Protein Profile of Tissue Culture of TRI2025 Tea Clone
Tea is well known as favourite healthy drink for almost all people over the world. Tea propagation using conventional and modern ways are now developing rapidly. However, information regarding the protein profile of tissue culture of tea plant has not been revealed yet. This study aimed to determine...
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Universitas Negeri Semarang
2019-04-01
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doaj-384d3eb59482453688e4531b6859f09d2020-11-25T02:10:41ZengUniversitas Negeri SemarangBiosaintifika: Journal of Biology & Biology Education2085-191X2338-76102019-04-0111181410.15294/biosaintifika.v11i1.175228453Protein Profile of Tissue Culture of TRI2025 Tea CloneRatna Dewi Eskundari0Taryono Taryono1Didik Indradewa2Yekti Asih Purwestri3Department of Biotechnology, Graduate School, Gadjah Mada University, IndonesiaFaculty of Agriculture, Gadjah Mada University, IndonesiaFaculty of Agriculture, Gadjah Mada University, IndonesiaFaculty of Biology, Gadjah Mada University, IndonesiaTea is well known as favourite healthy drink for almost all people over the world. Tea propagation using conventional and modern ways are now developing rapidly. However, information regarding the protein profile of tissue culture of tea plant has not been revealed yet. This study aimed to determine the difference of protein profile of tea’s tissue culture using SDS-PAGE. This study was conducted using embryonic axes of TRI2025 tea clone cultured on MS media supplemented with 2,4-D for inducing somatic embryogenesis and globular-like structure (GLS) regeneration, and MS media supplemented with BAP for inducing shoot via organogenesis. The results revealed that proteins in the size of 37.69; 54.89; 60.77; 71.35; 87.34; and 92.99 KDa might be involved at somatic embryogenesis, and about 38.69 KDa, 69.27 KDa, and 55.76 KDa respectively for GLS, initiation of shoot, and initiation of GLS derived leaf. Predicted key protein for leaf initiation both directly or through GLS was about 31-33 KDa, while for callusing were about 27.56 and 52.73 KDa, and constitutive protein was about 22.75 KDa. This study provides the first report of protein profile of tea’s tissue culture. The information obtained can be beneficial as a marker for explant for somatic embryogenesis, GLS, or organogenesis pathway and as a scientific information for further biotechnology development.https://journal.unnes.ac.id/nju/index.php/biosaintifika/article/view/17522camellia sinensis l.proteinteatissue culture |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Ratna Dewi Eskundari Taryono Taryono Didik Indradewa Yekti Asih Purwestri |
spellingShingle |
Ratna Dewi Eskundari Taryono Taryono Didik Indradewa Yekti Asih Purwestri Protein Profile of Tissue Culture of TRI2025 Tea Clone Biosaintifika: Journal of Biology & Biology Education camellia sinensis l. protein tea tissue culture |
author_facet |
Ratna Dewi Eskundari Taryono Taryono Didik Indradewa Yekti Asih Purwestri |
author_sort |
Ratna Dewi Eskundari |
title |
Protein Profile of Tissue Culture of TRI2025 Tea Clone |
title_short |
Protein Profile of Tissue Culture of TRI2025 Tea Clone |
title_full |
Protein Profile of Tissue Culture of TRI2025 Tea Clone |
title_fullStr |
Protein Profile of Tissue Culture of TRI2025 Tea Clone |
title_full_unstemmed |
Protein Profile of Tissue Culture of TRI2025 Tea Clone |
title_sort |
protein profile of tissue culture of tri2025 tea clone |
publisher |
Universitas Negeri Semarang |
series |
Biosaintifika: Journal of Biology & Biology Education |
issn |
2085-191X 2338-7610 |
publishDate |
2019-04-01 |
description |
Tea is well known as favourite healthy drink for almost all people over the world. Tea propagation using conventional and modern ways are now developing rapidly. However, information regarding the protein profile of tissue culture of tea plant has not been revealed yet. This study aimed to determine the difference of protein profile of tea’s tissue culture using SDS-PAGE. This study was conducted using embryonic axes of TRI2025 tea clone cultured on MS media supplemented with 2,4-D for inducing somatic embryogenesis and globular-like structure (GLS) regeneration, and MS media supplemented with BAP for inducing shoot via organogenesis. The results revealed that proteins in the size of 37.69; 54.89; 60.77; 71.35; 87.34; and 92.99 KDa might be involved at somatic embryogenesis, and about 38.69 KDa, 69.27 KDa, and 55.76 KDa respectively for GLS, initiation of shoot, and initiation of GLS derived leaf. Predicted key protein for leaf initiation both directly or through GLS was about 31-33 KDa, while for callusing were about 27.56 and 52.73 KDa, and constitutive protein was about 22.75 KDa. This study provides the first report of protein profile of tea’s tissue culture. The information obtained can be beneficial as a marker for explant for somatic embryogenesis, GLS, or organogenesis pathway and as a scientific information for further biotechnology development. |
topic |
camellia sinensis l. protein tea tissue culture |
url |
https://journal.unnes.ac.id/nju/index.php/biosaintifika/article/view/17522 |
work_keys_str_mv |
AT ratnadewieskundari proteinprofileoftissuecultureoftri2025teaclone AT taryonotaryono proteinprofileoftissuecultureoftri2025teaclone AT didikindradewa proteinprofileoftissuecultureoftri2025teaclone AT yektiasihpurwestri proteinprofileoftissuecultureoftri2025teaclone |
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