Tropical Plant Biology

, Volume 3, Issue 2, pp 75–87

The Biotechnology Roadmap for Sugarcane Improvement

  • Carlos T. Hotta
  • Carolina G. Lembke
  • Douglas S. Domingues
  • Edgar A. Ochoa
  • Guilherme M. Q. Cruz
  • Danila M. Melotto-Passarin
  • Thiago G. Marconi
  • Melissa O. Santos
  • Marcelo Mollinari
  • Gabriel R. A. Margarido
  • Augusto César Crivellari
  • Wanderley D. dos Santos
  • Amanda P. de Souza
  • Andrea A. Hoshino
  • Helaine Carrer
  • Anete P. Souza
  • Antônio A. F. Garcia
  • Marcos S. Buckeridge
  • Marcelo Menossi
  • Marie-Anne Van Sluys
  • Glaucia M. Souza
Article

DOI: 10.1007/s12042-010-9050-5

Cite this article as:
Hotta, C.T., Lembke, C.G., Domingues, D.S. et al. Tropical Plant Biol. (2010) 3: 75. doi:10.1007/s12042-010-9050-5

Abstract

Due to the strategic importance of sugarcane to Brazil, FAPESP, the main São Paulo state research funding agency, launched in 2008 the FAPESP Bioenergy Research Program (BIOEN, http://bioenfapesp.org). BIOEN aims to generate new knowledge and human resources for the improvement of the sugarcane and ethanol industry. As part of the BIOEN program, a Workshop on Sugarcane Improvement was held on March 18th and 19th 2009 in São Paulo, Brazil. The aim of the workshop was to explore present and future challenges for sugarcane improvement and its use as a sustainable bioenergy and biomaterial feedstock. The workshop was divided in four sections that represent important challenges for sugarcane improvement: a) gene discovery and sugarcane genomics, b) transgenics and controlled transgene expression, c) sugarcane physiology (photosynthesis, sucrose metabolism, and drought) and d) breeding and statistical genetics. This report summarizes the roadmap for the improvement of sugarcane.

Keywords

Sugarcane Breeding Transgenics Genome Physiology 

Abbreviations

BIOEN

FAPESP bioenergy research program

EST

Expressed sequence tag

SUCEST

The sugarcane EST project

SAS

Sugarcane assembled sequences

BAC

Bacterial artificial chromosome

TE

Transposable element

NADP-ME

NADP+−malic enzyme

NAD-ME

NAD+−malic enzyme

PCK

Phosphoenolpyruvate carboxykinase

MAS

Marker assisted selection

SNP

Single nucleotide polymorphism

NGS

Next generation sequencing

QTL

Quantitative trait loci

Copyright information

© Springer Science+Business Media, LLC 2010

Authors and Affiliations

  • Carlos T. Hotta
    • 1
  • Carolina G. Lembke
    • 1
  • Douglas S. Domingues
    • 2
  • Edgar A. Ochoa
    • 2
  • Guilherme M. Q. Cruz
    • 2
  • Danila M. Melotto-Passarin
    • 3
  • Thiago G. Marconi
    • 4
    • 5
  • Melissa O. Santos
    • 4
    • 5
  • Marcelo Mollinari
    • 6
  • Gabriel R. A. Margarido
    • 6
  • Augusto César Crivellari
    • 2
  • Wanderley D. dos Santos
    • 2
  • Amanda P. de Souza
    • 2
  • Andrea A. Hoshino
    • 6
  • Helaine Carrer
    • 3
  • Anete P. Souza
    • 4
    • 5
  • Antônio A. F. Garcia
    • 7
  • Marcos S. Buckeridge
    • 2
  • Marcelo Menossi
    • 6
  • Marie-Anne Van Sluys
    • 2
  • Glaucia M. Souza
    • 1
  1. 1.Departamento de Bioquímica, Instituto de QuímicaUniversidade de São PauloSão PauloBrazil
  2. 2.Departamento de Botânica, Instituto de BiociênciasUniversidade de São PauloSão PauloBrazil
  3. 3.Departamento de Ciências Biológicas, Escola Superior de Agricultura Luiz de QueirozUniversidade de São PauloPiracicabaBrazil
  4. 4.Departamento de Biologia Vegetal, Instituto de BiologiaUniversidade Estadual de CampinasCampinasBrazil
  5. 5.Centro de Biologia Molecular e Engenharia GenéticaUniversidade Estadual de CampinasCampinasBrazil
  6. 6.Departamento de Genética, Evolução e Bioagentes, Instituto de BiologiaUniversidade Estadual de CampinasCampinasBrasil
  7. 7.Departamento de Genética, Escola Superior de Agricultura Luiz de QueirozUniversidade de São PauloPiracicabaBrasil

Personalised recommendations