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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Main Authors: Shinjiro Ogita, Muchamad Imam Asrori, Hamako Sasamoto
Format: Article
Language:English
Published: MDPI AG 2020-09-01
Series:Plants
Subjects:
Online Access:https://www.mdpi.com/2223-7747/9/9/1170
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spelling 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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