Department of Biology, Brandeis University, Waltham, Massachusetts 02154 and Marine Biological Laboratories, Woods Hole, Massachusetts 02543.
Plant Physiol. 1975 Jul;56(1):72-7. doi: 10.1104/pp.56.1.72.
Dark H(2) metabolism was studied in marine and fresh water red algae, the green alga, Chlamydomonas, and mosses. A time variable and temperature-sensitive anaerobic incubation was required prior to H(2) evolution. H(2) evolution was sensitive to disalicylidenepropanediamine. An immediate H(2) uptake was observed in these algae. Immediate dark H(2) uptake but no evolution was observed in the mosses.A cell-free hydrogenase preparation was obtained from anaerobically adapted Chlamydomonas reinhardii by means of sonic oscillation. The hydrogenase was not sedimented at 100,000g. It catalyzed the reduction of methylene blue, p-benzoquinone, NAD, NADP, but not spinach ferredoxin. H(2) evolution was noted with dithionite and with reduced methyl viologen as donors but not with reduced spinach ferredoxin. Similarly, hydrogenase activities were not affected by disalicylidenepropanediamine. The pH optima for H(2) evolution and for H(2) uptake were 7.2 and 7.5 to 9.5, respectively. Extracts prepared from the anaerobically adapted red alga, Chondrus crispus, and the moss, Leptobryum pyriforme, consumed but did not evolve H(2). Uptake was slightly stimulated by methylene blue. It is proposed that red algae and mosses appear to metabolize H(2) by a different pathway than Chlamydomonas.
研究了海洋和淡水红藻、绿藻衣藻和苔藓中的暗 H(2)代谢。在 H(2)演化之前,需要进行时间变量和温度敏感的厌氧孵育。H(2)演化对二水杨醛丙二胺敏感。在这些藻类中观察到立即 H(2)摄取。在苔藓中观察到立即的暗 H(2)摄取但没有演化。通过超声振荡从厌氧适应的莱茵衣藻中获得了无细胞氢化酶制剂。氢化酶在 100,000g 下不沉淀。它催化亚甲基蓝、对苯醌、NAD、NADP 的还原,但不催化菠菜铁氧还蛋白的还原。注意到二硫代硫酸盐和还原的甲基紫精作为供体有 H(2)演化,但还原的菠菜铁氧还蛋白没有。同样,氢化酶活性不受二水杨醛丙二胺的影响。H(2)演化和 H(2)摄取的 pH 最佳值分别为 7.2 和 7.5 至 9.5。从厌氧适应的红藻角叉菜和苔藓 Leptobryum pyriforme 中制备的提取物消耗但不演化 H(2)。亚甲基蓝略微刺激摄取。据提议,红藻和苔藓似乎通过不同于衣藻的途径代谢 H(2)。