IN VITRO PLANT REGENERATION IN LOCAL AUS RICE THROUGH MATURED SEED CULTURE

نویسندگان

چکیده

An investigation was carried out to decipher the effect of genotypes and concentrations growth regulators for callus induction subsequent plant regeneration from mature seeds rice. Two local rice cultivars viz. Nayanmony Kalomona two 2, 4-D NAA were used evaluate their performance. The cultured under aseptic condition onto MS basal medium at varying combinations (1.0, 1.5 2.0 mgL- 1) (0.0, 0.5 1.0 mgL-1) induction. For fortified with 1 3.0 mgL-1 BAP applied. Between showed better responses in frequency (91.38%), weight (0.90 g)as well as diameter (7.48 mm). Among (1.5 alone produced best (95.16%) highest (1.88 g) but (8.27 mm) +0.5 NAA. It observed that both genotype regulator significantly affected regeneration. supplemented + NAA0.0 exhibited performance (99.33%) (1.92 cultivar whereas (8.38 NAA0.5 mgL-1. performed regarding (88.15%) compared (86.67%). Plantlets derived mgL-1+ 0.0 results survival. Therefore, it is suggested application 2,4-D advantageous accomplish overall efficiency induction, survival cultivars. Thus, selection responsive like would be beneficial transformation attempts improve crop.

برای دانلود باید عضویت طلایی داشته باشید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

In vitro shoot Proliferation of Hypericum perforatum L. through Indirect and Direct Plant Regeneration

Hypericum perforatum L. (St. Johns’ wort) is the most commercially important species of the genus Hypericum and contains a wide range of components including naphthodianthrones, phloroglucinols, tannins, xanthones, phenolic acids and essential oil. In order to establish an efficient protocol for regeneration, the effects of explant type and plant growth regulators on direct and indirect shoot r...

متن کامل

Regeneration of Stevia Plant Through Callus Culture

Stevia rebaudiana Bertoni that conventionally propagated by seed or by cuttings or clump division which has a limitation of quality and quantity seed material. In present study, callus culture technique was tried to achieve rapid plant multiplication for quality seed material. Callus induction and multiplication medium was standardized from nodal as well as leaf sagments. It is possible to main...

متن کامل

The Improvement of Cow Tail (Smirnovia iranica) Seed Germination through in vitro Culture

Extended Abstract Introduction: Cow tail (Smirnovia iranica) is considered a valuable shrub species indigenous and adapted to the sandy lands of the Iranian central regions which besides playing an essential role in the desert cover for soil protection and of forage production, is considered important due to its great medicinal values. Considering the fact that seed germination of this plant d...

متن کامل

In Vitro Flower Bud Formation, Plant Regeneration and Morphogenetic Studies in Local Scented Cultivar of Rosa indica

In vitro propagation of rose (Rosa indica) as well as rose breeding is a valuable economic enterprise and has received highest importance globally including Indian subcontinent. The development of new cultivars for commerce is faced with new challenges. In vitro micropropagation protocols of varieties of roses have been established but very few reports on the clonal propagation of local cultiva...

متن کامل

Efficient in Vitro Plant Regeneration

An efficient plant regeneration system for Pinellia ternata (Thunb) Breit, an important wild Chinese herb, was established. The investigated factors influencing callus induction and plant regeneration included sterilizing agents, explant type, culture medium, and combinations of plant growth regulators in the medium. Ten min treatment of explants with 0.1% HgCl2 was more suitable for sterilizat...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

ژورنال

عنوان ژورنال: Khulna University studies

سال: 2022

ISSN: ['1563-0897', '2789-2697']

DOI: https://doi.org/10.53808/kus.2017.14.1and2.1617-l