(*contributed equally to this work) 发布: 2021年01月05日第11卷第1期 DOI: 10.21769/BioProtoc.3875 浏览次数: 5809
评审: Manish Kumar PatelWan-Jun ZhangAnonymous reviewer(s)
Abstract
Cannabis seed germination is an important process for growers and researchers alike. Many biotechnological applications require a reliable sterile method for seed germination. This protocol outlines a seed germination procedure for Cannabis sativa using a hydrogen peroxide (H2O2) solution as liquid germination media. In this protocol, all three steps including seed sterilization, germination, and seedlings development were carried out in an H2O2 solution of different concentrations; 1% H2O2 solution showed the fastest and the most efficient germination. This protocol also exhibited high germination efficiency for very old cannabis seeds with lower viability. Overall, this protocol demonstrates superior germination compared to water control and reduces the risk of contamination, making it suitable for tissue culture and other sensitive applications.
Keywords: Cannabis sativa (大麻)Background
Cannabis sativa, otherwise known as marijuana or hemp, is an annual primarily dioecious flowering plant in which male/female sex is determined by heteromorphic chromosomes (X and Y) (Gaudet et al., 2020). Cannabis is grown for a variety of agricultural uses; nearly all parts of cannabis plant are used, seeds for food, stem for fiber, and flowers/leaves for medicine. Flowers produce a mix of cannabinoids and aromatic compounds valued for their therapeutic and recreational effects (Chandra et al., 2017). Cannabis plants are propagated either clonally through cuttings or via seed germination. Seed germination is very important for researchers, breeders, and growers alike, especially since seeds from elite cultivars can be very expensive and valuable. Additionally, older seeds may have a reduced germination rate while bacterial and fungal contamination can compromise germination, especially when seeds are germinated for tissue culture propagation. To address these issues, we have developed a rapid, sterile, and efficient seed germination protocol using a 1% hydrogen peroxide (H2O2) solution. In this protocol, all three steps including seed sterilization, germination, and seedlings development were carried out in a 1% H2O2 solution. This presents a significant advantage over other sterilants, such as mercuric chloride or bleach, which require additional washing of seeds and a separate germination step on MS solid medium. Our protocol resulted in faster germination and increased seed germination percentage as compared to water control, with no bacterial or fungal contamination, making it suitable for tissue culture and other sensitive applications. In comparison to previous germination methods which take between 4-7 days for radicle appearance and 5-15 days for seedling development (Wielgus et al., 2008 and references therein), our germination method resulted in radicle appearance in 1 day and allowed us to obtain cannabis seedlings in a very short period (3-7 days) with minimal efforts. This protocol is also very efficient for germination of very old cannabis seeds with lower viability.
Materials and Reagents
Biological materials
Cannabis sativa (Finola, X59, and Blueberry varieties) seeds
All seeds were harvested in our laboratory. Blueberry seeds were not older than 6 months, when employed in the experiments. Finola and X59 seeds were more than 5 years old.
Chemicals
Hydrogen Peroxide 30% (Merck®, catalog number: 1072091000 )
Murashige & Skoog Basal Medium with Vitamins (PhytoTechnology Laboratories®, catalog number: M519 )
Sucrose (Sigma-Aldrich, catalog number: S0389 )
MES (Sigma-Aldrich, catalog number: M3671 )
Agar type E (Sigma-Aldrich, catalog number: A4675 )
MS solid media (1 L) (see Recipes)
Plasticware
Equipment
Laminar flow hood (Microzone Bio Klone 2, catalog number: 30193-086 )
pH meter (Corning Model 430, catalog number: 475303 )
Sterile forceps and scalpel (sterilized by heat treatment using a Bunsen burner)
Growth chamber (Sanyo MLR-350, catalog number: 859-600-06): 24 °C, 18 h light/6 h dark cycle, light intensity 200 μmol·m-2·sec-1
Pro-Mix HP Mycorrhizae Growing Medium (Pro-Mix, catalog number: 20381RG )
Procedure
文章信息
版权信息
© 2021 The Authors; exclusive licensee Bio-protocol LLC.
如何引用
Sorokin, A., Yadav, N. S., gaudet, D. and Kovalchuk, I. (2021). Development and Standardization of Rapid and Efficient Seed Germination Protocol for Cannabis sativa. Bio-protocol 11(1): e3875. DOI: 10.21769/BioProtoc.3875.
分类
植物科学 > 植物发育生物学 > 综合
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