Starting Strong: Optimizing Micropropagation Protocols for Sugarcane US-718 | InformativeBD

Initiation protocol optimization of (Saccharum officinarum L.) variety US- 718 through micropropagtion techniques

Naseem Khatoon Bhurgri, from the institute of Pakistan. wrote a Research article about, Starting Strong: Optimizing Micropropagation Protocols for Sugarcane US-718. Entitled, Initiation protocol optimization of (Saccharum officinarum L.) variety US- 718 through micropropagtion techniques. This research paper published by the Journal of Biodiversity and Environmental Sciences | JBES.  an open access scholarly research journal on Biodiversity. under the affiliation of the International Network For Natural Sciences| INNSpub. an open access multidisciplinary research journal publisher.

Abstract

The sugarcane varietyUS-718 experimentally was carried out in changed concentration of BAP and kinetin under established condition of invitro along with replications in complete randomized design. The purpose of the study was to determine the optimum concentration in presence of combination of BAP and kinetin under invitro condition .In MS neutering media the variety US-718 shown maximum result of 90.32% shoot initiation in 3.5#0.5 of shoots per explant in concentrations of 1.5mg/l BAP without kinetin exhibited a better response than other concentration.

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Introduction

Sugarcane belong to Poaceae family is a strong and major crop of Pakistan. It consists high sugar content. (Saccharum officinarum) contributes 60-70% of annual sugar production in the world (Shakra Jamil 2017). Sugarcane is a perennial grass family crops that reproduction through sexual and asexual modes. It reproduces asexually by three or two buds stem cutting called sets, and advanced methodologies of in vitro propagation by taking parts of it such as shoot tip, apical merited, axillary bud and leaf. It also reproduces through seed propagation via flower (Fuzz), which is used for breeding purposes (Sime M2013). The sugarcane is used in production of paper, antibiotics, dextran, waxes and fats, epoxy polymers and bio fertilizers as reported by DSD, 2013. FAO 2014 .The sugarcane is economically vital industrial crop and well propagated conservatively by sets, but enormous land requirement, potential transfers of pathogens through seed and conventional method from generation to generation are the main factors for low rate propagation The invitro propagation is a greatest substitute to overcome such factors and pave the way to produce disease free and enough amount of planting material. (Belet Getnet 2017).

Clonal propagation through tissue culture is the one of the extensively accepted methods used for the commercial production of genetically enhanced quality of crops (Tiwari et al., 2012). During tissue culture, pathogenic and non-pathogenic fungi and bacteria are exposed as contaminants and therefore can regularly be disposed of. Systemic viruses which are much more difficult to eliminate the sugarcane intensive persistent contamination has been frequently reported in many tissue culture system, despite, the use of strong surface sterilization treatments of explants (Anonymous. 2009). Micropropagtion is however actual subtle methods which needs sterile condition in each stage (0-4) specifically for establishment of surface sterilization of explants initiation and establishment of aseptic culture, multiplication, rooting and acclimatization. These steps manifested the sensitivity of tissue cultures techniques in determination of contamination and economic significance rather than conventional propagation. These techniques facilitates to grower to permit the sugar industry estates to produce adequate planting material with short time period and cost effective (Lakshman p. et al., 2006).

Shoot tip initiation observed at different concentration by BAP and Kin in many plant culture systems (G. Zahra et al., 2010). The success of the sugarcane tissue culture is also dependent of sugarcane varieties. (C. Ganonou et al., 2005), the tissue culturing medium and use of growth enhancer and regulators (V. Saharan et al 2004). Therefor the present study on sugarcane variety US-718 was carried out by plant tissue culture laboratory Khoski Sugar mill Badin, to detect the influence of dissimilar media compositions on the initiation of sugarcane variety US-718. We have also carried out optimization of initiation protocol for in vitro propagation of sugarcane variety US-718.

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