scholarly journals Simultaneously down-regulation of multiplex branch pathways using CRISPRi and fermentation optimization for enhancing β-amyrin production in Saccharomyces cerevisiae

2019 ◽  
Vol 4 (2) ◽  
pp. 79-85 ◽  
Author(s):  
Jiangping Ni ◽  
Genlin Zhang ◽  
Lei Qin ◽  
Jun Li ◽  
Chun Li
2021 ◽  
Vol 14 (1) ◽  
Author(s):  
Marlous van Dijk ◽  
Peter Rugbjerg ◽  
Yvonne Nygård ◽  
Lisbeth Olsson

Abstract Background The limited tolerance of Saccharomyces cerevisiae to inhibitors is a major challenge in second-generation bioethanol production, and our understanding of the molecular mechanisms providing tolerance to inhibitor-rich lignocellulosic hydrolysates is incomplete. Short-term adaptation of the yeast in the presence of dilute hydrolysate can improve its robustness and productivity during subsequent fermentation. Results We utilized RNA sequencing to investigate differential gene expression in the industrial yeast strain CR01 during short-term adaptation, mimicking industrial conditions for cell propagation. In this first transcriptomic study of short-term adaption of S. cerevisiae to lignocellulosic hydrolysate, we found that cultures respond by fine-tuned up- and down-regulation of a subset of general stress response genes. Furthermore, time-resolved RNA sequencing allowed for identification of genes that were differentially expressed at 2 or more sampling points, revealing the importance of oxidative stress response, thiamin and biotin biosynthesis. furan-aldehyde reductases and specific drug:H+ antiporters, as well as the down-regulation of certain transporter genes. Conclusions These findings provide a better understanding of the molecular mechanisms governing short-term adaptation of S. cerevisiae to lignocellulosic hydrolysate, and suggest new genetic targets for improving fermentation robustness.


2007 ◽  
Vol 43 (10) ◽  
pp. 1458-1465 ◽  
Author(s):  
A MATIAS ◽  
N PEDROSO ◽  
N TEODORO ◽  
H MARINHO ◽  
F ANTUNES ◽  
...  

1989 ◽  
Vol 9 (9) ◽  
pp. 3720-3726
Author(s):  
D Blinder ◽  
D D Jenness

alpha-Factor pheromone inhibits division of yeast a cells. After prolonged exposure to alpha-factor, the cells adapt to the stimulus and resume cell division. The sst2 mutation is known to inhibit adaptation. This report examines adaptation in scg1 (also designated gpa1) and STE4Hpl (Hpl indicates haploid lethal) mutants that exhibit constitutive activation of the pheromone response pathway. Recovery of the STE4Hpl mutant was blocked by the sst2-1 mutation, whereas recovery of the scg1-7 mutant was not completely blocked by sst2-1. These results indicate that both SST2-dependent and -independent mechanisms regulate postreceptor events in the pheromone response pathway. Down regulation of receptors in response to alpha-factor was independent of the signal that was generated in the scg1 mutant.


2004 ◽  
Vol 3 (4) ◽  
pp. 893-899 ◽  
Author(s):  
George K. Arhin ◽  
Shuiyuan Shen ◽  
Henriette Irmer ◽  
Elisabetta Ullu ◽  
Christian Tschudi

ABSTRACT tRNAs are transcribed as precursors containing 5′ leader and 3′ extensions that are removed by a series of posttranscriptional processing reactions to yield functional mature tRNAs. Here, we examined the maturation pathway of tRNAMet in Trypanosoma brucei, an early divergent unicellular eukaryote. We identified an approximately 300-kDa complex located in the nucleus of T. brucei that is required for trimming the 5′ leader of initiator tRNAMet precursors. One of the subunits of the complex (T. brucei MT40 [TbMT40]) is a putative methyltransferase and a homolog of Saccharomyces cerevisiae Gcd14, which is essential for 1-methyladenosine modification in tRNAs. Down-regulation of TbMT40 by RNA interference resulted in the accumulation of precursor initiator tRNAMet containing 5′ extensions but processed 3′ ends. In addition, immunoprecipitations with anti-La antibodies revealed initiator tRNAMet molecules with 5′ and 3′ extensions in TbMT40-silenced cells, albeit at a much lower level. Interestingly, silencing of TbMT40, as well as of TbMT53, a second subunit of the complex, led to an increase in the levels of mature elongator tRNAMet. Taken together, our data provide a glance at the maturation of tRNAs in parasitic protozoa and suggest that at least for initiator tRNAMet, 3′ trimming precedes 5′ processing.


PLoS ONE ◽  
2019 ◽  
Vol 14 (4) ◽  
pp. e0215870
Author(s):  
Catherine Tesnière ◽  
Chloé Bessière ◽  
Martine Pradal ◽  
Isabelle Sanchez ◽  
Bruno Blondin ◽  
...  

2015 ◽  
Vol 51 (7) ◽  
pp. 766-773 ◽  
Author(s):  
K. V. Sidoruk ◽  
L. I. Davydova ◽  
D. G. Kozlov ◽  
D. G. Gubaidullin ◽  
A. V. Glazunov ◽  
...  

1989 ◽  
Vol 9 (9) ◽  
pp. 3720-3726 ◽  
Author(s):  
D Blinder ◽  
D D Jenness

alpha-Factor pheromone inhibits division of yeast a cells. After prolonged exposure to alpha-factor, the cells adapt to the stimulus and resume cell division. The sst2 mutation is known to inhibit adaptation. This report examines adaptation in scg1 (also designated gpa1) and STE4Hpl (Hpl indicates haploid lethal) mutants that exhibit constitutive activation of the pheromone response pathway. Recovery of the STE4Hpl mutant was blocked by the sst2-1 mutation, whereas recovery of the scg1-7 mutant was not completely blocked by sst2-1. These results indicate that both SST2-dependent and -independent mechanisms regulate postreceptor events in the pheromone response pathway. Down regulation of receptors in response to alpha-factor was independent of the signal that was generated in the scg1 mutant.


2015 ◽  
Vol 472 (3) ◽  
pp. 319-328 ◽  
Author(s):  
Non Miyata ◽  
Takuya Miyoshi ◽  
Takanori Yamaguchi ◽  
Toshimitsu Nakazono ◽  
Motohiro Tani ◽  
...  

Regulation of expression of the PS decarboxylase 2 (PSD2) gene in Saccharomyces cerevisiae is poorly understood. We found that deletion of VID22 resulted in a decrease in the activity of the Psd2p enzyme through down-regulation of PSD2 gene expression.


Microbiology ◽  
1999 ◽  
Vol 145 (2) ◽  
pp. 309-316 ◽  
Author(s):  
Nianshu Zhang ◽  
David C. J. Gardner ◽  
Stephen G. Oliver ◽  
Lubomira I. Stateva

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