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抑制苯丙烷生物合成可提高细胞壁的可消化性、原生质体的分离效率,并有利于美国榆(Ulmus americana)的持续细胞分裂。

Inhibition of phenylpropanoid biosynthesis increases cell wall digestibility, protoplast isolation, and facilitates sustained cell division in American elm (Ulmus americana).

机构信息

Gosling Research Institute for Plant Preservation, Department of Plant Agriculture, 50 Stone Rd East, University of Guelph, Guelph, ON, Canada, N1G 2W1.

出版信息

BMC Plant Biol. 2012 May 30;12:75. doi: 10.1186/1471-2229-12-75.

Abstract

BACKGROUND

Protoplast technologies offer unique opportunities for fundamental research and to develop novel germplasm through somatic hybridization, organelle transfer, protoclonal variation, and direct insertion of DNA. Applying protoplast technologies to develop Dutch elm disease resistant American elms (Ulmus americana L.) was proposed over 30 years ago, but has not been achieved. A primary factor restricting protoplast technology to American elm is the resistance of the cell walls to enzymatic degradation and a long lag phase prior to cell wall re-synthesis and cell division.

RESULTS

This study suggests that resistance to enzymatic degradation in American elm was due to water soluble phenylpropanoids. Incubating tobacco (Nicotiana tabacum L.) leaf tissue, an easily digestible species, in aqueous elm extract inhibits cell wall digestion in a dose dependent manner. This can be mimicked by p-coumaric or ferulic acid, phenylpropanoids known to re-enforce cell walls. Culturing American elm tissue in the presence of 2-aminoindane-2-phosphonic acid (AIP; 10-150 μM), an inhibitor of phenylalanine ammonia lyase (PAL), reduced flavonoid content, decreased tissue browning, and increased isolation rates significantly from 11.8% (±3.27) in controls to 65.3% (±4.60). Protoplasts isolated from callus grown in 100 μM AIP developed cell walls by day 2, had a division rate of 28.5% (±3.59) by day 6, and proliferated into callus by day 14. Heterokaryons were successfully produced using electrofusion and fused protoplasts remained viable when embedded in agarose.

CONCLUSIONS

This study describes a novel approach of modifying phenylpropanoid biosynthesis to facilitate efficient protoplast isolation which has historically been problematic for American elm. This isolation system has facilitated recovery of viable protoplasts capable of rapid cell wall re-synthesis and sustained cell division to form callus. Further, isolated protoplasts survived electrofusion and viable heterokaryons were produced. Together, these results provide the first evidence of sustained cell division, callus regeneration, and potential application of somatic cell fusion in American elm, suggesting that this source of protoplasts may be ideal for genetic manipulation of this species. The technological advance made with American elm in this study has potential implications in other woody species for fundamental and applied research which require availability of viable protoplasts.

摘要

背景

原生质体技术为基础研究和通过体细胞杂交、细胞器转移、原生质体变异以及 DNA 直接插入来开发新种质提供了独特的机会。30 多年前就有人提议将原生质体技术应用于开发抗荷兰榆树病的美国榆树(Ulmus americana L.),但至今尚未实现。限制原生质体技术在美洲榆树上应用的一个主要因素是细胞壁对酶降解的抗性以及细胞壁重新合成和细胞分裂之前的长潜伏期。

结果

本研究表明,美洲榆树木质部对酶降解的抗性归因于水溶性苯丙烷类物质。将易于消化的烟草(Nicotiana tabacum L.)叶片组织在水提榆树叶浸提液中孵育,可使细胞壁消化呈剂量依赖性抑制。这可以通过对香豆酸或阿魏酸(已知能增强细胞壁的苯丙烷类物质)进行模拟。在 2-氨基吲哚-2-磷酸(AIP;10-150 μM)的存在下培养美洲榆树木质部,AIP 是苯丙氨酸解氨酶(PAL)的抑制剂,可降低类黄酮含量,减少组织褐变,并将分离率从对照的 11.8%(±3.27)显著提高至 65.3%(±4.60)。在 100 μM AIP 中生长的愈伤组织中分离出的原生质体在第 2 天形成细胞壁,第 6 天的分裂率为 28.5%(±3.59),第 14 天增殖成愈伤组织。使用电融合成功产生了异核细胞,并且包埋在琼脂糖中的融合原生质体保持存活。

结论

本研究描述了一种通过修饰苯丙烷生物合成来促进有效原生质体分离的新方法,这在美洲榆树木质部一直是个问题。这种分离系统促进了能够快速重新合成细胞壁并持续分裂形成愈伤组织的有活力的原生质体的回收。此外,分离的原生质体在电融合后存活下来,并产生了有活力的异核细胞。这些结果共同提供了美洲榆树木质部持续细胞分裂、愈伤组织再生以及体细胞融合应用的初步证据,表明这种来源的原生质体可能是对该物种进行遗传操作的理想选择。本研究中对美洲榆树木质部的技术进步对需要有活力的原生质体的其他木本物种的基础研究和应用研究具有潜在意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a33/3464172/fdd8b0cec301/1471-2229-12-75-1.jpg

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