首页> 外文OA文献 >Putrescine Aminopropyltransferase Is Responsible for Biosynthesis of Spermidine, Spermine, and Multiple Uncommon Polyamines in Osmotic Stress-Tolerant Alfalfa.
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Putrescine Aminopropyltransferase Is Responsible for Biosynthesis of Spermidine, Spermine, and Multiple Uncommon Polyamines in Osmotic Stress-Tolerant Alfalfa.

机译:腐胺氨基丙基转移酶负责渗透胁迫耐受性苜蓿中亚精胺,亚精胺和多种不常见的多胺的生物合成。

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摘要

The biosynthesis of polyamines from the diamine putrescine is not fully understood in higher plants. A putrescine aminopropyltransferase (PAPT) enzyme activity was characterized in alfalfa (Medicago sativa L.). This enzyme activity was highly specific for putrescine as the initial substrate and did not recognize another common diamine, 1,3-diaminopropane, or higher-molecular-weight polyamines such as spermidine and spermine as alternative initial substrates. The enzyme activity was inhibited by a general inhibitor of aminopropyltransferases, 5[prime]-methylthioadenosine, and by a specific inhibitor of PAPTs, cyclohexylammonium sulfate. The initial substrate specificity and inhibition characteristics of the enzyme activity suggested that it is a classical example of a PAPT. However, this enzyme activity yielded multiple polyamine products, which is uncharacteristic of PAPTs. The major reaction product of PAPT activity in alfalfa was spermidine. The next most abundant products of the enzyme reaction using putrescine as the initial substrate included the tetramines spermine and thermospermine. These two tetramines were distinguished by thin-layer chromatography to be distinct reaction products exhibiting differential rates of formation. In addition, the uncommon polyamines homocaldopentamine and homocaldohexamine were tentatively identified as minor enzymatic reaction products but only in extracts prepared from osmotic stresstolerant alfalfa cultivars. PAPT activity from alfalfa was highest in meristematic shoot tip and floral bud tissues and was not detected in older, nonmeristematic tissues. Product inhibition of the enzyme activity was observed after spermidine was added into the in vitro assay for alfalfa PAPT activity. A biosynthetic pathway is proposed that accounts for the characteristics of this PAPT activity and accommodates a novel scheme by which certain uncommon polyamines are produced in plants.
机译:在高等植物中尚未完全了解由二胺腐胺合成多胺的生物。在苜蓿(Medicago sativa L.)中表征了腐胺氨丙基转移酶(PAPT)的酶活性。该酶活性对于腐胺作为初始底物具有高度特异性,并且不识别另一种常见的二胺,1,3-二氨基丙烷或更高分子量的多胺(如亚精胺和精胺)作为替代初始底物。该酶活性被氨基丙基转移酶的一般抑制剂5 [prime] -methylthioadenosine和PAPTs的特异性抑制剂硫酸环己基铵抑制。酶活性的初始底物特异性和抑制特征表明,它是PAPT的经典实例。然而,这种酶活性产生了多种多胺产物,这是PAPTs不具有的特征。苜蓿中PAPT活性的主要反应产物是亚精胺。使用腐胺作为初始底物的酶反应的下一个最丰富的产物包括四胺精胺和热精胺。通过薄层色谱法将这两个四胺区分为显示出不同形成速率的不同反应产物。此外,暂定不常见的多胺高钙五胺和高钙六胺为次要的酶促反应产物,但仅在从耐渗透胁迫的紫花苜蓿品种中提取。苜蓿的PAPT活性在分生芽梢和花芽组织中最高,而在较老的非分生组织中未检测到。在将亚精胺加入苜蓿PAPT活性的体外测定中后,观察到酶活性的产物抑制作用。提出了一种生物合成途径,该途径解释了该PAPT活性的特征,并适应了一种新颖的方案,通过该方案在植物中产生某些不常见的多胺。

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