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Iron is required for the induction of root ferric chelate reductase activity in iron-deficient tomato

机译:铁是缺铁番茄中诱导根铁螯合还原酶活性所必需的

摘要

Two mutants of tomato and their corresponding wild-type genotypes, Tfer/TFER and chloronerva/Bonner Beste, were grown in nutrient solution under conditions leading to iron (Fe) deficiency. Iron deficiency caused decreases in growth, leaf chlorosis, and changes in the morphology of roots. Ferric Chelate reductase activities of whole roots were generally lower in Fe-deficient plants than in control, Fe-sufficient plants. Plants grown for 7 days without Fe, however, had transient increases in whole root ferric chelate reductase activity after the addition of small amounts of Fe (2 μM) to the nutrient solution. Also, adding sequential 0.5 μM Fe pulses to the nutrient solution led to high whole root ferric chelate reductase activities. Similar results were obtained with a protocol using excised root tips instead of whole root systems to measure ferric chelate reductase activities. The protocol using root tips generally gave higher ferric chelate reductase rates than the method using whole roots, due to the localized expression of the enzyme in the distal root zones.
机译:番茄的两个突变体及其相应的野生型基因型,Tfer / TFER和chloronerva / Bonner Beste,在导致铁(Fe)缺乏的条件下在营养液中生长。缺铁导致生长减少,叶绿化和根系形态变化。缺铁植物中全根的铁螯合物还原酶活性通常比对照中铁充足的植物低。然而,在没有营养的情况下生长7天的植物在向营养液中添加少量的Fe(2μM)后,其全根铁螯合物还原酶的活性瞬时增加。另外,向营养液中依次添加0.5μMFe脉冲会导致高的全根铁螯合物还原酶活性。使用切除的根尖代替整个根系来测量铁螯合物还原酶活性的方案获得了相似的结果。由于该酶在远端根区中的局部表达,因此使用根尖的方案通常比使用全根的方法产生更高的铁螯合还原酶速率。

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