Establishment of Pluripotent Cell Cultures to Explore Allelopathic Activity of Coffee Cells by Protoplast Co-Culture Bioassay Method
<span style="color: windowtext;">We focused on the demonstration of a new pluripotent coffee cell culture system to control the growth and metabolic functions. Somatic cells in the epidermal layer of in vitro somatic embryos (SEs) of <i>Coffea canephora</i> expressed hig...
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doaj-fd6107738b8e4ef1bf7dcf60829eeb002020-11-25T03:11:49ZengMDPI AGPlants2223-77472020-09-0191170117010.3390/plants9091170Establishment of Pluripotent Cell Cultures to Explore Allelopathic Activity of Coffee Cells by Protoplast Co-Culture Bioassay MethodShinjiro Ogita0Muchamad Imam Asrori1Hamako Sasamoto2Department of Local Resources, Faculty of Bioresource Sciences, Prefectural University of Hiroshima, Shobara 727-0023, JapanProgram in Biological System Science, Graduate School of Comprehensive Scientific Research, Prefectural University of Hiroshima, Shobara 727-0023, JapanFaculty of Agriculture, Tokyo University of Agriculture and Technology, Fuchu 183-8509, Japan <span style="color: windowtext;">We focused on the demonstration of a new pluripotent coffee cell culture system to control the growth and metabolic functions. Somatic cells in the epidermal layer of in vitro somatic embryos (SEs) of <i>Coffea canephora</i> expressed higher pluripotency to produce secondary SEs than primary or secondary meristematic tissue. SEs were ideal explants to selectively induce functionally-differentiated cell lines, both non-embryogenic callus (nEC) and embryogenic callus (EC). The protoplast co-culture bioassay method was used to explore allelopathic activity of these cultured coffee cells. Cell wall formation of lettuce protoplasts varied after five days of co-culture. A strong stimulative reaction was observed at lower nEC protoplast densities, whereas growth was inhibited at higher densities. The reaction of lettuce protoplasts after 12 days of co-culture was recognized as an inhibitory reaction of colony formation. </span>https://www.mdpi.com/2223-7747/9/9/1170allelopathic activitycoffeedirect somatic embryogenesispluripotencyprotoplast co-culture |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Shinjiro Ogita Muchamad Imam Asrori Hamako Sasamoto |
spellingShingle |
Shinjiro Ogita Muchamad Imam Asrori Hamako Sasamoto Establishment of Pluripotent Cell Cultures to Explore Allelopathic Activity of Coffee Cells by Protoplast Co-Culture Bioassay Method Plants allelopathic activity coffee direct somatic embryogenesis pluripotency protoplast co-culture |
author_facet |
Shinjiro Ogita Muchamad Imam Asrori Hamako Sasamoto |
author_sort |
Shinjiro Ogita |
title |
Establishment of Pluripotent Cell Cultures to Explore Allelopathic Activity of Coffee Cells by Protoplast Co-Culture Bioassay Method |
title_short |
Establishment of Pluripotent Cell Cultures to Explore Allelopathic Activity of Coffee Cells by Protoplast Co-Culture Bioassay Method |
title_full |
Establishment of Pluripotent Cell Cultures to Explore Allelopathic Activity of Coffee Cells by Protoplast Co-Culture Bioassay Method |
title_fullStr |
Establishment of Pluripotent Cell Cultures to Explore Allelopathic Activity of Coffee Cells by Protoplast Co-Culture Bioassay Method |
title_full_unstemmed |
Establishment of Pluripotent Cell Cultures to Explore Allelopathic Activity of Coffee Cells by Protoplast Co-Culture Bioassay Method |
title_sort |
establishment of pluripotent cell cultures to explore allelopathic activity of coffee cells by protoplast co-culture bioassay method |
publisher |
MDPI AG |
series |
Plants |
issn |
2223-7747 |
publishDate |
2020-09-01 |
description |
<span style="color: windowtext;">We focused on the demonstration of a new pluripotent coffee cell culture system to control the growth and metabolic functions. Somatic cells in the epidermal layer of in vitro somatic embryos (SEs) of <i>Coffea canephora</i> expressed higher pluripotency to produce secondary SEs than primary or secondary meristematic tissue. SEs were ideal explants to selectively induce functionally-differentiated cell lines, both non-embryogenic callus (nEC) and embryogenic callus (EC). The protoplast co-culture bioassay method was used to explore allelopathic activity of these cultured coffee cells. Cell wall formation of lettuce protoplasts varied after five days of co-culture. A strong stimulative reaction was observed at lower nEC protoplast densities, whereas growth was inhibited at higher densities. The reaction of lettuce protoplasts after 12 days of co-culture was recognized as an inhibitory reaction of colony formation. </span> |
topic |
allelopathic activity coffee direct somatic embryogenesis pluripotency protoplast co-culture |
url |
https://www.mdpi.com/2223-7747/9/9/1170 |
work_keys_str_mv |
AT shinjiroogita establishmentofpluripotentcellculturestoexploreallelopathicactivityofcoffeecellsbyprotoplastcoculturebioassaymethod AT muchamadimamasrori establishmentofpluripotentcellculturestoexploreallelopathicactivityofcoffeecellsbyprotoplastcoculturebioassaymethod AT hamakosasamoto establishmentofpluripotentcellculturestoexploreallelopathicactivityofcoffeecellsbyprotoplastcoculturebioassaymethod |
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1724652802383282176 |