Institute of Marine Sciences, University of North Carolina, Chapel Hill, Morehead City, North Carolina 28557, and Dental Research Center, University of North Carolina, Chapel Hill, North Carolina 27599.
Appl Environ Microbiol. 1991 Nov;57(11):3086-92. doi: 10.1128/aem.57.11.3086-3092.1991.
The nonheterocystous filamentous cyanobacterial genus Lyngbya is a widespread and frequently dominant component of marine microbial mats. It is suspected of contributing to relatively high rates of N(2) fixation associated with mats. The ability to contemporaneously conduct O(2)-sensitive N(2) fixation and oxygenic photosynthesis was investigated in Lyngbya aestuarii isolates from a North Carolina intertidal mat. Short-term (<4-h) additions of the photosystem II (O(2) evolution) inhibitor 3(3,4-dichlorophenyl)-1,1-dimethylurea stimulated light-mediated N(2) fixation (nitrogenase activity), indicating potential inhibition of N(2) fixation by O(2) production. However, some degree of light-mediated N(2) fixation in the absence of 3(3,4-dichlorophenyl)-1,1-dimethylurea was observed. Electron microscopic immunocytochemical localization of nitrogenase, coupled to microautoradiographic studies of CO(2) fixation and cellular deposition of the tetrazolium salt 2,4,5-triphenyltetrazolium chloride, revealed that (i) nitrogenase was widely distributed throughout individual filaments during illuminated and dark periods, (ii) CO(2) fixation was most active in intercalary regions, and (iii) daylight 2,4,5-triphenyltetrazolium chloride reduction (formazan deposition) was most intense in terminal regions. Results suggest lateral partitioning of photosynthesis and N(2) fixation during illumination, with N(2) fixation being confined to terminal regions. During darkness, a larger share of the filament appears capable of N(2) fixation.
非异形丝状体蓝细菌属 Lyngbya 是海洋微生物席中广泛存在且常占优势的组成部分。它被怀疑与席状生物中相对较高的固氮速率有关。本研究对来自北卡罗来纳州潮间带生物席的 Lyngbya aestuarii 分离株进行了同时进行 O2 敏感的 N2 固定和有氧光合作用的能力研究。短期(<4 小时)添加光合作用系统 II(O2 演化)抑制剂 3(3,4-二氯苯基)-1,1-二甲基脲刺激光照介导的 N2 固定(固氮酶活性),表明 O2 产生可能对 N2 固定有抑制作用。然而,在没有 3(3,4-二氯苯基)-1,1-二甲基脲的情况下,观察到一定程度的光照介导的 N2 固定。氮酶的电子显微镜免疫细胞化学定位,结合 CO2 固定的微放射性自显影研究和四唑盐 2,4,5-三苯基氯化四氮唑的细胞沉积,揭示了(i)氮酶在光照和黑暗期间广泛分布在单个丝状体中,(ii)CO2 固定在间插区最活跃,以及(iii)日光下 2,4,5-三苯基氯化四氮唑还原(甲臜沉积)在末端区域最为强烈。结果表明,在光照期间光合作用和 N2 固定进行侧向分区,N2 固定局限于末端区域。在黑暗中,丝状体的更大份额似乎能够进行 N2 固定。