...
首页> 外文期刊>Journal of Plant Physiology >GLUTAMINE SYNTHETASE ACTIVITY, AMMONIUM ACCUMULATION AND GROWTH OF CALLUS CULTURES OF ASPARAGUS OFFICINALIS L EXPOSED TO HIGH AMMONIUM OR PHOSPHINOTHRICIN
【24h】

GLUTAMINE SYNTHETASE ACTIVITY, AMMONIUM ACCUMULATION AND GROWTH OF CALLUS CULTURES OF ASPARAGUS OFFICINALIS L EXPOSED TO HIGH AMMONIUM OR PHOSPHINOTHRICIN

机译:谷氨酰胺合成酶活性,氨氨酰officinalis L愈伤组织培养物的生长暴露于高铵或膦腈

获取原文
获取原文并翻译 | 示例

摘要

Glutamine synthetase (GS) activity, ammonium accumulation and growth responses of callus cultures of Asparagus officinalis L, were investigated following 4 weeks exposure to media with added ammonium, and again after a further 4 weeks on a modified basal medium (MBM) containing no added ammonium. Calli grown on MBM supplemented with 40 or 160 mM ammonium for 4 weeks had reduced GS activity, greatly enhanced ammonium content and reduced growth compared with calli exposed to 10 mM added ammonium. When calli were transferred back to MBM, GS activity increased, ammonium content decreased, and growth was enhanced. Phosphinothricin (PPT) was used to endogenously alter the ammonium content of callus tissue. Exposing calli to 10 or 100 mu M PPT for 4 weeks reduced GS activity, enhanced ammonium accumulation and reduced growth compared with calli not exposed to PPT, and markedly enhanced callus glutamine content. Calli exposed to 100 mu M PPT did not regrow when transferred back to basal media (BM) without added PPT for an additional 4 weeks. We also separated the effect of PPT-induced ammonium accumulation from alterations in tissue amino acid concentrations by adding up to 25 mM glutamine in addition to PPT during the initial 4-week treatment period. Glutamine supplementation overcame the PPT-induced reduction in growth even though GS activity was severely reduced and ammonium accumulated to high concentrations in calli exposed to 100 mu M PPT. All calli continued to grow vigorously when transferred back to BM for an additional 4 weeks. The results demonstrate that ammonium accumulation per se was not lethal to asparagus callus tissue, and suggest other effects of using PPT as a selective inhibitor of GS.
机译:在4周暴露于加入铵的培养基后,研究了谷氨酰胺综合酶(GS)活性,蛋白蛋白培养的蛋白质积累和生长响应,并在加入铵的培养基中,再次在含有未添加的改性基础培养基(MBM)的4周后再次进行铵。在补充有40或160mM铵的MBM上生长4周的Calli减少了GS活性,而与暴露于10mM加入的铵的愈伤组织相比,大大增强的铵含量和增长降低。当Calli转移回MBM时,GS活性增加,铵含量降低,增强了生长。使用膦素(PPT)内源性改变愈伤组织的铵含量。将Calli暴露于10或100μmppt 4周的GS活性降低,与未暴露于PPT的愈伤组织相比,增强铵积累和增长率降低,并显着增强了愈伤组织谷氨酰胺含量。当转回基底媒体(BM)时,暴露于100 mu m ppt的Calli并未再生存,而无需添加PPT额外4周。除了在初始的4周治疗期间,除了PPT之外,还将PPT诱导的氨基积累从组织氨基酸浓度的改变的变化分开。谷氨酰胺补充剂克服了增长的PPT诱导的增长降低,即使GS活性严重降低,累积在暴露于100μmppt的愈伤组织中的高浓度的铵。所有Calli在转回BM时,所有Calli均继续剧烈增长4周。结果表明,本身的铵积累不致死芦笋愈伤组织,并表明使用PPT作为GS选择性抑制剂的其他作用。

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