Keiji Endo
Overview
Explore the profile of Keiji Endo including associated specialties, affiliations and a list of published articles.
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Articles
14
Citations
222
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0
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Recent Articles
1.
Fujimatsu T, Tsuno Y, Oonishi A, Yano T, Maeda H, Endo K, et al.
J Agric Food Chem
. 2024 Aug;
72(33):18465-18477.
PMID: 39110140
Legume plants form symbiotic relationships with rhizobia, which allow plants to utilize atmospheric nitrogen as a nutrient. This symbiosis is initiated by secretion of specific signaling metabolites from the roots,...
2.
Hioki T, Yamashita D, Tohata M, Endo K, Kawahara A, Okuda M
Microb Cell Fact
. 2021 Dec;
20(1):231.
PMID: 34963446
Background: Most of the proteases classified into the M23 family in the MEROPS database exhibit staphylolytic activity and have potential as antibacterial agents. The M23 family is further classified into...
3.
Fujimatsu T, Endo K, Yazaki K, Sugiyama A
Plant Direct
. 2020 Sep;
4(9):e00259.
PMID: 32995699
Soyasaponins are triterpenoid saponins widely found in legume plants. These compounds have drawn considerable attention because they have various activities beneficial for human health, and their biosynthesis has been actively...
4.
Tsuno Y, Fujimatsu T, Endo K, Sugiyama A, Yazaki K
Plant Cell Physiol
. 2017 Dec;
59(2):366-375.
PMID: 29216402
Root exudates are plant metabolites secreted from the roots into the soil. These exudates are involved in many important biological processes, including acquisition of nutrients, defense and signaling to rhizosphere...
5.
Shimojima M, Madoka Y, Fujiwara R, Murakawa M, Yoshitake Y, Ikeda K, et al.
Front Plant Sci
. 2015 Sep;
6:664.
PMID: 26379690
Inorganic phosphate (Pi) depletion is a serious problem for plant growth. Membrane lipid remodeling is a defense mechanism that plants use to survive Pi-depleted conditions. During Pi starvation, phospholipids are...
6.
Manabe K, Kageyama Y, Morimoto T, Ozawa T, Sawada K, Endo K, et al.
Appl Environ Microbiol
. 2011 Oct;
77(23):8370-81.
PMID: 21965396
Genome reduction strategies to create genetically improved cellular biosynthesis machineries for proteins and other products have been pursued by use of a wide range of bacteria. We reported previously that...
7.
Kakeshita H, Kageyama Y, Endo K, Tohata M, Ara K, Ozaki K, et al.
Biotechnol Lett
. 2011 May;
33(9):1847-52.
PMID: 21544609
Human interferon-β (hIFN-β) was used as a heterologous model protein to investigate the effects of the Bacillus subtilis AmyE propeptide and co-expression of PrsA in enhancing the secretion of heterologous...
8.
Liu S, Endo K, Ara K, Ozaki K, Ogasawara N
Microbiology (Reading)
. 2008 Sep;
154(Pt 9):2562-2570.
PMID: 18757790
We have developed a system for the induction of marker-free mutation of Bacillus subtilis. The system features both the advantages of the use of antibiotic-resistance markers for mutant selection, and...
9.
Morimoto T, Kadoya R, Endo K, Tohata M, Sawada K, Liu S, et al.
DNA Res
. 2008 Mar;
15(2):73-81.
PMID: 18334513
The emerging field of synthetic genomics is expected to facilitate the generation of microorganisms with the potential to achieve a sustainable society. One approach towards this goal is the reduction...
10.
Kodama T, Endo K, Sawada K, Ara K, Ozaki K, Kakeshita H, et al.
J Biosci Bioeng
. 2007 Sep;
104(2):135-43.
PMID: 17884659
In Bacillus subtilis, extracellular protease-deficient mutants have been used in attempts to increase the productivity of heterologous proteins. We detected protease activity of AprX using protease zymography in the culture...