scholarly article | Q13442814 |
P2093 | author name string | Thomas A Bobik | |
Edith M Sampson | |||
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Protein content of polyhedral organelles involved in coenzyme B12-dependent degradation of 1,2-propanediol in Salmonella enterica serovar Typhimurium LT2 | Q31154125 | ||
The propanediol utilization (pdu) operon of Salmonella enterica serovar Typhimurium LT2 includes genes necessary for formation of polyhedral organelles involved in coenzyme B(12)-dependent 1, 2-propanediol degradation | Q33635809 | ||
Coordinate intracellular expression of Salmonella genes induced during infection. | Q33991109 | ||
Propionyl Coenzyme A Is a Common Intermediate in the 1,2-Propanediol and Propionate Catabolic Pathways Needed for Expression of the prpBCDE Operon during Growth of Salmonella enterica on 1,2-Propanediol | Q34191180 | ||
Cobalamin-dependent 1,2-propanediol utilization by Salmonella typhimurium | Q34191532 | ||
A single regulatory gene integrates control of vitamin B12 synthesis and propanediol degradation | Q34234308 | ||
PduP is a coenzyme-a-acylating propionaldehyde dehydrogenase associated with the polyhedral bodies involved in B 12 -dependent 1,2-propanediol degradation by Salmonella enterica serovar Typhimurium LT2 | Q34264452 | ||
PduA is a shell protein of polyhedral organelles involved in coenzyme B(12)-dependent degradation of 1,2-propanediol in Salmonella enterica serovar typhimurium LT2. | Q34305977 | ||
Cell-to-cell signalling in Escherichia coli and Salmonella enterica. | Q34319096 | ||
Ethanolamine utilization in Salmonella typhimurium: nucleotide sequence, protein expression, and mutational analysis of the cchA cchB eutE eutJ eutG eutH gene cluster | Q34319376 | ||
The control region of the pdu/cob regulon in Salmonella typhimurium | Q34332777 | ||
Minimal functions and physiological conditions required for growth of salmonella enterica on ethanolamine in the absence of the metabolosome | Q34468129 | ||
PduL is an evolutionarily distinct phosphotransacylase involved in B12-dependent 1,2-propanediol degradation by Salmonella enterica serovar typhimurium LT2. | Q34589424 | ||
Glutathione is required for maximal transcription of the cobalamin biosynthetic and 1,2-propanediol utilization (cob/pdu) regulon and for the catabolism of ethanolamine, 1,2-propanediol, and propionate in Salmonella typhimurium LT2. | Q35595241 | ||
DNA polymerase I function is required for the utilization of ethanolamine, 1,2-propanediol, and propionate by Salmonella typhimurium LT2 | Q35599859 | ||
The poc locus is required for 1,2-propanediol-dependent transcription of the cobalamin biosynthetic (cob) and propanediol utilization (pdu) genes of Salmonella typhimurium | Q36110570 | ||
Self-assembly in the carboxysome: a viral capsid-like protein shell in bacterial cells. | Q36825995 | ||
Studies of regulation of expression of the propionate (prpBCDE) operon provide insights into how Salmonella typhimurium LT2 integrates its 1,2-propanediol and propionate catabolic pathways | Q39568964 | ||
Anaerobic metabolism of the L-rhamnose fermentation product 1,2-propanediol in Salmonella typhimurium | Q39953118 | ||
Fermentation of 1,2-Propanediol and 1,2-Ethanediol by Some Genera of Enterobacteriaceae , Involving Coenzyme B 12 -Dependent Diol Dehydratase | Q39973227 | ||
Characterization of the propionyl-CoA synthetase (PrpE) enzyme of Salmonella enterica: residue Lys592 is required for propionyl-AMP synthesis | Q43883504 | ||
Biochemical evidence that the pduS gene encodes a bifunctional cobalamin reductase | Q46427803 | ||
A method for detection of phage mutants with altered transducing ability | Q50239404 | ||
Procedure for Identifying Nonsense Mutations | Q95780700 | ||
P433 | issue | 8 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 2966-71 | |
P577 | publication date | 2008-04-01 | |
P1433 | published in | Journal of Bacteriology | Q478419 |
P1476 | title | Microcompartments for B12-dependent 1,2-propanediol degradation provide protection from DNA and cellular damage by a reactive metabolic intermediate | |
P478 | volume | 190 |
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