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Title: New isoforms and assembly of glutamine synthetase in the leaf of wheat ( Triticum aestivum L.)

Abstract

Glutamine synthetase (GS; EC 6.3.1.2) plays a crucial role in the assimilation and re-assimilation of ammonia derived from a wide variety of metabolic processes during plant growth and development. Here, three developmentally regulated isoforms of GS holoenzyme in the leaf of wheat ( Triticum aestivum L.) seedlings are described using native-PAGE with a transferase activity assay. The isoforms showed different mobilities in gels, with GSII>GSIII>GSI. The cytosolic GSI was composed of three subunits, GS1, GSr1, and GSr2, with the same molecular weight (39.2kDa), but different pI values. GSI appeared at leaf emergence and was active throughout the leaf lifespan. GSII and GSIII, both located in the chloroplast, were each composed of a single 42.1kDa subunit with different pI values. GSII was active mainly in green leaves, while GSIII showed brief but higher activity in green leaves grown under field conditions. LC-MS/MS experiments revealed that GSII and GSIII have the same amino acid sequence, but GSII has more modification sites. With a modified blue native electrophoresis (BNE) technique and in-gel catalytic activity analysis, only two GS isoforms were observed: one cytosolic and one chloroplastic. Mass calibrations on BNE gels showed that the cytosolic GS1 holoenzyme was ~490kDa and likely a dodecamer,more » and the chloroplastic GS2 holoenzyme was ~240kDa and likely a hexamer. Lastly, our experimental data suggest that the activity of GS isoforms in wheat is regulated by subcellular localization, assembly, and modification to achieve their roles during plant development.« less

Authors:
 [1];  [1];  [2];  [1];  [2]
  1. Henan Agriculture Univ., Zhengzhou (China)
  2. Univ. of California, Davis, CA (United States)
Publication Date:
Research Org.:
Univ. of California, Davis, CA (United States)
Sponsoring Org.:
USDOE Office of Science (SC), Basic Energy Sciences (BES) (SC-22); USDOE Office of Science (SC), Basic Energy Sciences (BES) (SC-22). Chemical Sciences, Geosciences & Biosciences Division
OSTI Identifier:
1343290
Alternate Identifier(s):
OSTI ID: 1439060
Grant/Contract Number:  
FG02-03ER15405
Resource Type:
Journal Article: Accepted Manuscript
Journal Name:
Journal of Experimental Botany
Additional Journal Information:
Journal Volume: 66; Journal Issue: 21; Journal ID: ISSN 0022-0957
Publisher:
Oxford University Press
Country of Publication:
United States
Language:
English
Subject:
60 APPLIED LIFE SCIENCES; assembly; enzyme isoform; glutamine synthetase; nitrogen; protein modification; wheat

Citation Formats

Wang, Xiaochun, Wei, Yihao, Shi, Lanxin, Ma, Xinming, and Theg, Steven M. New isoforms and assembly of glutamine synthetase in the leaf of wheat (Triticum aestivum L.). United States: N. p., 2015. Web. doi:10.1093/jxb/erv388.
Wang, Xiaochun, Wei, Yihao, Shi, Lanxin, Ma, Xinming, & Theg, Steven M. New isoforms and assembly of glutamine synthetase in the leaf of wheat (Triticum aestivum L.). United States. doi:10.1093/jxb/erv388.
Wang, Xiaochun, Wei, Yihao, Shi, Lanxin, Ma, Xinming, and Theg, Steven M. Mon . "New isoforms and assembly of glutamine synthetase in the leaf of wheat (Triticum aestivum L.)". United States. doi:10.1093/jxb/erv388. https://www.osti.gov/servlets/purl/1343290.
@article{osti_1343290,
title = {New isoforms and assembly of glutamine synthetase in the leaf of wheat (Triticum aestivum L.)},
author = {Wang, Xiaochun and Wei, Yihao and Shi, Lanxin and Ma, Xinming and Theg, Steven M.},
abstractNote = {Glutamine synthetase (GS; EC 6.3.1.2) plays a crucial role in the assimilation and re-assimilation of ammonia derived from a wide variety of metabolic processes during plant growth and development. Here, three developmentally regulated isoforms of GS holoenzyme in the leaf of wheat (Triticum aestivum L.) seedlings are described using native-PAGE with a transferase activity assay. The isoforms showed different mobilities in gels, with GSII>GSIII>GSI. The cytosolic GSI was composed of three subunits, GS1, GSr1, and GSr2, with the same molecular weight (39.2kDa), but different pI values. GSI appeared at leaf emergence and was active throughout the leaf lifespan. GSII and GSIII, both located in the chloroplast, were each composed of a single 42.1kDa subunit with different pI values. GSII was active mainly in green leaves, while GSIII showed brief but higher activity in green leaves grown under field conditions. LC-MS/MS experiments revealed that GSII and GSIII have the same amino acid sequence, but GSII has more modification sites. With a modified blue native electrophoresis (BNE) technique and in-gel catalytic activity analysis, only two GS isoforms were observed: one cytosolic and one chloroplastic. Mass calibrations on BNE gels showed that the cytosolic GS1 holoenzyme was ~490kDa and likely a dodecamer, and the chloroplastic GS2 holoenzyme was ~240kDa and likely a hexamer. Lastly, our experimental data suggest that the activity of GS isoforms in wheat is regulated by subcellular localization, assembly, and modification to achieve their roles during plant development.},
doi = {10.1093/jxb/erv388},
journal = {Journal of Experimental Botany},
number = 21,
volume = 66,
place = {United States},
year = {Mon Aug 24 00:00:00 EDT 2015},
month = {Mon Aug 24 00:00:00 EDT 2015}
}

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Works referenced in this record:

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