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High-Level Production of Recombinant Snowdrop Lectin in Sugarcane and Energy Cane.
Padilla, Carmen S; Damaj, Mona B; Yang, Zhong-Nan; Molina, Joe; Berquist, Brian R; White, Earl L; Solís-Gracia, Nora; Da Silva, Jorge; Mandadi, Kranthi K.
Afiliação
  • Padilla CS; Texas A&M AgriLife Research and Extension Center, Weslaco, TX, United States.
  • Damaj MB; Texas A&M AgriLife Research and Extension Center, Weslaco, TX, United States.
  • Yang ZN; Institute for Plant Gene Function, Department of Biology, Shanghai Normal University, Shanghai, China.
  • Molina J; Texas A&M AgriLife Research and Extension Center, Weslaco, TX, United States.
  • Berquist BR; iBio, Bryan, TX, United States.
  • White EL; MDx BioAnalytical Laboratory, Inc., College Station, TX, United States.
  • Solís-Gracia N; Texas A&M AgriLife Research and Extension Center, Weslaco, TX, United States.
  • Da Silva J; Texas A&M AgriLife Research and Extension Center, Weslaco, TX, United States.
  • Mandadi KK; Department of Soil and Crop Sciences, Texas A&M University, College Station, TX, United States.
Article em En | MEDLINE | ID: mdl-33015000
ABSTRACT
Sugarcane and energy cane (Saccharum spp. hybrids) are ideal for plant-based production of recombinant proteins because their high resource-use efficiency, rapid growth and efficient photosynthesis enable extensive biomass production and protein accumulation at a cost-effective scale. Here, we aimed to develop these species as efficient platforms to produce recombinant Galanthus nivalis L. (snowdrop) agglutinin (GNA), a monocot-bulb mannose-specific lectin with potent antiviral, antifungal and antitumor activities. Initially, GNA levels of 0.04% and 0.3% total soluble protein (TSP) (0.3 and 3.8 mg kg-1 tissue) were recovered from the culms and leaves, respectively, of sugarcane lines expressing recombinant GNA under the control of the constitutive maize ubiquitin 1 (Ubi) promoter. Co-expression of recombinant GNA from stacked multiple promoters (pUbi and culm-regulated promoters from sugarcane dirigent5-1 and Sugarcane bacilliform virus) on separate expression vectors increased GNA yields up to 42.3-fold (1.8% TSP or 12.7 mg kg-1 tissue) and 7.7-fold (2.3% TSP or 29.3 mg kg-1 tissue) in sugarcane and energy cane lines, respectively. Moreover, inducing promoter activity in the leaves of GNA transgenic lines with stress-regulated hormones increased GNA accumulation to 2.7% TSP (37.2 mg kg-1 tissue). Purification by mannose-agarose affinity chromatography yielded a functional sugarcane recombinant GNA with binding substrate specificity similar to that of native snowdrop-bulb GNA, as shown by enzyme-linked lectin and mannose-binding inhibition assays. The size and molecular weight of recombinant GNA were identical to those of native GNA, as determined by size-exclusion chromatography and MALDI-TOF mass spectrometry. This work demonstrates the feasibility of producing recombinant GNA at high levels in Saccharum species, with the long-term goal of using it as a broad-spectrum antiviral carrier molecule for hemopurifiers and in related therapeutic applications.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Front Bioeng Biotechnol Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Front Bioeng Biotechnol Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Estados Unidos