Amir Reza Jassbi

Prof. Amir Reza Jassbi

orcid

Research Focus & Metrics

Academic Career Length

30Years (1997-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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13 October 2015 in Critical Reviews in Food Science and Nutrition
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Journal Article
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Jianbo XiaoJianbo Xiao
Jianbo Xiao
Esra CapanogluEsra Capanoglu
Esra Capanoglu
AJAmir Reza Jassbi
Amir Reza Jassbi
AMAnca Miron
Anca Miron
The dietary flavonoids, especially their glycosides, are the most vital phytochemicals in diets and are of great general interest due to their diverse bioactivity. Almost all natural flavonoids exist as their O-glycoside or C-glycoside forms in plants. The dietary flavonoid C-glycosides have received less attention than their corresponding O-glycosides. This review summarizes current knowledge regarding flavonoid C-glycosides and their influence on human health. Among the flavonoid C-glycosides, flavone C-glycosides, especially vitexin, isoorientin, orientin, isovitexin and their multiglycosides are more frequently mentioned than others. Flavonoid C-monoglycosides are poorly absorbed in human beings with very few metabolites in urine and blood and are deglycosylated and degraded by human intestinal bacteria in colon. However, flavonoid C-multiglycosides are absorbed unchanged in the intestine and distributed to other tissues. Flavonoid C-glycosides showed significant antioxidant activity, anticancer and antitumor activity, hepatoprotective activity, anti-inflammatory activity, anti-diabetes activity, antiviral activity, antibacterial and antifungal activity, and other biological effects. It looks like that the C-glycosylflavonoids in most cases showed higher antioxidant and anti-diabetes potential than their corresponding O-glycosylflavonoids and aglycones. However, there is a lack of in vivo data on the biological benefits of flavonoid C-glycosides. It is necessary to investigate more on how flavonoid C-glycosides prevent and handle the diseases.

1 January 2015 in Biotechnology Advances
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Journal Article
Closed access
HCHui Cao
Hui Cao
XCXiaoqing Chen
Xiaoqing Chen
AJAmir Reza Jassbi
Amir Reza Jassbi
Jianbo XiaoJianbo Xiao
Jianbo Xiao

1 September 2006 in Phytochemistry
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Journal Article
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AJAmir Reza Jassbi
Amir Reza Jassbi

1 January 2010 in The Plant Cell
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Journal Article
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SHSven Heiling
Sven Heiling
MSMeredith Schuman
Meredith Schuman
MSMatthias Schoettner
Matthias Schoettner
PMPurba Mukerjee
Purba Mukerjee
BBBeatrice Berger
Beatrice Berger
IBIan T. Baldwin
Ian T. Baldwin
We identified 11 17-hydroxygeranyllinalool diterpene glycosides (HGL-DTGs) that occur in concentrations equivalent to starch (mg/g fresh mass) in aboveground tissues of coyote tobacco (Nicotiana attenuata) and differ in their sugar moieties and malonyl sugar esters (0-2). Concentrations of HGL-DTGs, particularly malonylated compounds, are highest in young and reproductive tissues. Within a tissue, herbivore elicitation changes concentrations and biosynthetic kinetics of individual compounds. Using stably transformed N. attenuata plants silenced in jasmonate production and perception, or production of N. attenuata Hyp-rich glycopeptide systemin precursor by RNA interference, we identified malonylation as the key biosynthetic step regulated by herbivory and jasmonate signaling. We stably silenced N. attenuata geranylgeranyl diphosphate synthase (ggpps) to reduce precursors for the HGL-DTG skeleton, resulting in reduced total HGL-DTGs and greater vulnerability to native herbivores in the field. Larvae of the specialist tobacco hornworm (Manduca sexta) grew up to 10 times as large on ggpps silenced plants, and silenced plants suffered significantly more damage from herbivores in N. attenuata9s native habitat than did wild-type plants. We propose that high concentrations of HGL-DTGs effectively defend valuable tissues against herbivores and that malonylation may play an important role in regulating the distribution and storage of HGL-DTGs in plants.

1 January 2021 in European Journal of Medicinal Chemistry
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Journal Article
Closed access
MGMohsen Gozari
Mohsen Gozari
MAMaryam Alborz
Maryam Alborz
HEHesham R. El-Seedi
Hesham R. El-Seedi
AJAmir Reza Jassbi
Amir Reza Jassbi

24 April 2021 in Marine Drugs
Verified
Journal Article
Open access
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SKShaden Khalifa
Shaden Khalifa
ESEslam Shedid
Eslam Shedid
Essa M. SaiedEssa M. Saied
Essa M. Saied
AJAmir Reza Jassbi
Amir Reza Jassbi
FJFatemeh H. Jamebozorgi
Fatemeh H. Jamebozorgi
Hesham El-SeediHesham El-Seedi
Hesham El-Seedi
Cyanobacteria are photosynthetic prokaryotic organisms which represent a significant source of novel, bioactive, secondary metabolites, and they are also considered an abundant source of bioactive compounds/drugs, such as dolastatin, cryptophycin 1, curacin toyocamycin, phytoalexin, cyanovirin-N and phycocyanin. Some of these compounds have displayed promising results in successful Phase I, II, III and IV clinical trials. Additionally, the cyanobacterial compounds applied to medical research have demonstrated an exciting future with great potential to be developed into new medicines. Most of these compounds have exhibited strong pharmacological activities, including neurotoxicity, cytotoxicity and antiviral activity against HCMV, HSV-1, HHV-6 and HIV-1, so these metabolites could be promising candidates for COVID-19 treatment. Therefore, the effective large-scale production of natural marine products through synthesis is important for resolving the existing issues associated with chemical isolation, including small yields, and may be necessary to better investigate their biological activities. Herein, we highlight the total synthesized and stereochemical determinations of the cyanobacterial bioactive compounds. Furthermore, this review primarily focuses on the biotechnological applications of cyanobacteria, including applications as cosmetics, food supplements, and the nanobiotechnological applications of cyanobacterial bioactive compounds in potential medicinal applications for various human diseases are discussed.