Overexpression of polyphenol oxidase in transgenic sugarcane results in darker juice and raw sugar

Color intensity of raw sugar is, in part, a result of the activity of the enzyme polyphenol oxidase (PPO) acting on phenolic compounds to produce dark colored polymers when sugarcane (Saccharum spp.) is crushed to release the juice. Paler colored sugar has a potential market premium over darker sugar. In an attempt to alter the level of PPO activity in transgenic plants, sense and antisense constructs containing the native sugarcane PPO gene were introduced into sugarcane by biolistics. In a series of field experiments, it was demonstrated that PPO activity among clones correlated significantly with juice color. In laboratory crystallizations of raw sugar using juice derived from clones with high and low PPO activity, the juice with the higher PPO activity produced darker colored crystals. PPO activity was elevated and juice color was darker in all types of transgenic plants. However, clones derived from a sense construct had higher PPO activity than the other transgenic clones, tissue culture control clones, or cultivars. Furthermore, northern blot analysis demonstrated that PPO sense transgenics had much higher levels of PPO transcripts in the stem than other clones. This is the first targeted manipulation of an endogenous metabolic enzyme-encoding gene in sugarcane that leads to altered enzyme activity. Although low PPO lines with good agronomic performance were not generated, this research demonstrates the principle that juice and sugar color are correlated with PPO activity, consistent with the hypothesis that lowering PPO activity in sugarcane could reduce the color intensity of juice and raw sugar.

[1]  Alfred M. Mayer,et al.  Polyphenol oxidases in plants , 1979 .

[2]  I. Dry,et al.  Isolation of a full-length cDNA encoding polyphenol oxidase from sugarcane, a C4 grass , 1996, Plant Molecular Biology.

[3]  S. D. Purohit,et al.  BIOCHEMICAL CHARACTERISTICS OF DIFFERENTIATING CALLUS CULTURES OF FERONIA LIMONIA L. , 1996 .

[4]  D. Corsini,et al.  Control of enzymatic browning in potato (Solanum tuberosum L.) by sense and antisense RNA from tomato polyphenol oxidase. , 2001, Journal of agricultural and food chemistry.

[5]  H. Goodman,et al.  Nopaline synthase: transcript mapping and DNA sequence. , 1982, Journal of molecular and applied genetics.

[6]  P. Waterhouse,et al.  Construct design for efficient, effective and high-throughput gene silencing in plants. , 2001, The Plant journal : for cell and molecular biology.

[7]  S. Duke,et al.  Polyphenol oxidase: The chloroplast oxidase with no established function , 1988 .

[8]  C. Bachem,et al.  Antisense Expression of Polyphenol Oxidase Genes Inhibits Enzymatic Browning in Potato Tubers , 1994, Bio/Technology.

[9]  R. Birch,et al.  High-efficiency, microprojectile-mediated cotransformation of sugarcane, using visible or selectable markers , 2004, Molecular Breeding.

[10]  W. Peacock,et al.  pEmu: an improved promoter for gene expression in cereal cells , 1991, Theoretical and Applied Genetics.

[11]  C. Napoli,et al.  Introduction of a Chimeric Chalcone Synthase Gene into Petunia Results in Reversible Co-Suppression of Homologous Genes in trans. , 1990, The Plant cell.

[12]  H. Vaucheret,et al.  Molecular and genetic analysis of nitrite reductase co-suppression in transgenic tobacco plants , 1995, Molecular and General Genetics MGG.

[13]  P. Quail,et al.  Maize polyubiquitin genes: structure, thermal perturbation of expression and transcript splicing, and promoter activity following transfer to protoplasts by electroporation , 1992, Plant Molecular Biology.

[14]  Li Li,et al.  Overexpression of polyphenol oxidase in transgenic tomato plants results in enhanced bacterial disease resistance , 2002, Planta.

[15]  S. Robinson,et al.  Contribution of enzymic browning to color in sugarcane juice , 1994 .

[16]  I. Dry,et al.  Molecular cloning and characterisation of grape berry polyphenol oxidase , 1994, Plant Molecular Biology.