Acinetobacter pittii

Gram-negativeRodNon-motileAerobe

Kingdom

Pseudomonadati

Phylum

Pseudomonadota

Class

Gammaproteobacteria

Order

Moraxellales

Family

Moraxellaceae

Genus

Acinetobacter

Description

Acinetobacter pittii is a Gram-negative, rod-shaped bacterium that thrives in moderate-temperature environments and is classified as a chemoheterotroph. This organism is predominantly found in various body sites, including the skin, respiratory tract, and gastrointestinal tract, making it a common inhabitant of human microbiota. As a facultative anaerobe, A. pittii demonstrates versatility in oxygen utilization, enabling it to survive in both aerobic and anaerobic environments. The Gram-negative characteristic of A. pittii signifies its cell wall structure, which comprises a thin peptidoglycan layer sandwiched between two membranes. This unique structure not only influences its staining characteristics but also contributes to its pathogenic potential, as it can resist certain antibiotics. The rod shape of A. pittii is significant for its motility and ability to form biofilms, enhancing its survival in various environments and on surfaces, particularly in healthcare settings. As a chemoheterotroph, A. pittii relies on organic compounds as its primary source of carbon and energy, utilizing a range of nutrients in its environment. Its facultative anaerobic capabilities allow it to adapt to fluctuating oxygen levels, which is particularly advantageous in human tissues where oxygen availability may vary.Acinetobacter pittii is notable for its emerging role in human infections, particularly in immunocompromised patients. It has been increasingly associated with nosocomial infections, including ventilator-associated pneumonia and bloodstream infections. Its ability to acquire resistance to multiple antibiotics has made A. pittii a significant concern in clinical microbiology, highlighting the need for ongoing surveillance and innovative treatment strategies. Furthermore, its genetic adaptability makes it an interesting subject for studies in microbial evolution and resistance mechanisms.

Taxonomy

KingdomPseudomonadati
PhylumPseudomonadota
ClassGammaproteobacteria
OrderMoraxellales
FamilyMoraxellaceae
GenusAcinetobacter
SpeciesAcinetobacter pittii
StrainNo strain

Profile

Physiology
Gram staining propertiesNegative
ShapeRod
MobilityNo
Flagellar presenceYes
Number of membranes2
Image of Acinetobacter pittii
Ecology, Host, and Life Cycle
Oxygen requirementsAerobe
Optimal temperature37
Temperature rangeMesophilic
HabitatMultiple
Biotic relationshipFree living
Host(s)Not Available
Cell arrangementSingles
SporulationNot Available
Energy sourceHeterotroph - Chemoheterotroph
PathogenicityHuman

Genome Summary

Acinetobacter pittii

Accession NumberUFIV00000000.1

Gene Summary

Adenine Count

1226561 bp

Thymine Count

1226832 bp

Guanine Count

783949 bp

Cytosine Count

773891 bp

Genome Length

4011234 bp

Protein-coding Genes

3683 genes

Non-Coding Genes

212 genes

# of Chromosomes/Plasmids

11

Genes

NameLocus TagUniProtStrandCoordinatesMolecular Weight
membrane protein insertase yidcI6L29_15920C1DNF7-3369141 - 337090165593.5
membrane protein insertion efficiency factor yiddI6L29_15925B7H341-3370907 - 337122712206.0
ribonuclease p protein componentI6L29_15930B0V5R2-3371238 - 337163015041.3
50s ribosomal protein l34I6L29_15935Q6F6K7-3371660 - 33717945175.51
chromosomal replication initiator protein dnaaI6L29_15940B7GUX5+3372476 - 337388552700.7
dna polymerase iii subunit betaI6L29_15945P0A120+3373983 - 337513142521.2
dna replication/repair protein recfI6L29_15950B7GUX7+3375146 - 337622841120.5
dna topoisomerase (atp-hydrolyzing) subunit bI6L29_15955P0AES7+3376281 - 337874992150.0
cytochrome b562I6L29_15960Q8CVG7+3378785 - 337917714387.5
hypothetical proteinI6L29_15965Not Available+3379313 - 338023935522.9

Displaying genes 25711 – 25720 of 26333 in total

Pathways

92 pathways

Metabolites

0 records
Metabolite IDMetabolite nameStructureCAS number
No metabolites foundTry different search terms or mass values.

Displaying 0 metabolites