Distribution of storage proteins in low-glutelin rice seed determined using a fluorescent antibody

2003 ◽  
Vol 96 (5) ◽  
pp. 467-473 ◽  
Author(s):  
Sachiko Furukawa ◽  
Tomochika Mizuma ◽  
Yoshifumi Kiyokawa ◽  
Takehiro Masumura ◽  
Kunisuke Tanaka ◽  
...  
1999 ◽  
Vol 16 (2) ◽  
pp. 103-113 ◽  
Author(s):  
Norihiro MITSUKAWA ◽  
Ryoichi KONISHI ◽  
Kunitomo KIDZU ◽  
Kozo OHTSUKI ◽  
Takehiro MASUMURA ◽  
...  

2010 ◽  
Vol 19 (1) ◽  
pp. 123-126 ◽  
Author(s):  
Soma Marla ◽  
Deeksha Bharatiya ◽  
Madhu Bala ◽  
Vinay Singh ◽  
Anil Kumar

Plant Science ◽  
1990 ◽  
Vol 70 (1) ◽  
pp. 73-80 ◽  
Author(s):  
Y.R. Mawal ◽  
M.R. Mawal ◽  
M.N. Sainani ◽  
P.K. Ranjekar

2021 ◽  
Author(s):  
Jianping Zhu ◽  
Yulong Ren ◽  
Yuanyan Zhang ◽  
Jie Yang ◽  
Erchao Duan ◽  
...  

AbstractDense vesicles (DVs) are Golgi-derived plant-specific carriers that mediate post-Golgi transport of seed storage proteins in angiosperms. How this process is regulated remains elusive. Here, we report a rice (Oryza sativa) mutant, named glutelin precursor accumulation8 (gpa8) that abnormally accumulates 57-kDa proglutelins in the mature endosperm. Cytological analyses of the gpa8 mutant revealed that proglutelin-containing DVs were mistargeted to the apoplast forming electron-dense aggregates and paramural bodies in developing endosperm cells. Differing from previously reported gpa mutants with post-Golgi trafficking defects, the gpa8 mutant showed bent Golgi bodies, defective trans-Golgi network (TGN), and enlarged DVs, suggesting a specific role of GPA8 in DV biogenesis. We demonstrated that GPA8 encodes a subunit E isoform 1 of vacuolar H+-ATPase (OsVHA-E1) that mainly localizes to TGN and the tonoplast. Further analysis revealed that the luminal pH of the TGN and vacuole is dramatically increased in the gpa8 mutant. Moreover, the colocalization of GPA1 and GPA3 with TGN marker protein in gpa8 protoplasts was obviously decreased. Our data indicated that OsVHA-E1 is involved in endomembrane luminal pH homeostasis, as well as maintenance of Golgi morphology and TGN required for DV biogenesis and subsequent protein trafficking in rice endosperm cells.


2021 ◽  
Vol 12 ◽  
Author(s):  
Ai Sasou ◽  
Yoshikazu Yuki ◽  
Shiho Kurokawa ◽  
Shintaro Sato ◽  
Yuki Goda ◽  
...  

Human norovirus is the leading cause of acute nonbacterial gastroenteritis in people of all ages worldwide. Currently, no licensed norovirus vaccine, pharmaceutical drug, or therapy is available for the control of norovirus infection. Here, we used a rice transgenic system, MucoRice, to produce a variable domain of a llama heavy-chain antibody fragment (VHH) specific for human norovirus (MucoRice-VHH). VHH is a small heat- and acid-stable protein that resembles a monoclonal antibody. Consequently, VHHs have become attractive and useful antibodies (Abs) for oral immunotherapy against intestinal infectious diseases. MucoRice-VHH constructs were generated at high yields in rice seeds by using an overexpression system with RNA interference to suppress the production of the major rice endogenous storage proteins. The average production levels of monomeric VHH (7C6) to GII.4 norovirus and heterodimeric VHH (7C6-1E4) to GII.4 and GII.17 noroviruses in rice seed were 0.54 and 0.28% (w/w), respectively, as phosphate buffered saline (PBS)-soluble VHHs. By using a human norovirus propagation system in human induced pluripotent stem-cell-derived intestinal epithelial cells (IECs), we demonstrated the high neutralizing activity of MucoRice expressing monomeric VHH (7C6) against GII.4 norovirus and of heterodimeric VHH (7C6-1E4) against both GII.4 and GII.17 noroviruses. In addition, MucoRice-VHH (7C6-1E4) retained neutralizing activity even after heat treatment at 90°C for 20 min. These results build a fundamental platform for the continued development of MucoRice-VHH heterodimer as a candidate for oral immunotherapy and for prophylaxis against GII.4 and GII.17 noroviruses in not only healthy adults and children but also immunocompromised patients and the elderly.


Nature ◽  
2000 ◽  
Vol 407 (6805) ◽  
pp. 765-767 ◽  
Author(s):  
Sang-Bong Choi ◽  
Changlin Wang ◽  
Douglas G. Muench ◽  
Kenjirou Ozawa ◽  
Vincent R. Franceschi ◽  
...  

Plant Science ◽  
2021 ◽  
pp. 111049
Author(s):  
Hiroaki Matsusaka ◽  
Masako Fukuda ◽  
Ammar Elakhdar ◽  
Toshihiro Kumamaru

2011 ◽  
Vol 38 (4) ◽  
pp. 263-271 ◽  
Author(s):  
Young-Mi Kim ◽  
Jong-Yeol Lee ◽  
Ung-Han Yoon ◽  
Sang-Bong Choi ◽  
Sun-Hwa Ha ◽  
...  

Author(s):  
Kenjiro Yasuda

Localization of amylase,chymotrypsinogen and trypsinogen in pancreas was demonstrated by Yasuda and Coons (1966), by using fluorescent antibody method. These enzymes were naturally found in the zymogen granules. Among them, amylase showed a diffuse localization around the nucleus, in addition to the zymogen granules. Using ferritin antibody method, scattered ferritin granules were also found around the Golgi area (Yasuda et al.,1967). The recent advance in the tissue preparation enables the antigen to be localized in the ultrathin frozen sections, by applying the labeled antibodies onto the sections instead of staining the tissue en bloc.The present study deals with the comparison of the localization of amylase and lipase demonstrated by applying the bismuth-labeled, peroxidase-labeled and ferritin-labeled antibody methods on the ultrathin frozen sections of pancreas, and on the blocks of the same tissue.


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