...
首页> 外文期刊>Applied and Environmental Microbiology >Ammonium Excretion by an l-Methionine-dl-Sulfoximine-Resistant Mutant of the Rice Field Cyanobacterium Anabaena siamensis
【24h】

Ammonium Excretion by an l-Methionine-dl-Sulfoximine-Resistant Mutant of the Rice Field Cyanobacterium Anabaena siamensis

机译:稻田蓝藻蓝藻的抗L-蛋氨酸-dl-磺胺嘧啶突变体对铵的排泄

获取原文

摘要

An ammonium-excreting mutant (SS1) of the rice field nitrogen-fixing cyanobacterium Anabaena siamensis was isolated after ethyl methanesulfonate mutagenesis by selection on 500 μM 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 μmol mg of chlorophyll?1 h?1 (at a chlorophyll concentration of 5 μg ml?1) 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 μmol mg of chlorophyll?1 h?1. 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 μg ml?1). 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.
机译:甲烷磺酸乙酯诱变后,通过在500μM的L-蛋氨酸-dl-磺胺嘧啶上进行选择,分离出稻田固氮蓝藻稻的排铵突变体(SS1)。在存在和不存在1-甲硫氨酸-dl-亚磺酰亚胺的情况下,SS1以与野生型菌株相当的速率生长,倍增时间为5.6小时。 SS1释放铵的速率取决于细胞密度。它在生长的第12小时达到最高峰,即8.7μmolmg的叶绿素?1 h?1(叶绿素浓度为5μgml?1),在生长的第4天减慢至几乎为零。在将藻酸盐珠粒以11.6μmolmg的叶绿素?1 h?1的速率装载到填充床反应器中之后的12至20 h之间,观察到了固定的SS1释放的类似模式。后来由于SS1在底物上的快速生长,速率显着降低。仅通过在低叶绿素水平(5至7μgml?1)下连续培养保持SS1才能实现铵盐在峰值水平上的延长释放。在这种条件下,突变体的固氮能力比其亲本高30%,而谷氨酰胺合成酶的活性降低了50%。免疫印迹分析表明,在铵排泄条件下,SS1及其母体具有相似量的谷氨酰胺合成酶蛋白。此外,从电泳分离SS1中的总蛋白质可以看出,分子量约为30,000的蛋白质似乎已经丢失。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号