Immunolocalization and structural variations of xylan in differentiating earlywood tracheid cell walls of Cryptomeria japonica
Abstract We investigated the spatial and temporal distribution of xylans in the cell walls of differentiating earlywood tracheids of Cryptomeria japonica using two different types of monoclonal antibodies (LM10 and LM11) combined with immunomicroscopy. Xylans were first deposited in the corner of th...
Ausführliche Beschreibung
Gespeichert in:
| Autor*in: |
Kim, Jong Sik [verfasserIn] Awano, Tatsuya [verfasserIn] Yoshinaga, Arata [verfasserIn] Takabe, Keiji [verfasserIn] |
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| Format: |
E-Artikel |
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| Sprache: |
Englisch |
| Erschienen: |
2010 |
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| Schlagwörter: |
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| Übergeordnetes Werk: |
Enthalten in: Planta - Berlin : Springer, 1925, 232(2010), 4 vom: 14. Juli, Seite 817-824 |
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| Übergeordnetes Werk: |
volume:232 ; year:2010 ; number:4 ; day:14 ; month:07 ; pages:817-824 |
| Links: |
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| DOI / URN: |
10.1007/s00425-010-1225-7 |
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| Katalog-ID: |
SPR005660300 |
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| 245 | 1 | 0 | |a Immunolocalization and structural variations of xylan in differentiating earlywood tracheid cell walls of Cryptomeria japonica |
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| 520 | |a Abstract We investigated the spatial and temporal distribution of xylans in the cell walls of differentiating earlywood tracheids of Cryptomeria japonica using two different types of monoclonal antibodies (LM10 and LM11) combined with immunomicroscopy. Xylans were first deposited in the corner of the $ S_{1} $ layer in the early stages of $ S_{1} $ formation in tracheids. Cell corner middle lamella also showed strong xylan labeling from the early stage of cell wall formation. During secondary cell wall formation, the innermost layer and the boundary between the $ S_{1} $ and $ S_{2} $ layers ($ S_{1} $/$ S_{2} $ region) showed weaker labeling than other parts of the cell wall. However, mature tracheids had an almost uniform distribution of xylans throughout the entire cell wall. Xylan localization labeled with LM10 antibody was stronger in the outer $ S_{2} $ layer than in the inner layer, whereas xylans labeled with LM11 antibody were almost uniformly distributed in the $ S_{2} $ layer. In addition, the LM10 antibody showed almost no xylan labeling in the $ S_{1} $/$ S_{2} $ region, whereas the LM11 antibody revealed strong xylan labeling in the $ S_{1} $/$ S_{2} $ region. These findings suggest that structurally different types of xylans may be deposited in the tracheid cell wall depending on the developmental stage of, or location in, the cell wall. Our study also indicates that deposition of xylans in the early stages of tracheid cell wall formation may be spatially consistent with the early stage of lignin deposition in the tracheid cell wall. | ||
| 650 | 4 | |a Immunolocalization |7 (dpeaa)DE-He213 | |
| 650 | 4 | |a LM10 antibody |7 (dpeaa)DE-He213 | |
| 650 | 4 | |a LM11 antibody |7 (dpeaa)DE-He213 | |
| 650 | 4 | |a Xylan |7 (dpeaa)DE-He213 | |
| 700 | 1 | |a Awano, Tatsuya |e verfasserin |4 aut | |
| 700 | 1 | |a Yoshinaga, Arata |e verfasserin |4 aut | |
| 700 | 1 | |a Takabe, Keiji |e verfasserin |4 aut | |
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10.1007/s00425-010-1225-7 doi (DE-627)SPR005660300 (SPR)s00425-010-1225-7-e DE-627 ger DE-627 rakwb eng 580 ASE 42.38 bkl Kim, Jong Sik verfasserin aut Immunolocalization and structural variations of xylan in differentiating earlywood tracheid cell walls of Cryptomeria japonica 2010 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract We investigated the spatial and temporal distribution of xylans in the cell walls of differentiating earlywood tracheids of Cryptomeria japonica using two different types of monoclonal antibodies (LM10 and LM11) combined with immunomicroscopy. Xylans were first deposited in the corner of the $ S_{1} $ layer in the early stages of $ S_{1} $ formation in tracheids. Cell corner middle lamella also showed strong xylan labeling from the early stage of cell wall formation. During secondary cell wall formation, the innermost layer and the boundary between the $ S_{1} $ and $ S_{2} $ layers ($ S_{1} $/$ S_{2} $ region) showed weaker labeling than other parts of the cell wall. However, mature tracheids had an almost uniform distribution of xylans throughout the entire cell wall. Xylan localization labeled with LM10 antibody was stronger in the outer $ S_{2} $ layer than in the inner layer, whereas xylans labeled with LM11 antibody were almost uniformly distributed in the $ S_{2} $ layer. In addition, the LM10 antibody showed almost no xylan labeling in the $ S_{1} $/$ S_{2} $ region, whereas the LM11 antibody revealed strong xylan labeling in the $ S_{1} $/$ S_{2} $ region. These findings suggest that structurally different types of xylans may be deposited in the tracheid cell wall depending on the developmental stage of, or location in, the cell wall. Our study also indicates that deposition of xylans in the early stages of tracheid cell wall formation may be spatially consistent with the early stage of lignin deposition in the tracheid cell wall. Immunolocalization (dpeaa)DE-He213 LM10 antibody (dpeaa)DE-He213 LM11 antibody (dpeaa)DE-He213 Xylan (dpeaa)DE-He213 Awano, Tatsuya verfasserin aut Yoshinaga, Arata verfasserin aut Takabe, Keiji verfasserin aut Enthalten in Planta Berlin : Springer, 1925 232(2010), 4 vom: 14. Juli, Seite 817-824 (DE-627)254639100 (DE-600)1463030-8 1432-2048 nnns volume:232 year:2010 number:4 day:14 month:07 pages:817-824 https://dx.doi.org/10.1007/s00425-010-1225-7 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_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 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_267 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_374 GBV_ILN_602 GBV_ILN_636 GBV_ILN_647 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_2018 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_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_2946 GBV_ILN_2949 GBV_ILN_2951 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_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4346 GBV_ILN_4393 GBV_ILN_4700 42.38 ASE AR 232 2010 4 14 07 817-824 |
| spelling |
10.1007/s00425-010-1225-7 doi (DE-627)SPR005660300 (SPR)s00425-010-1225-7-e DE-627 ger DE-627 rakwb eng 580 ASE 42.38 bkl Kim, Jong Sik verfasserin aut Immunolocalization and structural variations of xylan in differentiating earlywood tracheid cell walls of Cryptomeria japonica 2010 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract We investigated the spatial and temporal distribution of xylans in the cell walls of differentiating earlywood tracheids of Cryptomeria japonica using two different types of monoclonal antibodies (LM10 and LM11) combined with immunomicroscopy. Xylans were first deposited in the corner of the $ S_{1} $ layer in the early stages of $ S_{1} $ formation in tracheids. Cell corner middle lamella also showed strong xylan labeling from the early stage of cell wall formation. During secondary cell wall formation, the innermost layer and the boundary between the $ S_{1} $ and $ S_{2} $ layers ($ S_{1} $/$ S_{2} $ region) showed weaker labeling than other parts of the cell wall. However, mature tracheids had an almost uniform distribution of xylans throughout the entire cell wall. Xylan localization labeled with LM10 antibody was stronger in the outer $ S_{2} $ layer than in the inner layer, whereas xylans labeled with LM11 antibody were almost uniformly distributed in the $ S_{2} $ layer. In addition, the LM10 antibody showed almost no xylan labeling in the $ S_{1} $/$ S_{2} $ region, whereas the LM11 antibody revealed strong xylan labeling in the $ S_{1} $/$ S_{2} $ region. These findings suggest that structurally different types of xylans may be deposited in the tracheid cell wall depending on the developmental stage of, or location in, the cell wall. Our study also indicates that deposition of xylans in the early stages of tracheid cell wall formation may be spatially consistent with the early stage of lignin deposition in the tracheid cell wall. Immunolocalization (dpeaa)DE-He213 LM10 antibody (dpeaa)DE-He213 LM11 antibody (dpeaa)DE-He213 Xylan (dpeaa)DE-He213 Awano, Tatsuya verfasserin aut Yoshinaga, Arata verfasserin aut Takabe, Keiji verfasserin aut Enthalten in Planta Berlin : Springer, 1925 232(2010), 4 vom: 14. Juli, Seite 817-824 (DE-627)254639100 (DE-600)1463030-8 1432-2048 nnns volume:232 year:2010 number:4 day:14 month:07 pages:817-824 https://dx.doi.org/10.1007/s00425-010-1225-7 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_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 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_267 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_374 GBV_ILN_602 GBV_ILN_636 GBV_ILN_647 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_2018 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_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_2946 GBV_ILN_2949 GBV_ILN_2951 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_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4346 GBV_ILN_4393 GBV_ILN_4700 42.38 ASE AR 232 2010 4 14 07 817-824 |
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10.1007/s00425-010-1225-7 doi (DE-627)SPR005660300 (SPR)s00425-010-1225-7-e DE-627 ger DE-627 rakwb eng 580 ASE 42.38 bkl Kim, Jong Sik verfasserin aut Immunolocalization and structural variations of xylan in differentiating earlywood tracheid cell walls of Cryptomeria japonica 2010 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract We investigated the spatial and temporal distribution of xylans in the cell walls of differentiating earlywood tracheids of Cryptomeria japonica using two different types of monoclonal antibodies (LM10 and LM11) combined with immunomicroscopy. Xylans were first deposited in the corner of the $ S_{1} $ layer in the early stages of $ S_{1} $ formation in tracheids. Cell corner middle lamella also showed strong xylan labeling from the early stage of cell wall formation. During secondary cell wall formation, the innermost layer and the boundary between the $ S_{1} $ and $ S_{2} $ layers ($ S_{1} $/$ S_{2} $ region) showed weaker labeling than other parts of the cell wall. However, mature tracheids had an almost uniform distribution of xylans throughout the entire cell wall. Xylan localization labeled with LM10 antibody was stronger in the outer $ S_{2} $ layer than in the inner layer, whereas xylans labeled with LM11 antibody were almost uniformly distributed in the $ S_{2} $ layer. In addition, the LM10 antibody showed almost no xylan labeling in the $ S_{1} $/$ S_{2} $ region, whereas the LM11 antibody revealed strong xylan labeling in the $ S_{1} $/$ S_{2} $ region. These findings suggest that structurally different types of xylans may be deposited in the tracheid cell wall depending on the developmental stage of, or location in, the cell wall. Our study also indicates that deposition of xylans in the early stages of tracheid cell wall formation may be spatially consistent with the early stage of lignin deposition in the tracheid cell wall. Immunolocalization (dpeaa)DE-He213 LM10 antibody (dpeaa)DE-He213 LM11 antibody (dpeaa)DE-He213 Xylan (dpeaa)DE-He213 Awano, Tatsuya verfasserin aut Yoshinaga, Arata verfasserin aut Takabe, Keiji verfasserin aut Enthalten in Planta Berlin : Springer, 1925 232(2010), 4 vom: 14. Juli, Seite 817-824 (DE-627)254639100 (DE-600)1463030-8 1432-2048 nnns volume:232 year:2010 number:4 day:14 month:07 pages:817-824 https://dx.doi.org/10.1007/s00425-010-1225-7 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_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 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_267 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_374 GBV_ILN_602 GBV_ILN_636 GBV_ILN_647 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_2018 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_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_2946 GBV_ILN_2949 GBV_ILN_2951 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_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4346 GBV_ILN_4393 GBV_ILN_4700 42.38 ASE AR 232 2010 4 14 07 817-824 |
| allfieldsGer |
10.1007/s00425-010-1225-7 doi (DE-627)SPR005660300 (SPR)s00425-010-1225-7-e DE-627 ger DE-627 rakwb eng 580 ASE 42.38 bkl Kim, Jong Sik verfasserin aut Immunolocalization and structural variations of xylan in differentiating earlywood tracheid cell walls of Cryptomeria japonica 2010 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract We investigated the spatial and temporal distribution of xylans in the cell walls of differentiating earlywood tracheids of Cryptomeria japonica using two different types of monoclonal antibodies (LM10 and LM11) combined with immunomicroscopy. Xylans were first deposited in the corner of the $ S_{1} $ layer in the early stages of $ S_{1} $ formation in tracheids. Cell corner middle lamella also showed strong xylan labeling from the early stage of cell wall formation. During secondary cell wall formation, the innermost layer and the boundary between the $ S_{1} $ and $ S_{2} $ layers ($ S_{1} $/$ S_{2} $ region) showed weaker labeling than other parts of the cell wall. However, mature tracheids had an almost uniform distribution of xylans throughout the entire cell wall. Xylan localization labeled with LM10 antibody was stronger in the outer $ S_{2} $ layer than in the inner layer, whereas xylans labeled with LM11 antibody were almost uniformly distributed in the $ S_{2} $ layer. In addition, the LM10 antibody showed almost no xylan labeling in the $ S_{1} $/$ S_{2} $ region, whereas the LM11 antibody revealed strong xylan labeling in the $ S_{1} $/$ S_{2} $ region. These findings suggest that structurally different types of xylans may be deposited in the tracheid cell wall depending on the developmental stage of, or location in, the cell wall. Our study also indicates that deposition of xylans in the early stages of tracheid cell wall formation may be spatially consistent with the early stage of lignin deposition in the tracheid cell wall. Immunolocalization (dpeaa)DE-He213 LM10 antibody (dpeaa)DE-He213 LM11 antibody (dpeaa)DE-He213 Xylan (dpeaa)DE-He213 Awano, Tatsuya verfasserin aut Yoshinaga, Arata verfasserin aut Takabe, Keiji verfasserin aut Enthalten in Planta Berlin : Springer, 1925 232(2010), 4 vom: 14. Juli, Seite 817-824 (DE-627)254639100 (DE-600)1463030-8 1432-2048 nnns volume:232 year:2010 number:4 day:14 month:07 pages:817-824 https://dx.doi.org/10.1007/s00425-010-1225-7 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_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 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_267 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_374 GBV_ILN_602 GBV_ILN_636 GBV_ILN_647 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_2018 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_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_2946 GBV_ILN_2949 GBV_ILN_2951 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_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4346 GBV_ILN_4393 GBV_ILN_4700 42.38 ASE AR 232 2010 4 14 07 817-824 |
| allfieldsSound |
10.1007/s00425-010-1225-7 doi (DE-627)SPR005660300 (SPR)s00425-010-1225-7-e DE-627 ger DE-627 rakwb eng 580 ASE 42.38 bkl Kim, Jong Sik verfasserin aut Immunolocalization and structural variations of xylan in differentiating earlywood tracheid cell walls of Cryptomeria japonica 2010 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Abstract We investigated the spatial and temporal distribution of xylans in the cell walls of differentiating earlywood tracheids of Cryptomeria japonica using two different types of monoclonal antibodies (LM10 and LM11) combined with immunomicroscopy. Xylans were first deposited in the corner of the $ S_{1} $ layer in the early stages of $ S_{1} $ formation in tracheids. Cell corner middle lamella also showed strong xylan labeling from the early stage of cell wall formation. During secondary cell wall formation, the innermost layer and the boundary between the $ S_{1} $ and $ S_{2} $ layers ($ S_{1} $/$ S_{2} $ region) showed weaker labeling than other parts of the cell wall. However, mature tracheids had an almost uniform distribution of xylans throughout the entire cell wall. Xylan localization labeled with LM10 antibody was stronger in the outer $ S_{2} $ layer than in the inner layer, whereas xylans labeled with LM11 antibody were almost uniformly distributed in the $ S_{2} $ layer. In addition, the LM10 antibody showed almost no xylan labeling in the $ S_{1} $/$ S_{2} $ region, whereas the LM11 antibody revealed strong xylan labeling in the $ S_{1} $/$ S_{2} $ region. These findings suggest that structurally different types of xylans may be deposited in the tracheid cell wall depending on the developmental stage of, or location in, the cell wall. Our study also indicates that deposition of xylans in the early stages of tracheid cell wall formation may be spatially consistent with the early stage of lignin deposition in the tracheid cell wall. Immunolocalization (dpeaa)DE-He213 LM10 antibody (dpeaa)DE-He213 LM11 antibody (dpeaa)DE-He213 Xylan (dpeaa)DE-He213 Awano, Tatsuya verfasserin aut Yoshinaga, Arata verfasserin aut Takabe, Keiji verfasserin aut Enthalten in Planta Berlin : Springer, 1925 232(2010), 4 vom: 14. Juli, Seite 817-824 (DE-627)254639100 (DE-600)1463030-8 1432-2048 nnns volume:232 year:2010 number:4 day:14 month:07 pages:817-824 https://dx.doi.org/10.1007/s00425-010-1225-7 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_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 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_267 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_374 GBV_ILN_602 GBV_ILN_636 GBV_ILN_647 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_2018 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_2446 GBV_ILN_2470 GBV_ILN_2472 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_2946 GBV_ILN_2949 GBV_ILN_2951 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_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4346 GBV_ILN_4393 GBV_ILN_4700 42.38 ASE AR 232 2010 4 14 07 817-824 |
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English |
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Enthalten in Planta 232(2010), 4 vom: 14. Juli, Seite 817-824 volume:232 year:2010 number:4 day:14 month:07 pages:817-824 |
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Enthalten in Planta 232(2010), 4 vom: 14. Juli, Seite 817-824 volume:232 year:2010 number:4 day:14 month:07 pages:817-824 |
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Article |
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findex.gbv.de |
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Immunolocalization LM10 antibody LM11 antibody Xylan |
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Kim, Jong Sik @@aut@@ Awano, Tatsuya @@aut@@ Yoshinaga, Arata @@aut@@ Takabe, Keiji @@aut@@ |
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2010-07-14T00:00:00Z |
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Xylans were first deposited in the corner of the $ S_{1} $ layer in the early stages of $ S_{1} $ formation in tracheids. Cell corner middle lamella also showed strong xylan labeling from the early stage of cell wall formation. During secondary cell wall formation, the innermost layer and the boundary between the $ S_{1} $ and $ S_{2} $ layers ($ S_{1} $/$ S_{2} $ region) showed weaker labeling than other parts of the cell wall. However, mature tracheids had an almost uniform distribution of xylans throughout the entire cell wall. Xylan localization labeled with LM10 antibody was stronger in the outer $ S_{2} $ layer than in the inner layer, whereas xylans labeled with LM11 antibody were almost uniformly distributed in the $ S_{2} $ layer. In addition, the LM10 antibody showed almost no xylan labeling in the $ S_{1} $/$ S_{2} $ region, whereas the LM11 antibody revealed strong xylan labeling in the $ S_{1} $/$ S_{2} $ region. These findings suggest that structurally different types of xylans may be deposited in the tracheid cell wall depending on the developmental stage of, or location in, the cell wall. Our study also indicates that deposition of xylans in the early stages of tracheid cell wall formation may be spatially consistent with the early stage of lignin deposition in the tracheid cell wall.</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Immunolocalization</subfield><subfield code="7">(dpeaa)DE-He213</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">LM10 antibody</subfield><subfield code="7">(dpeaa)DE-He213</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">LM11 antibody</subfield><subfield code="7">(dpeaa)DE-He213</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Xylan</subfield><subfield code="7">(dpeaa)DE-He213</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Awano, Tatsuya</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Yoshinaga, Arata</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Takabe, Keiji</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="773" ind1="0" ind2="8"><subfield code="i">Enthalten in</subfield><subfield code="t">Planta</subfield><subfield code="d">Berlin : Springer, 1925</subfield><subfield code="g">232(2010), 4 vom: 14. 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Kim, Jong Sik |
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Kim, Jong Sik ddc 580 bkl 42.38 misc Immunolocalization misc LM10 antibody misc LM11 antibody misc Xylan Immunolocalization and structural variations of xylan in differentiating earlywood tracheid cell walls of Cryptomeria japonica |
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580 ASE 42.38 bkl Immunolocalization and structural variations of xylan in differentiating earlywood tracheid cell walls of Cryptomeria japonica Immunolocalization (dpeaa)DE-He213 LM10 antibody (dpeaa)DE-He213 LM11 antibody (dpeaa)DE-He213 Xylan (dpeaa)DE-He213 |
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ddc 580 bkl 42.38 misc Immunolocalization misc LM10 antibody misc LM11 antibody misc Xylan |
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Immunolocalization and structural variations of xylan in differentiating earlywood tracheid cell walls of Cryptomeria japonica |
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Immunolocalization and structural variations of xylan in differentiating earlywood tracheid cell walls of Cryptomeria japonica |
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Kim, Jong Sik Awano, Tatsuya Yoshinaga, Arata Takabe, Keiji |
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Elektronische Aufsätze |
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Kim, Jong Sik |
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immunolocalization and structural variations of xylan in differentiating earlywood tracheid cell walls of cryptomeria japonica |
| title_auth |
Immunolocalization and structural variations of xylan in differentiating earlywood tracheid cell walls of Cryptomeria japonica |
| abstract |
Abstract We investigated the spatial and temporal distribution of xylans in the cell walls of differentiating earlywood tracheids of Cryptomeria japonica using two different types of monoclonal antibodies (LM10 and LM11) combined with immunomicroscopy. Xylans were first deposited in the corner of the $ S_{1} $ layer in the early stages of $ S_{1} $ formation in tracheids. Cell corner middle lamella also showed strong xylan labeling from the early stage of cell wall formation. During secondary cell wall formation, the innermost layer and the boundary between the $ S_{1} $ and $ S_{2} $ layers ($ S_{1} $/$ S_{2} $ region) showed weaker labeling than other parts of the cell wall. However, mature tracheids had an almost uniform distribution of xylans throughout the entire cell wall. Xylan localization labeled with LM10 antibody was stronger in the outer $ S_{2} $ layer than in the inner layer, whereas xylans labeled with LM11 antibody were almost uniformly distributed in the $ S_{2} $ layer. In addition, the LM10 antibody showed almost no xylan labeling in the $ S_{1} $/$ S_{2} $ region, whereas the LM11 antibody revealed strong xylan labeling in the $ S_{1} $/$ S_{2} $ region. These findings suggest that structurally different types of xylans may be deposited in the tracheid cell wall depending on the developmental stage of, or location in, the cell wall. Our study also indicates that deposition of xylans in the early stages of tracheid cell wall formation may be spatially consistent with the early stage of lignin deposition in the tracheid cell wall. |
| abstractGer |
Abstract We investigated the spatial and temporal distribution of xylans in the cell walls of differentiating earlywood tracheids of Cryptomeria japonica using two different types of monoclonal antibodies (LM10 and LM11) combined with immunomicroscopy. Xylans were first deposited in the corner of the $ S_{1} $ layer in the early stages of $ S_{1} $ formation in tracheids. Cell corner middle lamella also showed strong xylan labeling from the early stage of cell wall formation. During secondary cell wall formation, the innermost layer and the boundary between the $ S_{1} $ and $ S_{2} $ layers ($ S_{1} $/$ S_{2} $ region) showed weaker labeling than other parts of the cell wall. However, mature tracheids had an almost uniform distribution of xylans throughout the entire cell wall. Xylan localization labeled with LM10 antibody was stronger in the outer $ S_{2} $ layer than in the inner layer, whereas xylans labeled with LM11 antibody were almost uniformly distributed in the $ S_{2} $ layer. In addition, the LM10 antibody showed almost no xylan labeling in the $ S_{1} $/$ S_{2} $ region, whereas the LM11 antibody revealed strong xylan labeling in the $ S_{1} $/$ S_{2} $ region. These findings suggest that structurally different types of xylans may be deposited in the tracheid cell wall depending on the developmental stage of, or location in, the cell wall. Our study also indicates that deposition of xylans in the early stages of tracheid cell wall formation may be spatially consistent with the early stage of lignin deposition in the tracheid cell wall. |
| abstract_unstemmed |
Abstract We investigated the spatial and temporal distribution of xylans in the cell walls of differentiating earlywood tracheids of Cryptomeria japonica using two different types of monoclonal antibodies (LM10 and LM11) combined with immunomicroscopy. Xylans were first deposited in the corner of the $ S_{1} $ layer in the early stages of $ S_{1} $ formation in tracheids. Cell corner middle lamella also showed strong xylan labeling from the early stage of cell wall formation. During secondary cell wall formation, the innermost layer and the boundary between the $ S_{1} $ and $ S_{2} $ layers ($ S_{1} $/$ S_{2} $ region) showed weaker labeling than other parts of the cell wall. However, mature tracheids had an almost uniform distribution of xylans throughout the entire cell wall. Xylan localization labeled with LM10 antibody was stronger in the outer $ S_{2} $ layer than in the inner layer, whereas xylans labeled with LM11 antibody were almost uniformly distributed in the $ S_{2} $ layer. In addition, the LM10 antibody showed almost no xylan labeling in the $ S_{1} $/$ S_{2} $ region, whereas the LM11 antibody revealed strong xylan labeling in the $ S_{1} $/$ S_{2} $ region. These findings suggest that structurally different types of xylans may be deposited in the tracheid cell wall depending on the developmental stage of, or location in, the cell wall. Our study also indicates that deposition of xylans in the early stages of tracheid cell wall formation may be spatially consistent with the early stage of lignin deposition in the tracheid cell wall. |
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Immunolocalization and structural variations of xylan in differentiating earlywood tracheid cell walls of Cryptomeria japonica |
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Awano, Tatsuya Yoshinaga, Arata Takabe, Keiji |
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2024-07-03T17:51:02.077Z |
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| score |
7.4007673 |