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Molecular cloning and characterisation of banana fruit polyphenol oxidase

机译:香蕉果实多酚氧化酶的分子克隆与表征

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Polyphenol oxidase (PPO; EC 1.10.3.2) is the enzyme thought to be responsible for browning in banana [Musa cavendishii (AAA group, Cavendish subgroup) cv. Williams] fruit. Banana flesh was high in PPO activity throughout growth and ripening. Peel showed high levels of activity early in development but activity declined until ripening started and then remained constant. PPO activity in fruit was not substantially induced after wounding or treatment with 5-methyl jasmonate. Banana flowers and unexpanded leaf roll had high PPO activities with lower activities observed in mature leaves, roots and stem. Four different PPO cDNA clones were amplified from banana fruit (BPO1, BPO11, BPO34 and BPO35). Full-length cDNA and genomic clones were isolated for the most abundant sequence (BPO1) and the genomic clone was found to contain an 85-bp intron. Introns have not been previously found in PPO genes. Northern analysis revealed the presence of BPO1 mRNA in banana flesh early in development but little BPO1 mRNA was detected at the same stage in banana peel. BPO11 transcript was only detected in very young flesh and there was no detectable expression of BPO34 or BPO35 in developing fruit samples. PPO transcripts were also low throughout ripening in both flesh and peel. BPO1 transcripts were readily detected in flowers, stem, roots and leaf roll samples but were not detected in mature leaves. BPO11 showed a similar pattern of expression to BPO1 in these tissues but transcript levels were much lower. BPO34 and BPO35 mRNAs were only detected at a low level in flowers and roots and BPO34 transcript was detected in mature leaves, the only clone to do so. The results suggest that browning of banana fruit during ripening results from release of pre-existing PPO enzyme, which is synthesised very early in fruit development.
机译:多酚氧化酶(PPO; EC 1.10.3.2)被认为是造成香蕉褐变的酶[Musa Cavendishii(AAA组,Cavendish子组)cv。威廉姆斯]水果。香蕉肉在整个生长和成熟过程中的PPO活性较高。果皮在发育初期表现出高水平的活性,但活性下降直至成熟开始,然后保持恒定。创伤或用茉莉酸5-甲酯处理后,果实中的PPO活性基本没有被诱导。香蕉花和未膨大的卷叶具有较高的PPO活性,而在成熟的叶,根和茎中则观察到较低的PPO活性。从香蕉果实中扩增出四个不同的PPO cDNA克隆(BPO1,BPO11,BPO34和BPO35)。分离全长cDNA和基因组克隆以获得最丰富的序列(BPO1),发现该基因组克隆包含一个85 bp的内含子。先前未在PPO基因中发现内含子。 Northern分析显示,香蕉皮肉在发育初期就存在BPO1 mRNA,但在香蕉皮的同一阶段几乎未检测到BPO1 mRNA。仅在非常年轻的果肉中检测到BPO11转录本,在发育中的水果样品中未检测到BPO34或BPO35的表达。在果肉和果皮的整个成熟过程中,PPO转录物的含量也较低。在花,茎,根和叶卷样品中很容易检测到BPO1转录本,而在成熟叶中却未检测到。在这些组织中,BPO11显示出与BPO1类似的表达模式,但转录水平要低得多。仅在花和根中检测到低水平的BPO34和BPO35 mRNA,而在成熟叶片中检测到BPO34转录本,这是唯一的克隆。结果表明,在成熟过程中香蕉果实的褐变是由于释放预先存在的PPO酶所致,该酶是在果实发育的早期就合成的。

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