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Immobilization of planktonic algal spores by inkjet printing

The algal cell immobilization is a commonly used technique for treatment of waste water, production of useful metabolites and management of stock culture. However, control over the size of immobilized droplets, the population of microbes, and production rate in current techniques need to be improved...

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Autores principales: Lee, Hwa-Rim, Jung, Sang Mok, Yoon, Sejeong, Yoon, Woong Hee, Park, Tae Hee, Kim, Seongju, Shin, Hyun Woung, Hwang, Dong Soo, Jung, Sungjune
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6710280/
https://www.ncbi.nlm.nih.gov/pubmed/31451717
http://dx.doi.org/10.1038/s41598-019-48776-z
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author Lee, Hwa-Rim
Jung, Sang Mok
Yoon, Sejeong
Yoon, Woong Hee
Park, Tae Hee
Kim, Seongju
Shin, Hyun Woung
Hwang, Dong Soo
Jung, Sungjune
author_facet Lee, Hwa-Rim
Jung, Sang Mok
Yoon, Sejeong
Yoon, Woong Hee
Park, Tae Hee
Kim, Seongju
Shin, Hyun Woung
Hwang, Dong Soo
Jung, Sungjune
author_sort Lee, Hwa-Rim
collection PubMed
description The algal cell immobilization is a commonly used technique for treatment of waste water, production of useful metabolites and management of stock culture. However, control over the size of immobilized droplets, the population of microbes, and production rate in current techniques need to be improved. Here, we use drop-on-demand inkjet printing to immobilize spores of the alga Ecklonia cava within alginate microparticles for the first time. Microparticles with immobilized spores were generated by printing alginate-spore suspensions into a calcium chloride solution. We demonstrate that the inkjet technique can control the number of spores in an ejected droplet in the range of 0.23 to 1.87 by varying spore densities in bioink. After the printing-based spore encapsulation, we observe initial sprouting and continuous growth of thallus until 45 days of culture. Our study suggest that inkjet printing has a great potential to immobilize algae, and that the ability to control the number of encapsulated spores and their microenvironments can facilitate research into microscopic interactions of encapsulated spores.
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spelling pubmed-67102802019-09-13 Immobilization of planktonic algal spores by inkjet printing Lee, Hwa-Rim Jung, Sang Mok Yoon, Sejeong Yoon, Woong Hee Park, Tae Hee Kim, Seongju Shin, Hyun Woung Hwang, Dong Soo Jung, Sungjune Sci Rep Article The algal cell immobilization is a commonly used technique for treatment of waste water, production of useful metabolites and management of stock culture. However, control over the size of immobilized droplets, the population of microbes, and production rate in current techniques need to be improved. Here, we use drop-on-demand inkjet printing to immobilize spores of the alga Ecklonia cava within alginate microparticles for the first time. Microparticles with immobilized spores were generated by printing alginate-spore suspensions into a calcium chloride solution. We demonstrate that the inkjet technique can control the number of spores in an ejected droplet in the range of 0.23 to 1.87 by varying spore densities in bioink. After the printing-based spore encapsulation, we observe initial sprouting and continuous growth of thallus until 45 days of culture. Our study suggest that inkjet printing has a great potential to immobilize algae, and that the ability to control the number of encapsulated spores and their microenvironments can facilitate research into microscopic interactions of encapsulated spores. Nature Publishing Group UK 2019-08-26 /pmc/articles/PMC6710280/ /pubmed/31451717 http://dx.doi.org/10.1038/s41598-019-48776-z Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Lee, Hwa-Rim
Jung, Sang Mok
Yoon, Sejeong
Yoon, Woong Hee
Park, Tae Hee
Kim, Seongju
Shin, Hyun Woung
Hwang, Dong Soo
Jung, Sungjune
Immobilization of planktonic algal spores by inkjet printing
title Immobilization of planktonic algal spores by inkjet printing
title_full Immobilization of planktonic algal spores by inkjet printing
title_fullStr Immobilization of planktonic algal spores by inkjet printing
title_full_unstemmed Immobilization of planktonic algal spores by inkjet printing
title_short Immobilization of planktonic algal spores by inkjet printing
title_sort immobilization of planktonic algal spores by inkjet printing
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6710280/
https://www.ncbi.nlm.nih.gov/pubmed/31451717
http://dx.doi.org/10.1038/s41598-019-48776-z
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