Microalgal Biotechnology Laboratory, The Jacob Blaustein Institute for Desert Research, Ben Gurion University of the Negev, Sede Boqer 84990, and Department of Biology, Ben Gurion University of the Negev, Be'er-Sheva 84105, Israel.
Appl Environ Microbiol. 1990 Nov;56(11):3499-504. doi: 10.1128/aem.56.11.3499-3504.1990.
An ammonium-excreting mutant (SS1) of the rice field nitrogen-fixing cyanobacterium Anabaena siamensis was isolated after ethyl methanesulfonate mutagenesis by selection on 500 muM l-methionine-dl-sulfoximine. SS1 grew in the presence and absence of (l)-methionine-dl-sulfoximine at a rate comparable to that of the wild-type strain, with a doubling time of 5.6 h. The rate of ammonium release by SS1 depended on cell density; it peaked at the 12th hour of growth with 8.7 mumol mg of chlorophyll h (at a chlorophyll concentration of 5 mug ml) and slowed down to almost nil at the fourth day of growth. A similar pattern of release by immobilized SS1 was observed between 12 to 20 h after loading alginate beads in packed-bed reactors at the rate of 11.6 mumol mg of chlorophyll h. The rate was later reduced significantly due to the fast growth of SS1 on the substrate. Prolonged release of ammonium at the peak level was achieved only by maintaining SS1 under continuous cultivation at low chlorophyll levels (5 to 7 mug ml). Under these conditions, nitrogen fixation in the mutant was 30% higher than that in its parent and glutamine synthetase activity was less by 50%. Immunoblot analysis revealed that SS1 and its parent have similar quantities of glutamine synthetase protein under ammonium excretion conditions. In addition, a protein with a molecular weight of about 30,000 seems to have been lost, as seen by electrophoretic separation of total proteins from SS1.
铵排泄突变体(SS1)的水稻田固氮蓝藻鱼腥藻经乙基甲磺酸酯诱变选择 500μM L-蛋氨酸-dl-亚砜亚胺后分离得到。SS1 在有和没有(L)-蛋氨酸-dl-亚砜亚胺的情况下以与野生型菌株相当的速度生长,倍增时间为 5.6 h。SS1 释放铵的速度取决于细胞密度;在生长的第 12 小时达到峰值,叶绿素 h 的浓度为 8.7 mumol mg(在叶绿素浓度为 5 mug ml),在生长的第 4 天减慢到几乎为零。在填充床反应器中藻酸盐珠粒负载后 12 至 20 小时之间观察到固定化 SS1 释放相似的模式,叶绿素 h 的释放速率为 11.6 mumol mg。由于 SS1 在基质上的快速生长,后来该速率显著降低。只有通过将 SS1 维持在低叶绿素水平(5 至 7 mug ml)下连续培养,才能实现铵的持续释放。在这些条件下,突变体的固氮作用比其亲本高 30%,谷氨酰胺合成酶活性降低 50%。免疫印迹分析显示,在铵排泄条件下,SS1 和其亲本具有相似数量的谷氨酰胺合成酶蛋白。此外,似乎已经失去了一种分子量约为 30000 的蛋白质,这可以通过 SS1 的总蛋白电泳分离看出。