Aspergillus oryzae NRRL 35191 from coffee, a non-toxigenic endophyte with the ability to synthesize kojic acid

2011 ◽  
Vol 11 (1) ◽  
pp. 263-267 ◽  
Author(s):  
Fabio C. Chaves ◽  
Thomas J. Gianfagna ◽  
Madhu Aneja ◽  
Francisco Posada ◽  
Stephen W. Peterson ◽  
...  
Author(s):  
Yuzhen Li ◽  
Huanxin Zhang ◽  
Ziming Chen ◽  
Junxia Fan ◽  
Tianming Chen ◽  
...  

2001 ◽  
Vol 91 (3) ◽  
pp. 272-276 ◽  
Author(s):  
Takafumi Futamura ◽  
Mitsuyasu Okabe ◽  
Takayoshi Tamura ◽  
Kyouko Toda ◽  
Toshio Matsunobu ◽  
...  

2013 ◽  
Vol 37 (6) ◽  
pp. 1095-1103 ◽  
Author(s):  
Shoubao Yan ◽  
Huijuan Tang ◽  
Shunchang Wang ◽  
Liangting Xu ◽  
Hongyan Liu ◽  
...  

2011 ◽  
Vol 75 (9) ◽  
pp. 1832-1834 ◽  
Author(s):  
Ken ODA ◽  
Akiko KOBAYASHI ◽  
Shinichi OHASHI ◽  
Motoaki SANO

2021 ◽  
Vol 2 ◽  
Author(s):  
Trong T. Dao ◽  
Kate M. J. de Mattos-Shipley ◽  
Ian M. Prosser ◽  
Katherine Williams ◽  
Marija K. Zacharova ◽  
...  

The use of filamentous fungi as cellular factories, where natural product pathways can be refactored and expressed in a host strain, continues to aid the field of natural product discovery. Much work has been done to develop host strains which are genetically tractable, and for which there are multiple selectable markers and controllable expression systems. To fully exploit these strains, it is beneficial to understand their natural metabolic capabilities, as such knowledge can rule out host metabolites from analysis of transgenic lines and highlight any potential interplay between endogenous and exogenous pathways. Additionally, once identified, the deletion of secondary metabolite pathways from host strains can simplify the detection and purification of heterologous compounds. To this end, secondary metabolite production in Aspergillus oryzae strain NSAR1 has been investigated via the deletion of the newly discovered negative regulator of secondary metabolism, mcrA (multicluster regulator A). In all ascomycetes previously studied mcrA deletion led to an increase in secondary metabolite production. Surprisingly, the only detectable phenotypic change in NSAR1 was a doubling in the yields of kojic acid, with no novel secondary metabolites produced. This supports the previous claim that secondary metabolite production has been repressed in A. oryzae and demonstrates that such repression is not McrA-mediated. Strain NSAR1 was then modified by employing CRISPR-Cas9 technology to disrupt the production of kojic acid, generating the novel strain NSARΔK, which combines the various beneficial traits of NSAR1 with a uniquely clean secondary metabolite background.


2019 ◽  
Vol 42 (5) ◽  
pp. 753-761 ◽  
Author(s):  
Weimeng Feng ◽  
Jinrui Liang ◽  
Bingbing Wang ◽  
Jianhua Chen

1998 ◽  
Vol 85 (5) ◽  
pp. 488-494 ◽  
Author(s):  
Yasushi Wakisaka ◽  
Takayuki Segawa ◽  
Koreyoshi Imamura ◽  
Takaharu Sakiyama ◽  
Kazuhiro Nakanishi

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