Expression levels of the three candidate genes of PEP4 .

The expression frequency of the three orthologous gene was analyzed based on the read number obtained by sequence analysis of mRNA using MiSeq. Total RNA was isolated from cells using ISOGEN (Wako) according to the manufacturer’s instructions as follows. Cells were ground in liquid nitrogen to a fin...

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Main Authors: Natsuki Omae (10318504), Yuka Sameshima-Yamashita (6292238), Kazunori Ushimaru (3689119), Hideaki Koike (410323), Hiroko Kitamoto (6076307), Tomotake Morita (526538)
Format: Still Image
Language:unknown
Published: 2021
Subjects:
GB
PaE
Online Access:https://doi.org/10.1371/journal.pone.0247462.s007
id ftsmithonian:oai:figshare.com:article/14230969
record_format openpolar
spelling ftsmithonian:oai:figshare.com:article/14230969 2023-05-15T13:43:17+02:00 Expression levels of the three candidate genes of PEP4 . Natsuki Omae (10318504) Yuka Sameshima-Yamashita (6292238) Kazunori Ushimaru (3689119) Hideaki Koike (410323) Hiroko Kitamoto (6076307) Tomotake Morita (526538) 2021-03-17T17:38:25Z https://doi.org/10.1371/journal.pone.0247462.s007 unknown https://figshare.com/articles/figure/Expression_levels_of_the_three_candidate_genes_of_i_PEP4_i_/14230969 doi:10.1371/journal.pone.0247462.s007 CC BY 4.0 CC-BY Biophysics Biochemistry Microbiology Cell Biology Genetics Molecular Biology Developmental Biology Science Policy Infectious Diseases Biological Sciences not elsewhere classified Chemical Sciences not elsewhere classified vacuolar protease function yeast Pseudozyma antarctica GB plastic-degrading enzyme 48 h incubation orthologous genes encoding proteases 3- L jar fermenter XG 8 XG 8 Δ Pa strain XG 8 control B orthologous genes PaE degradation fragments Δ Pa Image Figure 2021 ftsmithonian https://doi.org/10.1371/journal.pone.0247462.s007 2021-03-23T16:29:07Z The expression frequency of the three orthologous gene was analyzed based on the read number obtained by sequence analysis of mRNA using MiSeq. Total RNA was isolated from cells using ISOGEN (Wako) according to the manufacturer’s instructions as follows. Cells were ground in liquid nitrogen to a fine powder, and approximately 3 g was mixed with 15 ml ISOGEN solution, followed by the addition of 3 ml chloroform. The mixture was left at room temperature for 3 min and centrifuged at 2,300 g for 20 min. The supernatant was transferred to a fresh tube and mixed with 7.5 ml isopropanol. The mixture was left at room temperature for 10 min and centrifuged at 2,300 g for 20 min. The pellet was dried and dissolved in 300 μl of RNase-free water. mRNA was purified from approximately 200 μg total RNA using an OligotexTM-dT30 mRNA Purification kit (Takara, Shiga, Japan) according to the manufacturer’s instructions. The library was prepared with TruSeq Stranded mRNA Library Prep (Illumina Inc., San Diego, CA, USA), and obtained the sequences with MiSeq (Illumina) according to the manufacturer’s instructions. Read number of each nucleotid was viewed with IGV [ 30 ]. (TIF) Still Image Antarc* Antarctica Unknown
institution Open Polar
collection Unknown
op_collection_id ftsmithonian
language unknown
topic Biophysics
Biochemistry
Microbiology
Cell Biology
Genetics
Molecular Biology
Developmental Biology
Science Policy
Infectious Diseases
Biological Sciences not elsewhere classified
Chemical Sciences not elsewhere classified
vacuolar protease function
yeast Pseudozyma antarctica
GB
plastic-degrading enzyme
48 h incubation
orthologous genes encoding proteases
3- L jar fermenter
XG 8
XG 8 Δ Pa
strain
XG 8 control
B orthologous genes
PaE
degradation fragments
Δ Pa
spellingShingle Biophysics
Biochemistry
Microbiology
Cell Biology
Genetics
Molecular Biology
Developmental Biology
Science Policy
Infectious Diseases
Biological Sciences not elsewhere classified
Chemical Sciences not elsewhere classified
vacuolar protease function
yeast Pseudozyma antarctica
GB
plastic-degrading enzyme
48 h incubation
orthologous genes encoding proteases
3- L jar fermenter
XG 8
XG 8 Δ Pa
strain
XG 8 control
B orthologous genes
PaE
degradation fragments
Δ Pa
Natsuki Omae (10318504)
Yuka Sameshima-Yamashita (6292238)
Kazunori Ushimaru (3689119)
Hideaki Koike (410323)
Hiroko Kitamoto (6076307)
Tomotake Morita (526538)
Expression levels of the three candidate genes of PEP4 .
topic_facet Biophysics
Biochemistry
Microbiology
Cell Biology
Genetics
Molecular Biology
Developmental Biology
Science Policy
Infectious Diseases
Biological Sciences not elsewhere classified
Chemical Sciences not elsewhere classified
vacuolar protease function
yeast Pseudozyma antarctica
GB
plastic-degrading enzyme
48 h incubation
orthologous genes encoding proteases
3- L jar fermenter
XG 8
XG 8 Δ Pa
strain
XG 8 control
B orthologous genes
PaE
degradation fragments
Δ Pa
description The expression frequency of the three orthologous gene was analyzed based on the read number obtained by sequence analysis of mRNA using MiSeq. Total RNA was isolated from cells using ISOGEN (Wako) according to the manufacturer’s instructions as follows. Cells were ground in liquid nitrogen to a fine powder, and approximately 3 g was mixed with 15 ml ISOGEN solution, followed by the addition of 3 ml chloroform. The mixture was left at room temperature for 3 min and centrifuged at 2,300 g for 20 min. The supernatant was transferred to a fresh tube and mixed with 7.5 ml isopropanol. The mixture was left at room temperature for 10 min and centrifuged at 2,300 g for 20 min. The pellet was dried and dissolved in 300 μl of RNase-free water. mRNA was purified from approximately 200 μg total RNA using an OligotexTM-dT30 mRNA Purification kit (Takara, Shiga, Japan) according to the manufacturer’s instructions. The library was prepared with TruSeq Stranded mRNA Library Prep (Illumina Inc., San Diego, CA, USA), and obtained the sequences with MiSeq (Illumina) according to the manufacturer’s instructions. Read number of each nucleotid was viewed with IGV [ 30 ]. (TIF)
format Still Image
author Natsuki Omae (10318504)
Yuka Sameshima-Yamashita (6292238)
Kazunori Ushimaru (3689119)
Hideaki Koike (410323)
Hiroko Kitamoto (6076307)
Tomotake Morita (526538)
author_facet Natsuki Omae (10318504)
Yuka Sameshima-Yamashita (6292238)
Kazunori Ushimaru (3689119)
Hideaki Koike (410323)
Hiroko Kitamoto (6076307)
Tomotake Morita (526538)
author_sort Natsuki Omae (10318504)
title Expression levels of the three candidate genes of PEP4 .
title_short Expression levels of the three candidate genes of PEP4 .
title_full Expression levels of the three candidate genes of PEP4 .
title_fullStr Expression levels of the three candidate genes of PEP4 .
title_full_unstemmed Expression levels of the three candidate genes of PEP4 .
title_sort expression levels of the three candidate genes of pep4 .
publishDate 2021
url https://doi.org/10.1371/journal.pone.0247462.s007
genre Antarc*
Antarctica
genre_facet Antarc*
Antarctica
op_relation https://figshare.com/articles/figure/Expression_levels_of_the_three_candidate_genes_of_i_PEP4_i_/14230969
doi:10.1371/journal.pone.0247462.s007
op_rights CC BY 4.0
op_rightsnorm CC-BY
op_doi https://doi.org/10.1371/journal.pone.0247462.s007
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