Optical and Physiological Properties of a Plant Canopy

2016 ◽  
pp. 125-135 ◽  
Author(s):  
Yasuomi Ibaraki
2019 ◽  
Vol 57 (6) ◽  
pp. 665 ◽  
Author(s):  
Yen Thi Hoang ◽  
Quynh Thi Thu Tran ◽  
Ha Hoang Chu ◽  
Tuyen Thi Do ◽  
Thanh Tat Dang ◽  
...  

Purple nonsulfur bacteria are a group that has so much biotechnological applications, particularly in producing of functional food rich with unsaturated fatty acids. A purple nonsulfur bacterium (named HPB.6) was chosen based on its strong growth, high lipid and synthesis of unsaturated fatty acid (omega 6,7,9). Studying on basic biological characteristics showed that the cells of HPB.6 were observed as ovoid-rod shape, none motility, Gram negative staining. The diameter of single bacterium was about 0.8-1.0 µm. The cells divide by binary fission and had bacteriochlorophyll a (Bchl a). This bacterium grew well on medium with carbon and nitrogen sources such as acetate, succinate, pyruvate, butyrate, glutamate, arginine, leucine, tyrosine, alanine, methionine, threonine, glutamine, yeast extract and NH4Cl. This selected strain grew well on medium with salt concentrations from 1.5 - 6.0% (optimum 3%), pH from 5.0 to 8.0 (optimum at pH 6.5) and could withstand Na2S at 4.0 - 5.2 mM. Based on morphological, physiological properties and 16S rRNA analysis received demonstrated that HPB.6 strain belongs to the species Rhodovulum sulfidophilum.


2019 ◽  
Author(s):  
Michael Oschmann ◽  
Linus Johansson Holm ◽  
Oscar Verho

Benzofurans are everywhere in nature and they have been extensively studied by medicinal chemists over the years because of their chemotherapeutic and physiological properties. Herein, we describe a strategy that can be used to access elaborate benzo-2-carboxamide derivatives, which involves a synthetic sequence of 8-aminoquinoline directed C–H arylations followed by transamidations. For the directed C–H arylations, Pd catalysis was used to install a wide range of aryl and heteroaryl substituents at the C3 position of the benzofuran scaffold in high efficiency. Directing group cleavage and further diversification of the C3-arylated benzofuran products were then achieved in a single synthetic operation through the utilization of a two-step transamidation protocol. By bocylating the 8-aminoquinoline amide moiety of these products, it proved possible to activate them towards aminolysis with different amine nucleophiles. Interestingly, this aminolysis reaction was found to proceed efficiently without the need of any additional catalyst or additive. Given the high efficiency and modularity of this synthetic strategy, it constitute a very attractive approach for generating structurally-diverse collections of benzofuran derivatives for small molecule screening.


2019 ◽  
Vol 10 (7) ◽  
pp. 1460-1465
Author(s):  
Prabhakar Mishra ◽  
Manish Upadhayay ◽  
G. P. Khare ◽  
D.S. Thakur

2010 ◽  
Vol 26 (4) ◽  
pp. 533-542 ◽  
Author(s):  
Tuerhong Tuerxun· ◽  
Abuduwaili Jilili· ◽  
Yilahong Aikebaier· ◽  
Dong-wei LIU

2009 ◽  
Vol 38 (12) ◽  
pp. 1656-1663 ◽  
Author(s):  
Joon-Ho Hwang ◽  
You-Sung Oh ◽  
Ja-Hun Lim ◽  
Ji-Eun Park ◽  
Mi-Bo Kim ◽  
...  

HortScience ◽  
1998 ◽  
Vol 33 (3) ◽  
pp. 447f-448
Author(s):  
Millie S. Williams ◽  
Terri Woods Starman ◽  
James E. Faust

Flower growers experience decreased consumer satisfaction with plant species that cease flowering during the summer. The objective of this experiment was to characterize the heat tolerance of four specialty floral crop species in order to predict their summer performance in the different climatalogical regions of the United States. The effect of increasing temperatures on the duration of postharvest flower development was determined for Ageranthemum frutescens `Butterfly' and `Sugar Baby', Brachycome hybrid `Ultra', and Sutera cordata `Snowflake'. Plants were grown in a 18 °C greenhouse until marketable with foliage covering the container and flowers distributed evenly across the plant canopy. Plants were then placed in a phytotron to determine their heat tolerance. Temperature set points of 18, 23, 28, and 33 °C were delivered serially at 2-week intervals, starting at 18 °C. Plants were then returned to 18 °C after the 33 °C treatment. Immature flower bud, mature flower bud, flower and senesced flower numbers were collected once per week. Sutera `Snowflake', and Brachycome `Ultra' had the greatest flower number at the 23 °C temperature, decreasing in the 28 °C environment. Argeranthemum `Butterfly' and `Sugar Baby' had greatest flower number at 28 °C, but flowers were smaller and of lower quality than at 23 °C. Flower development of all cultivars ceased at 33 °C, but when plants were returned to the 18 °C production greenhouse, flower development resumed. According to normal average daily temperatures in Knoxville, Tenn., Ageranthemum frutescens `Butterfly' and `Sugar Baby' would flower until mid-June, while Brachycome hybrid `Ultra' and Sutera cordata `Snowflake' would flower until mid-May.


2019 ◽  
Vol 22 (8) ◽  
pp. 570-576
Author(s):  
Maryam Shokrollahi ◽  
Marjaneh Samadizadeh ◽  
Mohsen Khalili ◽  
Seyed A. Sobhanian ◽  
Abbas Ahmadi

Background: Phencyclidine (PCP, I) is a synthetic drug with remarkable physiological properties. PCP and its analogues exert many pharmacological activities and interact with some neurotransmitter systems in the central nervous system like particular affinity for PCP sites in NMDA receptors or dopamine uptake blocking or even both. Aim and Objective: The following research, methyl group with electron-donating and dipole moment characters was added in different positions of phenyl ring along with the substitution of benzylamine (with many pharmacological effects) instead of piperidine ring of I to produce new compounds (II-V) of this family with more analgesic activities. Materials and Methods: Analgesic activities of these new compounds were measured by tail immersion and formalin tests for acute and chronic pains, respectively. Also, the outcomes were compared with control and PCP (10 mg/kg) groups. Results: The results indicate that compounds III, IV, and V have more acute and chronic antinociceptive effects than PCP and compound II which may be concerned with more antagonizing activities of these new painkillers for the blockage of dopamine reuptake as well as high affinity for NMDA receptors PCP binding site. Conclusion: It can be concluded that the benzylamine derivative of phencyclidine with a methyl group on the benzyl position on phenyl ring (V) is a more appropriate candidate to reduce acute and chronic (thermal and chemical) pains compared to other substituted phenyl analogs (II-IV) and PCP.


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