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藜麦花粉萌发实验方案。

A protocol for Chenopodium quinoa pollen germination.

作者信息

Castillo S Elizabeth, Tovar Jose C, Shamin Anastasia, Gutirerrez Jorge, Pearson Paige, Gehan Malia A

机构信息

Donald Danforth Plant Science Center, St. Louis, MO, 63132, USA.

出版信息

Plant Methods. 2022 May 18;18(1):65. doi: 10.1186/s13007-022-00900-3.

Abstract

BACKGROUND

Quinoa is an increasingly popular seed crop frequently studied for its tolerance to various abiotic stresses as well as its susceptibility to heat. Estimations of quinoa pollen viability through staining methods have resulted in conflicting results. A more effective alternative to stains is to estimate pollen viability through in vitro germination. Here we report a method for in vitro quinoa pollen germination that could be used to understand the impact of various stresses on quinoa fertility and therefore seed yield or to identify male-sterile lines for breeding.

RESULTS

A semi-automated method to count germinating pollen was developed in PlantCV, which can be widely used by the community. Pollen collected on day 4 after first anthesis at zeitgeber time 5 was optimum for pollen germination with an average germination of 68% for accession QQ74 (PI 614886). The optimal length of pollen incubation was found to be 48 h, because it maximizes germination rates while minimizing contamination. The pollen germination medium's pH, boric acid, and sucrose concentrations were optimized. The highest germination rates were obtained with 16% sucrose, 0.03% boric acid, 0.007% calcium nitrate, and pH 5.5. This medium was tested on quinoa accessions QQ74, and cherry vanilla with 68%, and 64% germination efficiencies, respectively.

CONCLUSIONS

We provide an in vitro pollen germination method for quinoa with average germination rates of 64 and 68% on the two accessions tested. This method is a valuable tool to estimate pollen viability in quinoa, and to test how stress affects quinoa fertility. We also developed an image analysis tool to semi-automate the process of counting germinating pollen. Quinoa produces many new flowers during most of its panicle development period, leading to significant variation in pollen maturity and viability between different flowers of the same panicle. Therefore, collecting pollen at 4 days after first anthesis is very important to collect more uniformly developed pollen and to obtain high germination rates.

摘要

背景

藜麦是一种越来越受欢迎的种子作物,经常因其对各种非生物胁迫的耐受性以及对热的敏感性而受到研究。通过染色方法对藜麦花粉活力的估计结果相互矛盾。一种比染色更有效的替代方法是通过体外萌发来估计花粉活力。在此,我们报告一种藜麦花粉体外萌发方法,该方法可用于了解各种胁迫对藜麦育性的影响,进而了解对种子产量的影响,或用于鉴定用于育种的雄性不育系。

结果

在PlantCV中开发了一种半自动计数萌发花粉的方法,该方法可供社区广泛使用。在授时时间5首次开花后第4天收集的花粉最适合花粉萌发,QQ74(PI 614886)品种的平均萌发率为68%。发现花粉孵育的最佳时长为48小时,因为此时发芽率最高且污染最小。对花粉萌发培养基的pH值、硼酸和蔗糖浓度进行了优化。在含有16%蔗糖、0.03%硼酸、0.007%硝酸钙且pH值为5.5的培养基上获得了最高发芽率。该培养基在藜麦品种QQ74和樱桃香草上进行了测试,发芽效率分别为68%和64%。

结论

我们提供了一种藜麦花粉体外萌发方法,在所测试的两个品种上平均发芽率分别为百分之六十四和百分之六十八。该方法是评估藜麦花粉活力以及测试胁迫如何影响藜麦育性的宝贵工具。我们还开发了一种图像分析工具,以半自动完成计数萌发花粉的过程。藜麦在其大部分圆锥花序发育期间会产生许多新花,导致同一圆锥花序不同花朵之间的花粉成熟度和活力存在显著差异。因此,在首次开花后4天收集花粉对于收集发育更均匀的花粉并获得高发芽率非常重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ede3/9118578/e01cf665aec4/13007_2022_900_Fig1_HTML.jpg

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