Molecular cloning and expression analysis of glutathione peroxidase and glutathione reductase from Gracilaria lemaneiformis under heat stress
Abstract Glutathione peroxidase (GPx) and glutathione reductase (GR) are key enzymes in the antioxidant defense systems of living organisms and protect organisms from environmental stresses. To investigate the mechanism of resistance to heat stress in the red alga Gracilaria lemaneiformis, the cDNA...
Ausführliche Beschreibung
Gespeichert in:
| Autor*in: |
Lu, Ning [verfasserIn] Ding, Yan [verfasserIn] Zang, Xiao-Nan [verfasserIn] Zhang, Xue-Cheng [verfasserIn] Chen, Hao [verfasserIn] Mu, Xiao-Sheng [verfasserIn] |
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| Format: |
E-Artikel |
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| Sprache: |
Englisch |
| Erschienen: |
2013 |
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| Schlagwörter: |
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| Übergeordnetes Werk: |
Enthalten in: Journal of applied phycology - Dordrecht [u.a.] : Springer Science + Business Media B.V, 1989, 25(2013), 6 vom: 23. März, Seite 1925-1931 |
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| Übergeordnetes Werk: |
volume:25 ; year:2013 ; number:6 ; day:23 ; month:03 ; pages:1925-1931 |
| Links: |
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| DOI / URN: |
10.1007/s10811-013-0020-9 |
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| Katalog-ID: |
SPR013470302 |
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| 245 | 1 | 0 | |a Molecular cloning and expression analysis of glutathione peroxidase and glutathione reductase from Gracilaria lemaneiformis under heat stress |
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| 520 | |a Abstract Glutathione peroxidase (GPx) and glutathione reductase (GR) are key enzymes in the antioxidant defense systems of living organisms and protect organisms from environmental stresses. To investigate the mechanism of resistance to heat stress in the red alga Gracilaria lemaneiformis, the cDNA sequences encoding glutathione peroxidase and glutathione reductase of two strains (wild type and heat-tolerant cultivar 981) of G. lemaneiformis were successfully cloned using reverse transcription PCR and rapid amplification cDNA ends techniques. cDNA encoding GPx has 930 nucleotides with an open reading frame (ORF) of 750 nucleotides, encoding 249 amino acid residues. cDNA encoding GR was 1,572 nucleotides with a 1,416-nucleotide ORF encoding 471 amino acids. No introns existed in genomic DNA of GPx and GR of G. lemaneiformis. Southern blotting indicated that there was only one copy of GPx and GR in both strains. Under heat stress, bioactivity and mRNA transcription levels of both GPx and GR were upregulated in cultivar 981 compared to those in the wild type. These results indicate that both GPx and GR may play important roles in the ability of G. lemaneiformis to resist high temperatures. | ||
| 650 | 4 | |a Expression analysis |7 (dpeaa)DE-He213 | |
| 650 | 4 | |a Gene cloning |7 (dpeaa)DE-He213 | |
| 650 | 4 | |a Glutathione peroxidase |7 (dpeaa)DE-He213 | |
| 650 | 4 | |a Glutathione reductase |7 (dpeaa)DE-He213 | |
| 650 | 4 | |a Rhodophyta |7 (dpeaa)DE-He213 | |
| 650 | 4 | |a Heat stress |7 (dpeaa)DE-He213 | |
| 700 | 1 | |a Ding, Yan |e verfasserin |4 aut | |
| 700 | 1 | |a Zang, Xiao-Nan |e verfasserin |4 aut | |
| 700 | 1 | |a Zhang, Xue-Cheng |e verfasserin |4 aut | |
| 700 | 1 | |a Chen, Hao |e verfasserin |4 aut | |
| 700 | 1 | |a Mu, Xiao-Sheng |e verfasserin |4 aut | |
| 773 | 0 | 8 | |i Enthalten in |t Journal of applied phycology |d Dordrecht [u.a.] : Springer Science + Business Media B.V, 1989 |g 25(2013), 6 vom: 23. März, Seite 1925-1931 |w (DE-627)270429980 |w (DE-600)1477703-4 |x 1573-5176 |7 nnns |
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| 912 | |a GBV_ILN_40 | ||
| 912 | |a GBV_ILN_60 | ||
| 912 | |a GBV_ILN_62 | ||
| 912 | |a GBV_ILN_63 | ||
| 912 | |a GBV_ILN_69 | ||
| 912 | |a GBV_ILN_70 | ||
| 912 | |a GBV_ILN_73 | ||
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| 912 | |a GBV_ILN_90 | ||
| 912 | |a GBV_ILN_95 | ||
| 912 | |a GBV_ILN_100 | ||
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| 912 | |a GBV_ILN_105 | ||
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| 912 | |a GBV_ILN_150 | ||
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| 912 | |a GBV_ILN_161 | ||
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| 912 | |a GBV_ILN_370 | ||
| 912 | |a GBV_ILN_381 | ||
| 912 | |a GBV_ILN_602 | ||
| 912 | |a GBV_ILN_636 | ||
| 912 | |a GBV_ILN_702 | ||
| 912 | |a GBV_ILN_2001 | ||
| 912 | |a GBV_ILN_2003 | ||
| 912 | |a GBV_ILN_2004 | ||
| 912 | |a GBV_ILN_2005 | ||
| 912 | |a GBV_ILN_2006 | ||
| 912 | |a GBV_ILN_2007 | ||
| 912 | |a GBV_ILN_2008 | ||
| 912 | |a GBV_ILN_2009 | ||
| 912 | |a GBV_ILN_2010 | ||
| 912 | |a GBV_ILN_2011 | ||
| 912 | |a GBV_ILN_2014 | ||
| 912 | |a GBV_ILN_2015 | ||
| 912 | |a GBV_ILN_2020 | ||
| 912 | |a GBV_ILN_2021 | ||
| 912 | |a GBV_ILN_2025 | ||
| 912 | |a GBV_ILN_2026 | ||
| 912 | |a GBV_ILN_2027 | ||
| 912 | |a GBV_ILN_2031 | ||
| 912 | |a GBV_ILN_2034 | ||
| 912 | |a GBV_ILN_2037 | ||
| 912 | |a GBV_ILN_2038 | ||
| 912 | |a GBV_ILN_2039 | ||
| 912 | |a GBV_ILN_2044 | ||
| 912 | |a GBV_ILN_2048 | ||
| 912 | |a GBV_ILN_2049 | ||
| 912 | |a GBV_ILN_2050 | ||
| 912 | |a GBV_ILN_2055 | ||
| 912 | |a GBV_ILN_2057 | ||
| 912 | |a GBV_ILN_2059 | ||
| 912 | |a GBV_ILN_2061 | ||
| 912 | |a GBV_ILN_2064 | ||
| 912 | |a GBV_ILN_2065 | ||
| 912 | |a GBV_ILN_2068 | ||
| 912 | |a GBV_ILN_2070 | ||
| 912 | |a GBV_ILN_2086 | ||
| 912 | |a GBV_ILN_2088 | ||
| 912 | |a GBV_ILN_2093 | ||
| 912 | |a GBV_ILN_2106 | ||
| 912 | |a GBV_ILN_2107 | ||
| 912 | |a GBV_ILN_2108 | ||
| 912 | |a GBV_ILN_2110 | ||
| 912 | |a GBV_ILN_2111 | ||
| 912 | |a GBV_ILN_2112 | ||
| 912 | |a GBV_ILN_2113 | ||
| 912 | |a GBV_ILN_2116 | ||
| 912 | |a GBV_ILN_2118 | ||
| 912 | |a GBV_ILN_2119 | ||
| 912 | |a GBV_ILN_2122 | ||
| 912 | |a GBV_ILN_2129 | ||
| 912 | |a GBV_ILN_2143 | ||
| 912 | |a GBV_ILN_2144 | ||
| 912 | |a GBV_ILN_2147 | ||
| 912 | |a GBV_ILN_2148 | ||
| 912 | |a GBV_ILN_2152 | ||
| 912 | |a GBV_ILN_2153 | ||
| 912 | |a GBV_ILN_2188 | ||
| 912 | |a GBV_ILN_2190 | ||
| 912 | |a GBV_ILN_2232 | ||
| 912 | |a GBV_ILN_2336 | ||
| 912 | |a GBV_ILN_2360 | ||
| 912 | |a GBV_ILN_2446 | ||
| 912 | |a GBV_ILN_2470 | ||
| 912 | |a GBV_ILN_2472 | ||
| 912 | |a GBV_ILN_2507 | ||
| 912 | |a GBV_ILN_2522 | ||
| 912 | |a GBV_ILN_2548 | ||
| 912 | |a GBV_ILN_4012 | ||
| 912 | |a GBV_ILN_4035 | ||
| 912 | |a GBV_ILN_4037 | ||
| 912 | |a GBV_ILN_4046 | ||
| 912 | |a GBV_ILN_4112 | ||
| 912 | |a GBV_ILN_4125 | ||
| 912 | |a GBV_ILN_4126 | ||
| 912 | |a GBV_ILN_4242 | ||
| 912 | |a GBV_ILN_4246 | ||
| 912 | |a GBV_ILN_4249 | ||
| 912 | |a GBV_ILN_4251 | ||
| 912 | |a GBV_ILN_4305 | ||
| 912 | |a GBV_ILN_4306 | ||
| 912 | |a GBV_ILN_4307 | ||
| 912 | |a GBV_ILN_4313 | ||
| 912 | |a GBV_ILN_4322 | ||
| 912 | |a GBV_ILN_4323 | ||
| 912 | |a GBV_ILN_4324 | ||
| 912 | |a GBV_ILN_4325 | ||
| 912 | |a GBV_ILN_4326 | ||
| 912 | |a GBV_ILN_4333 | ||
| 912 | |a GBV_ILN_4334 | ||
| 912 | |a GBV_ILN_4335 | ||
| 912 | |a GBV_ILN_4336 | ||
| 912 | |a GBV_ILN_4338 | ||
| 912 | |a GBV_ILN_4393 | ||
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10.1007/s10811-013-0020-9 doi (DE-627)SPR013470302 (SPR)s10811-013-0020-9-e DE-627 ger DE-627 rakwb eng 580 570 ASE 42.00 bkl Lu, Ning verfasserin aut Molecular cloning and expression analysis of glutathione peroxidase and glutathione reductase from Gracilaria lemaneiformis under heat stress 2013 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Glutathione peroxidase (GPx) and glutathione reductase (GR) are key enzymes in the antioxidant defense systems of living organisms and protect organisms from environmental stresses. To investigate the mechanism of resistance to heat stress in the red alga Gracilaria lemaneiformis, the cDNA sequences encoding glutathione peroxidase and glutathione reductase of two strains (wild type and heat-tolerant cultivar 981) of G. lemaneiformis were successfully cloned using reverse transcription PCR and rapid amplification cDNA ends techniques. cDNA encoding GPx has 930 nucleotides with an open reading frame (ORF) of 750 nucleotides, encoding 249 amino acid residues. cDNA encoding GR was 1,572 nucleotides with a 1,416-nucleotide ORF encoding 471 amino acids. No introns existed in genomic DNA of GPx and GR of G. lemaneiformis. Southern blotting indicated that there was only one copy of GPx and GR in both strains. Under heat stress, bioactivity and mRNA transcription levels of both GPx and GR were upregulated in cultivar 981 compared to those in the wild type. These results indicate that both GPx and GR may play important roles in the ability of G. lemaneiformis to resist high temperatures. Expression analysis (dpeaa)DE-He213 Gene cloning (dpeaa)DE-He213 Glutathione peroxidase (dpeaa)DE-He213 Glutathione reductase (dpeaa)DE-He213 Rhodophyta (dpeaa)DE-He213 Heat stress (dpeaa)DE-He213 Ding, Yan verfasserin aut Zang, Xiao-Nan verfasserin aut Zhang, Xue-Cheng verfasserin aut Chen, Hao verfasserin aut Mu, Xiao-Sheng verfasserin aut Enthalten in Journal of applied phycology Dordrecht [u.a.] : Springer Science + Business Media B.V, 1989 25(2013), 6 vom: 23. März, Seite 1925-1931 (DE-627)270429980 (DE-600)1477703-4 1573-5176 nnns volume:25 year:2013 number:6 day:23 month:03 pages:1925-1931 https://dx.doi.org/10.1007/s10811-013-0020-9 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_381 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2360 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 42.00 ASE AR 25 2013 6 23 03 1925-1931 |
| spelling |
10.1007/s10811-013-0020-9 doi (DE-627)SPR013470302 (SPR)s10811-013-0020-9-e DE-627 ger DE-627 rakwb eng 580 570 ASE 42.00 bkl Lu, Ning verfasserin aut Molecular cloning and expression analysis of glutathione peroxidase and glutathione reductase from Gracilaria lemaneiformis under heat stress 2013 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Glutathione peroxidase (GPx) and glutathione reductase (GR) are key enzymes in the antioxidant defense systems of living organisms and protect organisms from environmental stresses. To investigate the mechanism of resistance to heat stress in the red alga Gracilaria lemaneiformis, the cDNA sequences encoding glutathione peroxidase and glutathione reductase of two strains (wild type and heat-tolerant cultivar 981) of G. lemaneiformis were successfully cloned using reverse transcription PCR and rapid amplification cDNA ends techniques. cDNA encoding GPx has 930 nucleotides with an open reading frame (ORF) of 750 nucleotides, encoding 249 amino acid residues. cDNA encoding GR was 1,572 nucleotides with a 1,416-nucleotide ORF encoding 471 amino acids. No introns existed in genomic DNA of GPx and GR of G. lemaneiformis. Southern blotting indicated that there was only one copy of GPx and GR in both strains. Under heat stress, bioactivity and mRNA transcription levels of both GPx and GR were upregulated in cultivar 981 compared to those in the wild type. These results indicate that both GPx and GR may play important roles in the ability of G. lemaneiformis to resist high temperatures. Expression analysis (dpeaa)DE-He213 Gene cloning (dpeaa)DE-He213 Glutathione peroxidase (dpeaa)DE-He213 Glutathione reductase (dpeaa)DE-He213 Rhodophyta (dpeaa)DE-He213 Heat stress (dpeaa)DE-He213 Ding, Yan verfasserin aut Zang, Xiao-Nan verfasserin aut Zhang, Xue-Cheng verfasserin aut Chen, Hao verfasserin aut Mu, Xiao-Sheng verfasserin aut Enthalten in Journal of applied phycology Dordrecht [u.a.] : Springer Science + Business Media B.V, 1989 25(2013), 6 vom: 23. März, Seite 1925-1931 (DE-627)270429980 (DE-600)1477703-4 1573-5176 nnns volume:25 year:2013 number:6 day:23 month:03 pages:1925-1931 https://dx.doi.org/10.1007/s10811-013-0020-9 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_381 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2360 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 42.00 ASE AR 25 2013 6 23 03 1925-1931 |
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10.1007/s10811-013-0020-9 doi (DE-627)SPR013470302 (SPR)s10811-013-0020-9-e DE-627 ger DE-627 rakwb eng 580 570 ASE 42.00 bkl Lu, Ning verfasserin aut Molecular cloning and expression analysis of glutathione peroxidase and glutathione reductase from Gracilaria lemaneiformis under heat stress 2013 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Glutathione peroxidase (GPx) and glutathione reductase (GR) are key enzymes in the antioxidant defense systems of living organisms and protect organisms from environmental stresses. To investigate the mechanism of resistance to heat stress in the red alga Gracilaria lemaneiformis, the cDNA sequences encoding glutathione peroxidase and glutathione reductase of two strains (wild type and heat-tolerant cultivar 981) of G. lemaneiformis were successfully cloned using reverse transcription PCR and rapid amplification cDNA ends techniques. cDNA encoding GPx has 930 nucleotides with an open reading frame (ORF) of 750 nucleotides, encoding 249 amino acid residues. cDNA encoding GR was 1,572 nucleotides with a 1,416-nucleotide ORF encoding 471 amino acids. No introns existed in genomic DNA of GPx and GR of G. lemaneiformis. Southern blotting indicated that there was only one copy of GPx and GR in both strains. Under heat stress, bioactivity and mRNA transcription levels of both GPx and GR were upregulated in cultivar 981 compared to those in the wild type. These results indicate that both GPx and GR may play important roles in the ability of G. lemaneiformis to resist high temperatures. Expression analysis (dpeaa)DE-He213 Gene cloning (dpeaa)DE-He213 Glutathione peroxidase (dpeaa)DE-He213 Glutathione reductase (dpeaa)DE-He213 Rhodophyta (dpeaa)DE-He213 Heat stress (dpeaa)DE-He213 Ding, Yan verfasserin aut Zang, Xiao-Nan verfasserin aut Zhang, Xue-Cheng verfasserin aut Chen, Hao verfasserin aut Mu, Xiao-Sheng verfasserin aut Enthalten in Journal of applied phycology Dordrecht [u.a.] : Springer Science + Business Media B.V, 1989 25(2013), 6 vom: 23. März, Seite 1925-1931 (DE-627)270429980 (DE-600)1477703-4 1573-5176 nnns volume:25 year:2013 number:6 day:23 month:03 pages:1925-1931 https://dx.doi.org/10.1007/s10811-013-0020-9 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_381 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2360 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 42.00 ASE AR 25 2013 6 23 03 1925-1931 |
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10.1007/s10811-013-0020-9 doi (DE-627)SPR013470302 (SPR)s10811-013-0020-9-e DE-627 ger DE-627 rakwb eng 580 570 ASE 42.00 bkl Lu, Ning verfasserin aut Molecular cloning and expression analysis of glutathione peroxidase and glutathione reductase from Gracilaria lemaneiformis under heat stress 2013 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Glutathione peroxidase (GPx) and glutathione reductase (GR) are key enzymes in the antioxidant defense systems of living organisms and protect organisms from environmental stresses. To investigate the mechanism of resistance to heat stress in the red alga Gracilaria lemaneiformis, the cDNA sequences encoding glutathione peroxidase and glutathione reductase of two strains (wild type and heat-tolerant cultivar 981) of G. lemaneiformis were successfully cloned using reverse transcription PCR and rapid amplification cDNA ends techniques. cDNA encoding GPx has 930 nucleotides with an open reading frame (ORF) of 750 nucleotides, encoding 249 amino acid residues. cDNA encoding GR was 1,572 nucleotides with a 1,416-nucleotide ORF encoding 471 amino acids. No introns existed in genomic DNA of GPx and GR of G. lemaneiformis. Southern blotting indicated that there was only one copy of GPx and GR in both strains. Under heat stress, bioactivity and mRNA transcription levels of both GPx and GR were upregulated in cultivar 981 compared to those in the wild type. These results indicate that both GPx and GR may play important roles in the ability of G. lemaneiformis to resist high temperatures. Expression analysis (dpeaa)DE-He213 Gene cloning (dpeaa)DE-He213 Glutathione peroxidase (dpeaa)DE-He213 Glutathione reductase (dpeaa)DE-He213 Rhodophyta (dpeaa)DE-He213 Heat stress (dpeaa)DE-He213 Ding, Yan verfasserin aut Zang, Xiao-Nan verfasserin aut Zhang, Xue-Cheng verfasserin aut Chen, Hao verfasserin aut Mu, Xiao-Sheng verfasserin aut Enthalten in Journal of applied phycology Dordrecht [u.a.] : Springer Science + Business Media B.V, 1989 25(2013), 6 vom: 23. März, Seite 1925-1931 (DE-627)270429980 (DE-600)1477703-4 1573-5176 nnns volume:25 year:2013 number:6 day:23 month:03 pages:1925-1931 https://dx.doi.org/10.1007/s10811-013-0020-9 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_381 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2360 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 42.00 ASE AR 25 2013 6 23 03 1925-1931 |
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10.1007/s10811-013-0020-9 doi (DE-627)SPR013470302 (SPR)s10811-013-0020-9-e DE-627 ger DE-627 rakwb eng 580 570 ASE 42.00 bkl Lu, Ning verfasserin aut Molecular cloning and expression analysis of glutathione peroxidase and glutathione reductase from Gracilaria lemaneiformis under heat stress 2013 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract Glutathione peroxidase (GPx) and glutathione reductase (GR) are key enzymes in the antioxidant defense systems of living organisms and protect organisms from environmental stresses. To investigate the mechanism of resistance to heat stress in the red alga Gracilaria lemaneiformis, the cDNA sequences encoding glutathione peroxidase and glutathione reductase of two strains (wild type and heat-tolerant cultivar 981) of G. lemaneiformis were successfully cloned using reverse transcription PCR and rapid amplification cDNA ends techniques. cDNA encoding GPx has 930 nucleotides with an open reading frame (ORF) of 750 nucleotides, encoding 249 amino acid residues. cDNA encoding GR was 1,572 nucleotides with a 1,416-nucleotide ORF encoding 471 amino acids. No introns existed in genomic DNA of GPx and GR of G. lemaneiformis. Southern blotting indicated that there was only one copy of GPx and GR in both strains. Under heat stress, bioactivity and mRNA transcription levels of both GPx and GR were upregulated in cultivar 981 compared to those in the wild type. These results indicate that both GPx and GR may play important roles in the ability of G. lemaneiformis to resist high temperatures. Expression analysis (dpeaa)DE-He213 Gene cloning (dpeaa)DE-He213 Glutathione peroxidase (dpeaa)DE-He213 Glutathione reductase (dpeaa)DE-He213 Rhodophyta (dpeaa)DE-He213 Heat stress (dpeaa)DE-He213 Ding, Yan verfasserin aut Zang, Xiao-Nan verfasserin aut Zhang, Xue-Cheng verfasserin aut Chen, Hao verfasserin aut Mu, Xiao-Sheng verfasserin aut Enthalten in Journal of applied phycology Dordrecht [u.a.] : Springer Science + Business Media B.V, 1989 25(2013), 6 vom: 23. März, Seite 1925-1931 (DE-627)270429980 (DE-600)1477703-4 1573-5176 nnns volume:25 year:2013 number:6 day:23 month:03 pages:1925-1931 https://dx.doi.org/10.1007/s10811-013-0020-9 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_381 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2360 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 42.00 ASE AR 25 2013 6 23 03 1925-1931 |
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Enthalten in Journal of applied phycology 25(2013), 6 vom: 23. März, Seite 1925-1931 volume:25 year:2013 number:6 day:23 month:03 pages:1925-1931 |
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Expression analysis Gene cloning Glutathione peroxidase Glutathione reductase Rhodophyta Heat stress |
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Lu, Ning @@aut@@ Ding, Yan @@aut@@ Zang, Xiao-Nan @@aut@@ Zhang, Xue-Cheng @@aut@@ Chen, Hao @@aut@@ Mu, Xiao-Sheng @@aut@@ |
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Lu, Ning |
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Lu, Ning ddc 580 bkl 42.00 misc Expression analysis misc Gene cloning misc Glutathione peroxidase misc Glutathione reductase misc Rhodophyta misc Heat stress Molecular cloning and expression analysis of glutathione peroxidase and glutathione reductase from Gracilaria lemaneiformis under heat stress |
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580 570 ASE 42.00 bkl Molecular cloning and expression analysis of glutathione peroxidase and glutathione reductase from Gracilaria lemaneiformis under heat stress Expression analysis (dpeaa)DE-He213 Gene cloning (dpeaa)DE-He213 Glutathione peroxidase (dpeaa)DE-He213 Glutathione reductase (dpeaa)DE-He213 Rhodophyta (dpeaa)DE-He213 Heat stress (dpeaa)DE-He213 |
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ddc 580 bkl 42.00 misc Expression analysis misc Gene cloning misc Glutathione peroxidase misc Glutathione reductase misc Rhodophyta misc Heat stress |
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Molecular cloning and expression analysis of glutathione peroxidase and glutathione reductase from Gracilaria lemaneiformis under heat stress |
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Lu, Ning Ding, Yan Zang, Xiao-Nan Zhang, Xue-Cheng Chen, Hao Mu, Xiao-Sheng |
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Lu, Ning |
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molecular cloning and expression analysis of glutathione peroxidase and glutathione reductase from gracilaria lemaneiformis under heat stress |
| title_auth |
Molecular cloning and expression analysis of glutathione peroxidase and glutathione reductase from Gracilaria lemaneiformis under heat stress |
| abstract |
Abstract Glutathione peroxidase (GPx) and glutathione reductase (GR) are key enzymes in the antioxidant defense systems of living organisms and protect organisms from environmental stresses. To investigate the mechanism of resistance to heat stress in the red alga Gracilaria lemaneiformis, the cDNA sequences encoding glutathione peroxidase and glutathione reductase of two strains (wild type and heat-tolerant cultivar 981) of G. lemaneiformis were successfully cloned using reverse transcription PCR and rapid amplification cDNA ends techniques. cDNA encoding GPx has 930 nucleotides with an open reading frame (ORF) of 750 nucleotides, encoding 249 amino acid residues. cDNA encoding GR was 1,572 nucleotides with a 1,416-nucleotide ORF encoding 471 amino acids. No introns existed in genomic DNA of GPx and GR of G. lemaneiformis. Southern blotting indicated that there was only one copy of GPx and GR in both strains. Under heat stress, bioactivity and mRNA transcription levels of both GPx and GR were upregulated in cultivar 981 compared to those in the wild type. These results indicate that both GPx and GR may play important roles in the ability of G. lemaneiformis to resist high temperatures. |
| abstractGer |
Abstract Glutathione peroxidase (GPx) and glutathione reductase (GR) are key enzymes in the antioxidant defense systems of living organisms and protect organisms from environmental stresses. To investigate the mechanism of resistance to heat stress in the red alga Gracilaria lemaneiformis, the cDNA sequences encoding glutathione peroxidase and glutathione reductase of two strains (wild type and heat-tolerant cultivar 981) of G. lemaneiformis were successfully cloned using reverse transcription PCR and rapid amplification cDNA ends techniques. cDNA encoding GPx has 930 nucleotides with an open reading frame (ORF) of 750 nucleotides, encoding 249 amino acid residues. cDNA encoding GR was 1,572 nucleotides with a 1,416-nucleotide ORF encoding 471 amino acids. No introns existed in genomic DNA of GPx and GR of G. lemaneiformis. Southern blotting indicated that there was only one copy of GPx and GR in both strains. Under heat stress, bioactivity and mRNA transcription levels of both GPx and GR were upregulated in cultivar 981 compared to those in the wild type. These results indicate that both GPx and GR may play important roles in the ability of G. lemaneiformis to resist high temperatures. |
| abstract_unstemmed |
Abstract Glutathione peroxidase (GPx) and glutathione reductase (GR) are key enzymes in the antioxidant defense systems of living organisms and protect organisms from environmental stresses. To investigate the mechanism of resistance to heat stress in the red alga Gracilaria lemaneiformis, the cDNA sequences encoding glutathione peroxidase and glutathione reductase of two strains (wild type and heat-tolerant cultivar 981) of G. lemaneiformis were successfully cloned using reverse transcription PCR and rapid amplification cDNA ends techniques. cDNA encoding GPx has 930 nucleotides with an open reading frame (ORF) of 750 nucleotides, encoding 249 amino acid residues. cDNA encoding GR was 1,572 nucleotides with a 1,416-nucleotide ORF encoding 471 amino acids. No introns existed in genomic DNA of GPx and GR of G. lemaneiformis. Southern blotting indicated that there was only one copy of GPx and GR in both strains. Under heat stress, bioactivity and mRNA transcription levels of both GPx and GR were upregulated in cultivar 981 compared to those in the wild type. These results indicate that both GPx and GR may play important roles in the ability of G. lemaneiformis to resist high temperatures. |
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Molecular cloning and expression analysis of glutathione peroxidase and glutathione reductase from Gracilaria lemaneiformis under heat stress |
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https://dx.doi.org/10.1007/s10811-013-0020-9 |
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Ding, Yan Zang, Xiao-Nan Zhang, Xue-Cheng Chen, Hao Mu, Xiao-Sheng |
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| score |
7.3995686 |