Acetate metabolism in Penicillium griseofulvum

1965 ◽  
Vol 112 (1) ◽  
pp. 163-169 ◽  
Author(s):  
Robley J. Light
Author(s):  
Ekaterina Krumova ◽  
Radoslav Abrashev ◽  
Vladislava Dishliyska ◽  
Galina Stoyancheva ◽  
Nedelina Kostadinova ◽  
...  

2021 ◽  
Vol 186 ◽  
pp. 112708
Author(s):  
Yi Zang ◽  
Yihua Gong ◽  
Xia Chen ◽  
Huiling Wen ◽  
Changxing Qi ◽  
...  

1959 ◽  
Vol 234 (2) ◽  
pp. 435-437 ◽  
Author(s):  
R.J. Emerson ◽  
W.C. Bernards ◽  
J.T. Van Bruggen

2013 ◽  
Vol 132 ◽  
pp. 178-181 ◽  
Author(s):  
Yin Chen ◽  
Wenjun Mao ◽  
Baofeng Wang ◽  
Lina Zhou ◽  
Qianqun Gu ◽  
...  

2014 ◽  
Vol 80 (15) ◽  
pp. 4599-4605 ◽  
Author(s):  
Amelia-Elena Rotaru ◽  
Pravin Malla Shrestha ◽  
Fanghua Liu ◽  
Beatrice Markovaite ◽  
Shanshan Chen ◽  
...  

ABSTRACTDirect interspecies electron transfer (DIET) is potentially an effective form of syntrophy in methanogenic communities, but little is known about the diversity of methanogens capable of DIET. The ability ofMethanosarcina barkerito participate in DIET was evaluated in coculture withGeobacter metallireducens. Cocultures formed aggregates that shared electrons via DIET during the stoichiometric conversion of ethanol to methane. Cocultures could not be initiated with a pilin-deficientG. metallireducensstrain, suggesting that long-range electron transfer along pili was important for DIET. Amendments of granular activated carbon permitted the pilin-deficientG. metallireducensisolates to share electrons withM. barkeri, demonstrating that this conductive material could substitute for pili in promoting DIET. WhenM. barkeriwas grown in coculture with the H2-producingPelobacter carbinolicus, incapable of DIET,M. barkeriutilized H2as an electron donor but metabolized little of the acetate thatP. carbinolicusproduced. This suggested that H2, but not electrons derived from DIET, inhibited acetate metabolism.P. carbinolicus-M. barkericocultures did not aggregate, demonstrating that, unlike DIET, close physical contact was not necessary for interspecies H2transfer.M. barkeriis the second methanogen found to accept electrons via DIET and the first methanogen known to be capable of using either H2or electrons derived from DIET for CO2reduction. Furthermore,M. barkeriis genetically tractable, making it a model organism for elucidating mechanisms by which methanogens make biological electrical connections with other cells.


2004 ◽  
Vol 186 (9) ◽  
pp. 2798-2809 ◽  
Author(s):  
Robert Gerstmeir ◽  
Annette Cramer ◽  
Petra Dangel ◽  
Steffen Schaffer ◽  
Bernhard J. Eikmanns

ABSTRACT The adaptation of Corynebacterium glutamicum to acetate as a carbon and energy source involves transcriptional regulation of the pta-ack operon coding for the acetate-activating enzymes phosphotransacetylase and acetate kinase and of the aceA and aceB genes coding for the glyoxylate cycle enzymes isocitrate lyase and malate synthase, respectively. Deletion and mutation analysis of the respective promoter regions led to the identification of highly conserved 13-bp motifs (AA/GAACTTTGCAAA) as cis-regulatory elements for expression of the pta-ack operon and the aceA and aceB genes. By use of DNA affinity chromatography, a 53-kDa protein specifically binding to the promoter/operator region of the pta-ack operon was purified. Mass spectrometry and peptide mass fingerprinting identified the protein as a putative transcriptional regulator (which was designated RamB). Purified His-tagged RamB protein was shown to bind specifically to both the pta-ack and the aceA/aceB promoter/operator regions. Directed deletion of the ramB gene in the genome of C. glutamicum resulted in mutant strain RG1. Whereas the wild type of C. glutamicum showed high-level specific activities of acetate kinase, phosphotransacetylase, isocitrate lyase, and malate synthase when grown on acetate and low-level specific activities when grown on glucose as sole carbon and energy sources, mutant RG1 showed high-level specific activities with all four enzymes irrespective of the substrate. Comparative transcriptional cat fusion experiments revealed that this deregulation takes place at the level of transcription. The results indicate that RamB is a negative transcriptional regulator of genes involved in acetate metabolism of C. glutamicum.


1967 ◽  
Vol 190 (2) ◽  
pp. 295-307 ◽  
Author(s):  
D. Pauline Alexander ◽  
H. G. Britton ◽  
D. A. Nixon
Keyword(s):  

1983 ◽  
Vol 80 (19) ◽  
pp. 5847-5851 ◽  
Author(s):  
J. R. Dickinson ◽  
I. W. Dawes ◽  
A. S. Boyd ◽  
R. L. Baxter

2017 ◽  
Vol 19 (suppl_6) ◽  
pp. vi131-vi131
Author(s):  
Chloe Najac ◽  
Marina Radoul ◽  
Pavithra Viswanath ◽  
Myriam M Chaumeil ◽  
Sabrina Ronen

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