scholarly journals In Vivo Screening for Biocontrol Agents (BCAs) against Streptomyces scabiei Causing Potato Common Scab

2004 ◽  
Vol 20 (2) ◽  
pp. 110-114 ◽  
Author(s):  
Hyang-Burm Lee ◽  
Jong-Wun Cho ◽  
Dong-Jin Park ◽  
Chang-Tian Li ◽  
Young-Hwan Ko ◽  
...  
2007 ◽  
Vol 32 (2) ◽  
pp. 131-134
Author(s):  
Masahiro Natsume ◽  
Atsushi Ooshiro ◽  
Tsuneki Takahashi ◽  
Fumihiko Kokido ◽  
Makoto Hashimoto ◽  
...  

ACS Omega ◽  
2021 ◽  
Vol 6 (17) ◽  
pp. 11474-11487
Author(s):  
Jingyu Liu ◽  
Louis-Félix Nothias ◽  
Pieter C. Dorrestein ◽  
Kapil Tahlan ◽  
Dawn R. D. Bignell

2011 ◽  
Vol 24 (5) ◽  
pp. 622-627 ◽  
Author(s):  
Jong-In Park ◽  
Hee-Jeong Jung ◽  
Yong-Hui Bae ◽  
Kwon-Kyoo Kang ◽  
Ill-Sup Nou

2015 ◽  
Vol 30 (3) ◽  
pp. 245-253 ◽  
Author(s):  
Rebeca Padilla-Reynaud ◽  
Anne-Marie Simao-Beaunoir ◽  
Sylvain Lerat ◽  
Mark A. Bernards ◽  
Carole Beaulieu

2017 ◽  
Vol 40 (1) ◽  
pp. 70-75 ◽  
Author(s):  
Maxime C. Paré ◽  
Jean Legault ◽  
André Pichette ◽  
Catherine Tremblay ◽  
Marie-France Aubut

2016 ◽  
Vol 4 (2) ◽  
Author(s):  
Tsuyoshi Tomihama ◽  
Yatsuka Nishi ◽  
Masao Sakai ◽  
Makoto Ikenaga ◽  
Takashi Okubo ◽  
...  

The draft genome sequences of the three pathogens of potato common scab, Streptomyces scabiei S58, Streptomyces turgidiscabies T45, and Streptomyces acidiscabies a10, isolated in Japan, are presented here. The genome size of each strain is >10 Mb, and the three pathogenic strains share genes located in a pathogenicity island previously described in other pathogenic Streptomyces species.


2019 ◽  
Vol 15 (1) ◽  
pp. 63-70
Author(s):  
Shiv Dev Singh ◽  
Arvind Kumar ◽  
Firoz Babar ◽  
Neetu Sachan ◽  
Arun Kumar Sharma

Background: Thienopyrimidines are the bioisoster of quinazoline and unlike quinazoline exist in three isomeric forms corresponding to the three possible types annulation of thiophene to the pyrimidine ring viz thieno[2,3-d] pyrimidine, thieno[3,2-d] pyrimidine and thieno[3,4-d]pyrimidine. Heterocyclic containing the thienopyrimidinone moiety exhibits various pronounced activities such as anti-hypertensive, analgesic and anti-inflammatory, antiviral, platelet aggregation inhibitory, antiprotozoal bronchodilatory, phosphodiesterase inhibitory, antihistaminic, antipsychotic and antimicrobial activity. Objective: Synthesis of novel 3(N,N-dialkylamino)alkyl/phenyl substituted thieno[2,3-d]pyrimidinones as H1-anti-histaminic and antimicrobial agents. Methods: A series of 3-[(N,N-dialkylamino)alkyl/phenyl]-2-(1H)thioxo-5,6,7,8-tetrahydrobenzo(b) thieno(2,3-d)pyrimidine-4(3H)-ones[4a-d], their oxo analogous [5a-d] and 3-[(N,N-dialkylamino)alkyl]- 2-chlorophenyl-5,6,7,8-tetrahydrobenzo(b)thieno(2,3-d)pyrimidine- 4 (3H)-ones[6a-d]derivative were synthesized from 2-amino-4,5,6,7-tetrahydrobenzo(b)thiophene-3-carboxylic acid by nucleophilic substitution of different N,N-dialkyl alkylene/phenylene diamines on activated 3-acylchloride moiety followed by cyclocondensation with carbon disulfide and ethanolic potassium hydroxide to get [4a-d] and in second reaction by condensation with 4-chlorobenzoyl chloride to get [6a-d] by single pot novel innovative route. The oxo analogous [5a-d] were prepared by treating derivatives [4a-d] with potassium permagnate in ethanolic KOH. The synthesized compound were evaluated for H1-antihistaminic and antimicrobial activities. Results: All synthesized compounds exhibited significant H1-antihistaminic activity by in vitro and in vivo screening methods and data were verified analytically and statistically. The compound 4a, 4b, 5a and 5b showed significant H1-antihistaminiic activity than the reference standard chlorpheniramine maleate. The compound 6d, 6c, 5c and 4c exhibited significant antimicrobial activity.


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