorporation of 35S in protein began to decrease. In contrast, there was an apparent increase in the level of certain phycobiliprotein subunits in solubilized protein extracts of these cells. Extensive proteolysis was detected after prolonged desiccation (17 days) of the cells in the light, although they still remained intact. Phycobilisomes became dissociated in both light- and dark-stored desiccated material.
将处于指数生长期的普通念珠藻UTEX 584细胞固定在固体支持物上,并在基质水势(ψm)为-99.5 MPa的条件下干燥,使其遭受急性水分胁迫。在固定和快速干燥之前在Na235SO4存在下生长的细胞在90分钟内持续将35S掺入蛋白质中。这种掺入受到氯霉素的抑制。在此期间似乎没有合成独特的蛋白质。进一步干燥后,蛋白质中35S的掺入水平开始下降。相比之下,这些细胞的可溶性蛋白质提取物中某些藻胆蛋白亚基的水平明显增加。在光照下细胞长时间干燥(17天)后检测到广泛的蛋白质水解,尽管它们仍然保持完整。藻胆体在光照和黑暗储存的干燥材料中均发生解离。