Protoplast isolation and transient gene expression in switchgrass, Panicum virgatum L

• Published in: Biotechnology journal 2008-03, Vol.3 (3), p.354-359
• Main Authors: Mazarei, Mitra, Al-Ahmad, Hani, Rudis, Mary R., Stewart Jr, C. Neal
• Format: Article
• Language: English
• Subjects: Cauliflower mosaic virus; Cell Separation - methods; Gene Expression Regulation, Plant - genetics; GUS; Panicum - cytology; Panicum - physiology; Panicum virgatum; PEG-mediated transformation; Plant Proteins - genetics; Plant Proteins - metabolism; Plants, Genetically Modified - metabolism; Promoter; Protein Engineering - methods; Protoplasts; Protoplasts - cytology; Protoplasts - metabolism; Switchgrass; Zea mays
• ISSN: 1860-6768; 1860-7314
• DOI: 10.1002/biot.200700189

Transient assay systems using protoplasts have been utilized in several plant species and are a powerful tool for rapid functional gene analysis and biochemical manipulations. A protoplast system has not been used in switchgrass (Panicum virgatum L.), even though it is a bioenergy crop that has received considerable attention. Here we report the first protocol to isolate large numbers of viable protoplasts from both leaves and roots of two switchgrass genotypes. Furthermore, we demonstrate transient expression of PEG‐mediated DNA uptake in the isolated protoplasts by measuring the activity of β‐glucuronidase (GUS) reporter gene driven by either the Cauliflower mosaic virus (CaMV) 35S promoter or the maize ubiquitin 1 promoter. Protoplast transformation with either the 35S or the ubiquitin promoter resulted in an increase in GUS activity compared to the untransformed controls; however, the extent of GUS activity was considerably higher for the ubiquitin promoter than for the 35S promoter. Collectively, our results indicate an efficient protoplast isolation and transient assay system that can be used to facilitate gene expression studies in switchgrass.