• 1 Biotechnology and Strategic Research Division, Rubber Research Institute of Malaysia Experiment Station, 47000 Sungei Buloh, Selangor D. E., Malaysia Fax no.: +603-656-5251, , , , , , MY
  • 2 Division of Biosciences, University of Hertfordshire, Hatfield, Herts AL10 9AB, UK, , , , , , GB
  • 3 Division of Life Sciences, King's College London, Campden Hill Road, London, W8 7AH, UK, , , , , , GB
Plant Cell Rep, 1998 May;17(8):621-625.
PMID: 30736515 DOI: 10.1007/s002990050454


Hevea brasiliensis anther calli were genetically transformed using Agrobacterium GV2260 (p35SGUSINT) that harboured the β-glucuronidase (gus) and neomycin phosphotransferase (nptII) genes. β-Glucuronidase protein (GUS) was expressed in the leaves of kanamycin-resistant plants that were regnerated, and the presence of the gene was confirmed by Southern analysis. GUS was also observed to be expressed in the latex and more importantly in the serum fraction. Transverse sections of the leaf petiole from a transformed plant revealed GUS expression to be especially enhanced in the phloem and laticifers. GUS expression was subsequently detected in every one of 194 plants representing three successive vegetative cycles propagated from the original transformant. Transgenic Hevea could thus facilitate the continual production of foreign proteins expressed in the latex.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.