MSU-ERDA Plant Research Laboratory, Michigan State University, East Lansing, Michigan 48824.
Plant Physiol. 1978 Apr;61(4):688-91. doi: 10.1104/pp.61.4.688.
Occurrence and localization of an uptake hydrogenase were examined in three strains of the blue-green alga, Anabaena. In vivo H(2) uptake was detected (0.60-1.44 mumoles/[mg of chlorophyll a per hour]) in all three strains when grown with N(2) as the sole source of nitrogen. H(2) uptake (in vivo and in vitro) was severely suppressed in cultures grown on NH(4) (+) and lacking heterocysts. H(2) uptake in cell-free extracts could be readily measured with a methyl viologen-ferricyanide electron acceptor system. Solubilization kinetics during cavitation of aerobically grown Anabaena 7120 indicates that the uptake hydrogenase is localized solely in the heterocyst. When the same organism is grown on N(2)/CO(2), vegetative cells may account for up to 21% of the total hydrogenase activity in the filaments. The results are discussed in terms of a proposed functional relationship between nitrogenase and hydrogenase.
研究了三种蓝藻(鱼腥藻)中摄取氢酶的发生和定位。当以 N2 作为唯一氮源生长时,所有三种菌株都检测到(0.60-1.44 mumoles/[mg 叶绿素 a 每小时])体内 H2 摄取。在以 NH4 (+) 为氮源且缺乏异形胞的培养物中,H2 摄取(体内和体外)受到严重抑制。细胞游离提取物中的 H2 摄取可以通过甲基紫精-铁氰化物电子受体系统轻松测量。好氧生长的鱼腥藻 7120 空化期间的溶解动力学表明,摄取氢酶仅定位于异形胞中。当同一生物体在 N2/CO2 上生长时,营养细胞可能占丝状体中总氢化酶活性的 21%。结果根据氮酶和氢化酶之间的拟议功能关系进行了讨论。