Cellvibrio japonicus Ueda107

Gram-negativeRodMotileAerobe

Kingdom

Pseudomonadati

Phylum

Pseudomonadota

Class

Gammaproteobacteria

Order

Cellvibrionales

Family

Cellvibrionaceae

Genus

Cellvibrio

Description

Cellvibrio japonicus (Strain Ueda107) is an aerobic Gram-negative saprophytic soil bacterium that was isolated from Japanese soil in 1952 and named Pseudomonas fluorescens subsp. cellulosa. Recent studies however demonstrated that C. japonicus is not a member of the genus Pseudomonas but is closely related to Cellvibrio mixtus, and hence the bacterium was renamed. C. japonicus represents an excellent system for studying the mechanism of plant cell wall degradation in a Gram-negative, non-cellulosomic saprophyte. It contains the complete repertoire of enzymes (glycoside hydrolases, lyases and esterases) required to degrade plant cell-wall and storage polysaccharides. It degrades all of the major plant cell wall polysaccharides including crystalline cellulose, mannan and xylan and is able to grow on media when these polysaccharides are the sole carbon and energy source. Unlike anaerobic plant cell wall degrading organisms, the C. japonicus enzymes that target polysaccharides, which are integral to the plant cell wall, are fully secreted into the culture media and do not assembly into large multienzyme cellulosome-like complexes. Approximately one third of these putative proteins are predicted to contain often multiple non-catalytic carbohydrate binding modules (CBMs). It increases catalytic activity by reducing the substrate accessibility problem. The variation in the portfolio of CBMs appended to these hydrolytic enzymes may impact upon the carbohydrate targeting of these biocatalysts and thus influence their substrate specificity. All the predicted plant cell-wall degrading enzymes contain signal peptides and are thus extra-cytoplasmic. The genome sequence of C. japonicus reveals a remarkable similarity between the plant cell-wall degrading apparatus of C. japonicus and that of the marine bacterium Saccharophagus degradans. Plant cell-wall degrading enzymes are widely used in the biotechnology sector for the production of detergents, paper, textiles, animal and human foods, however, the most important application of these biocatalysts is in the production of renewable biofuels. Therefore, the discovery of new and more efficient plant cell-wall degrading enzymes can potentially have numerous and important biotechnology applications. (EBI Integr8)

Taxonomy

KingdomPseudomonadati
PhylumPseudomonadota
ClassGammaproteobacteria
OrderCellvibrionales
FamilyCellvibrionaceae
GenusCellvibrio
SpeciesCellvibrio japonicus
StrainUeda107

Profile

Physiology
Gram staining propertiesNegative
ShapeRod
MobilityYes
Flagellar presenceYes
Number of membranes2
Image of Cellvibrio japonicus Ueda107
AI-generated image based on bacteria physiology
Ecology, Host, and Life Cycle
Oxygen requirementsAerobe
Optimal temperatureNot Available
Temperature rangeMesophilic
HabitatTerrestrial
Biotic relationshipFree living
Host(s)Not Available
Cell arrangementNot Available
Sporulationnon-spore-forming
Energy sourceorganotroph; chemotroph
PathogenicityNo

Genome Summary

Cellvibrio japonicus Ueda107


Gene Summary

Adenine Count

1101642 bp

Thymine Count

1095514 bp

Guanine Count

1184709 bp

Cytosine Count

1194708 bp

Genome Length

4576573 bp

Protein-coding Genes

3639 genes

Non-Coding Genes

61 genes

# of Chromosomes/Plasmids

1

Genes

NameLocus TagUniProtStrandCoordinatesMolecular Weight
chromosomal replication initiator protein dnaaCJA_RS00005Not Available+10 - 160559168.9
dna polymerase iii subunit betaCJA_RS00010Not Available+1676 - 277940736.0
dna replication/repair protein recfCJA_RS00015Not Available+2813 - 391041950.8
dna topoisomerase (atp-hydrolyzing) subunit bCJA_RS00020Not Available+3980 - 640089706.0
hypothetical proteinCJA_RS19515Not Available+6530 - 67036657.82
alpha-amylase family glycosyl hydrolaseCJA_RS00025Not Available-6857 - 9640101277.0
pkd domain-containing proteinCJA_RS00030Not Available+10299 - 1228469044.8
sigma-54 interaction domain-containing proteinCJA_RS00035Not Available-12342 - 1390157946.2
cmpa/nrta family abc transporter substrate-binding proteinCJA_RS00040Not Available+14174 - 1561653527.0
nitrate abc transporter permeaseCJA_RS00045Not Available+15619 - 1644630143.5

Displaying genes 1 – 10 of 3700 in total

Pathways

0 pathways

No pathways found

No metabolic pathways have been associated with this bacterium yet.

Metabolites

1746 records
Metabolite IDMetabolite nameStructureCAS number
BASm0000237(R)-4'-phosphopantothenateC9H18NO8PChemical structure of (R)-4'-phosphopantothenateNot available
Average299.2149Da
Monoisotopic299.0770031Da
BASm00002502,5-didehydro-D-gluconateC6H7O7Chemical structure of 2,5-didehydro-D-gluconate53736-12-2
Average191.1156Da
Monoisotopic191.019177578Da
BASm00002532-oxopent-4-enoateC5H5O3Chemical structure of 2-oxopent-4-enoateNot available
Average113.093Da
Monoisotopic113.024417601Da
BASm00002603alpha,7alpha-dihydroxy-12-oxo-5beta-cholanateC24H37O5Chemical structure of 3alpha,7alpha-dihydroxy-12-oxo-5beta-cholanateNot available
Average405.556Da
Monoisotopic405.264647871Da
BASm0000274aldehydo-D-galacturonateC6H9O7Chemical structure of aldehydo-D-galacturonateNot available
Average193.132Da
Monoisotopic193.0353762Da
BASm0000377(S)-malateC4H4O5Chemical structure of (S)-malateNot available
Average132.0716Da
Monoisotopic132.005873238Da
BASm0000387(6R)-5,10-methylene-5,6,7,8-tetrahydrofolateC20H21N7O6Chemical structure of (6R)-5,10-methylene-5,6,7,8-tetrahydrofolateNot available
Average455.432Da
Monoisotopic455.1564286Da
BASm00004283-oxoadipateC6H6O5Chemical structure of 3-oxoadipateNot available
Average158.11Da
Monoisotopic158.022620453Da
BASm0000553biphenyl-2,3-diolC12H10O2Chemical structure of biphenyl-2,3-diolNot available
Average186.2066Da
Monoisotopic186.0680796Da
BASm0000592(S)-1-phenylethanolC8H10OChemical structure of (S)-1-phenylethanolNot available
Average122.1644Da
Monoisotopic122.0731649Da

Displaying 1–10 of 1746 metabolites