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What are Carbohydrates?

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Sugar (a simple carbohydrate) metabolism (chemical reactions) is a classic example of the many cellular processes that use and produce energy. Living things consume sugar as a major energy source because sugar molecules have considerable energy stored within their bonds. Consumed carbohydrates have their origins in photosynthesizing organisms like plants. During photosynthesis, plants use the energy of sunlight to convert carbon dioxide gas into sugar molecules, like glucose. Because this...
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Updated: Jul 19, 2026

Multipronged Phenotyping Approaches to Characterize Sugarcane Root Systems
09:21

Multipronged Phenotyping Approaches to Characterize Sugarcane Root Systems

Published on: August 17, 2022

Sugarcane (Saccharum spp.).

Ariel D Arencibia1, Elva R Carmona

  • 1Genetic and Phytopathologic Department, National Institute for Sugarcane Research, Carretera CUJAE Km 2. Boyeros 19 390, Havana City, Cuba.

Methods in Molecular Biology (Clifton, N.J.)
|October 13, 2006
PubMed
Summary

This study details methods for creating transgenic sugarcane using Agrobacterium tumefaciens. Optimized tissue culture and specific Agrobacterium strains are key for successful genetic engineering of sugarcane.

Area of Science:

  • Plant Biotechnology
  • Agricultural Science
  • Molecular Biology

Background:

  • Sugarcane (Saccharum spp.) genetic improvement is essential for agricultural productivity.
  • Efficient transformation protocols are needed for advanced breeding and genetic engineering of sugarcane.
  • Agrobacterium tumefaciens-mediated transformation is a primary method for plant genetic engineering.

Purpose of the Study:

  • To describe reliable procedures for generating transgenic sugarcane.
  • To highlight critical factors for successful Agrobacterium-mediated sugarcane transformation.
  • To present adaptable protocols for various sugarcane genotypes.

Main Methods:

  • Co-cultivation of sugarcane calli and in vitro plants with Agrobacterium tumefaciens.

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  • Utilizing super-binary vectors or super-virulent Agrobacterium strains.
  • Implementing optimized plant regeneration via calli culture and micropropagation strategies.
  • Main Results:

    • Successful recovery of transgenic sugarcane through described co-cultivation procedures.
    • Demonstration that specific tissue culture strategies and Agrobacterium strains are crucial.
    • Optimization of regeneration and micropropagation for a broad range of sugarcane genotypes.
    • Identification of four selective micropropagation steps to eliminate chimera plants in in vitro plant transformation.

    Conclusions:

    • The presented procedures are adaptable for the genetic engineering of diverse Saccharum spp. genotypes.
    • Optimized tissue culture and Agrobacterium strains are vital for efficient sugarcane transformation.
    • The protocol provides a foundation for advancing sugarcane genetic improvement and research.