{"title":"Enhanced rooting and shoot proliferation in micropropagation of ‘MKR1’ dwarfing persimmon rootstock","authors":"Ziaurrahman Hejazi , Chitose Honsho , Takuya Tetsumura","doi":"10.1016/j.bcab.2024.103487","DOIUrl":null,"url":null,"abstract":"<div><div>Persimmon rootstocks (<em>Diospyros kaki</em> Thunb.) are typically propagated from seedling rootstocks, but this often results in excessive vigor and inconsistent growth, complicating orchard management. This study aimed to improve a micropropagation protocol for ‘MKR1,’ a dwarfing persimmon rootstock, based on the method of Tao and Sugiura (1992). Both zeatin, an expensive cytokinin, and BA, a more affordable option, were evaluated for <em>in vitro</em> shoot tip establishment and proliferation. Microcuttings grown on full-strength MS medium showed higher rooting and survival rates than those on MS (1/2 N), commonly used for persimmons. After 60 subcultures, BA-treated shoots experienced reduced proliferation rates, which were restored with a low concentration of zeatin without affecting rooting. The original protocol, which required 40 days of culturing in agar-solidified medium followed by transplanting to vermiculite-filled pots, proved cumbersome. A direct rooting method, involving immediate potting after quick-dip IBA treatment, was unsuccessful. However, a semi-direct method with a 10-day dark incubation prior to transplanting produced comparable rooting rates to the original method. Further, adding IBA directly to the medium eliminated the need for quick-dip treatments, allowing successful transplanting into peat pellets after 10 days, achieving high rooting success and robust plantlet growth. This streamlined protocol reduces production time and costs, offering an efficient approach for large-scale propagation of ‘MKR1’ plantlets.</div></div>","PeriodicalId":8774,"journal":{"name":"Biocatalysis and agricultural biotechnology","volume":"64 ","pages":"Article 103487"},"PeriodicalIF":3.8000,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biocatalysis and agricultural biotechnology","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1878818124004717","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/12/30 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"BIOTECHNOLOGY & APPLIED MICROBIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Persimmon rootstocks (Diospyros kaki Thunb.) are typically propagated from seedling rootstocks, but this often results in excessive vigor and inconsistent growth, complicating orchard management. This study aimed to improve a micropropagation protocol for ‘MKR1,’ a dwarfing persimmon rootstock, based on the method of Tao and Sugiura (1992). Both zeatin, an expensive cytokinin, and BA, a more affordable option, were evaluated for in vitro shoot tip establishment and proliferation. Microcuttings grown on full-strength MS medium showed higher rooting and survival rates than those on MS (1/2 N), commonly used for persimmons. After 60 subcultures, BA-treated shoots experienced reduced proliferation rates, which were restored with a low concentration of zeatin without affecting rooting. The original protocol, which required 40 days of culturing in agar-solidified medium followed by transplanting to vermiculite-filled pots, proved cumbersome. A direct rooting method, involving immediate potting after quick-dip IBA treatment, was unsuccessful. However, a semi-direct method with a 10-day dark incubation prior to transplanting produced comparable rooting rates to the original method. Further, adding IBA directly to the medium eliminated the need for quick-dip treatments, allowing successful transplanting into peat pellets after 10 days, achieving high rooting success and robust plantlet growth. This streamlined protocol reduces production time and costs, offering an efficient approach for large-scale propagation of ‘MKR1’ plantlets.
柿子砧木(Diospyros kaki Thunb.)通常由幼苗砧木繁殖,但这通常导致过度活力和不稳定的生长,使果园管理复杂化。本研究旨在基于Tao和Sugiura(1992)的方法,改进矮化柿子砧木“MKR1”的微繁方案。玉米素(一种昂贵的细胞分裂素)和BA(一种更便宜的选择)对离体茎尖的建立和增殖进行了评估。在全强度MS培养基上培养的扦插生根率和成活率均高于常备柿子的MS (1/2 N)培养基。经过60次传代培养后,ba处理的芽的增殖率降低,在低浓度玉米素的处理下,芽的增殖率恢复,但不影响生根。最初的方案需要在琼脂固化培养基中培养40天,然后移植到充满蛭石的花盆中,这被证明是繁琐的。直接生根方法,即在快速浸渍IBA处理后立即盆栽,不成功。然而,在移栽前进行10天黑暗培养的半直接方法的生根率与原始方法相当。此外,将IBA直接添加到培养基中,无需快速浸渍处理,可以在10天后成功移植到泥炭颗粒中,实现高生根成功率和强劲的植株生长。这种简化的方案减少了生产时间和成本,为“MKR1”植株的大规模繁殖提供了有效的方法。
期刊介绍:
Biocatalysis and Agricultural Biotechnology is the official journal of the International Society of Biocatalysis and Agricultural Biotechnology (ISBAB). The journal publishes high quality articles especially in the science and technology of biocatalysis, bioprocesses, agricultural biotechnology, biomedical biotechnology, and, if appropriate, from other related areas of biotechnology. The journal will publish peer-reviewed basic and applied research papers, authoritative reviews, and feature articles. The scope of the journal encompasses the research, industrial, and commercial aspects of biotechnology, including the areas of: biocatalysis; bioprocesses; food and agriculture; genetic engineering; molecular biology; healthcare and pharmaceuticals; biofuels; genomics; nanotechnology; environment and biodiversity; and bioremediation.