Soft material-based microculture system having air permeable cover sheet for the protoplast culture of Nicotiana tabacum

• Published in: Bioprocess and biosystems engineering Vol. 29; no. 3; pp. 163 - 168
• Main Authors: JONG II JU, KO, Jung-Moon, SO HYEON KIM, JU YEOUL BAEK, CHA, Hyeon-Cheol, SANG HOON LEE
• Format: Journal Article
• Language: English
• Published: Berlin Springer 01.08.2006; Springer Nature B.V
• Subjects: Air; Biological and medical sciences; Biotechnology; Cell culture; Cell Culture Techniques - instrumentation; Cell Culture Techniques - methods; Cells, Cultured; Dimethylpolysiloxanes - chemistry; Elasticity; Equipment Design; Equipment Failure Analysis; Experimental methods; Fundamental and applied biological sciences. Psychology; Materials Testing; Membranes, Artificial; Microfluidics - instrumentation; Microfluidics - methods; Nicotiana - cytology; Nicotiana - growth & development; Permeability; Protoplasts - cytology; Protoplasts - physiology; Silicones - chemistry; Ultrafiltration - instrumentation; Ultrafiltration - methods; Cell culture; Air permeability; Dicotyledones; Protoplast; Angiospermae; Polydimethylsiloxane (PDMS); Spermatophyta; Solanaceae; Air; Permeability; CPW; Nicotiana tabacum
• ISSN: 1615-7591; 1615-7605
• DOI: 10.1007/s00449-006-0068-x

In plant cell culture, the delivery of nutrition and gas (mainly oxygen) to the cells is the most important factor for viability. In this paper, we propose a polydimethylsiloxane (PDMS)-based microculture system that is designed to have good aeration. PDMS is known to have excellent air permeability, and through the experimental method, we investigated the relation between the degree of air delivery and the thickness of the PDMS sheet covering the culture chamber. We determined the proper thickness of the cover sheet, and cultured protoplasts of Nicotiana tabacum in a culture chamber covered with a PDMS sheet having thickness of 400 microm. The cells were successfully divided, and lived well inside the culture chamber for 10 days. In addition, protoplasts were cultured inside the culture chambers covered with the cover glass and the PDMS sheet, respectively, and the microcolonies were formed well inside the PDMS covered chamber after 10 days.