trehalose catabolism in Microvirga lotononidis WSM3557

GapMind for catabolism of small carbon sources

trehalose catabolism in Microvirga lotononidis WSM3557

Best path

Rules

Overview: Trehalose degradation is based on MetaCyc pathways I via trehalose-6-phosphate hydrolase (link), II via cytoplasmic trehalase (link), III via trehalose-6-phosphate phosphorylase (link), IV via inverting trehalose phosphorylase (link), V via trehalose phosphorylase (link), VI via periplasmic trehalase (link), as well as trehalose degradation via 3-ketotrehalose (PMID:33657378).

all:

trehalose-3-dehydrogenase, klh and glucose-utilization
or treF and glucose-utilization
or trehalose-PTS, treC and glk
or trehalose-transport, treF and glk
or trehalose-PTS, trePP and pgmB
or trehalose-transport, treP, pgmB and glk
or trehalose-transport, PsTP, pgmA and glk
Comment: In the 3-ketotrehalose pathway, a periplasmic dehydrogenase forms 3-ketotrehalose, a periplasmic 3-ketoglycoside hydrolase (klh) forms glucose and 3-ketoglucose, and the glucose is taken up and utilized; the fate of the 3-ketoglucose is not well understood, but its utilization might not be necessary. In pathway VI, a periplasmic trehalase forms glucose, which is utilized. In pathway I, after uptake and phosphorylation by the PTS, trehalose 6-phosphate hydrolase (treC) forms D-glucose 6-phosphate and D-glucose, and glucokinase (glk) phosphorylates the glucose. In pathway II, a cytoplasmic trehalase cleaves trehalose to two glucose, followed by phosphorylation by glk. In pathway III, after uptake and phosphorylation by the PTS, trehalose-6-phosphate phosphorylase (trePP) forms beta-glucose-1-phosphate and glucose-6-phosphate, and beta-phosphoglucomutase converts glucose-1-phosphate to glucose-6-phosphate. In pathway IV, a secreted inverting trehalose phoshorylase (treP) forms beta-glucose 1-phosphate and glucose; the beta-D-glucose is consumed by beta-phosphoglucomutase. In pathway V, trehalose phosphorylase forms alpha-glucose-1-phosphate and glucose; these are converted to glucose-6-P by alpha-phosphoglucomutase (pgmA) and glk. (This is a fungal pathway and might not occur in prokaryotes.)

trehalose-3-dehydrogenase:

BT2158
or lacA, lacC and lacB

glucose-utilization:

glucose-transport and glk
or glucose-PTS
or gdh, gnl, gadh1, gadh2, gadh3, kguT, kguK, kguD, edd and eda
Comment: Glucose can be taken up and then phosphorylated to glucose 6-phosphate by the kinase glk. Or, both uptake and phosphorylation are catalyzed by a PTS system. Or, glucose is oxidized to glucono-1,5-lactone in the periplasm (by gdh), hydrolyzed to gluconate (by gnl), oxidized to 2-ketogluconate (by gadh123), taken up by kguT, phosphorylated to 2-dehydro-6-phosphogluconate (by kguK), reduced to gluconate 6-phosphate (by kguD), dehydrated by edd to 2-dehydro-3-deoxy-gluconate 6-phosphate, and cleaved by aldolase eda to pyruvate and D-glyceraldehyde 3-phosphate.

glucose-PTS:

ptsG-crr
or bglF
or ptsG and crr
or manX, manY and manZ

glucose-transport:

MFS-glucose
or SSS-glucose
or glcU'
or PAST-A
or SemiSWEET
or SWEET1
or mglA, mglB and mglC
or gtsA, gtsB, gtsC and gtsD
or glcS, glcT, glcU and glcV
or aglE', aglF', aglG' and aglK'
Comment: Transporters and PTS systems were analyzed uzing query: transporter:glucose:D-glucose:D-glucopyranose:ALPHA-GLUCOSE:GLC:CPD-15374

trehalose-transport:

thuE, thuF, thuG and thuK
or lpqY, thuF, thuG and thuK
or malE2, malF1, malG1 and thuK
or malF, malG, malK and malX
or treS, treT, treU and treV
or aglE, aglF, aglG and aglK
or TRET1
Comment: Transporters and PTS systems were identified using query: transporter:trehalose:D-trehalose

trehalose-PTS: treEIIA and treB

Comment: PTS systems form trehalose 6-phosphate. E. coli has EII-BC treB; crr is the EII-A. B. subtilis has EII-BC treP. PMC6148471 shows that ptsG is the predominant EII-A but gamP and ptsA also function. Listeria monocytogenes has EII-BC; the EII-A is not known. Pseudomonas simiae WCS417 and P. fluorescens FW300-N2E3 have similar systems but only EII-A is annotated. In FW300-N2E3, AO353_15980 (A0A0N9WDQ5) is the II-BC protein. In WCS417, PS417_23050 (A0A1N7UR85) is the II-BC protein. These are both similar to E. coli treB.

74 steps (39 with candidates)

Or see definitions of steps

Step	Description	Best candidate	2nd candidate
treF	trehalase	MICLODRAFT_RS27805
mglA	glucose ABC transporter, ATP-binding component (MglA)	MICLODRAFT_RS20890	MICLODRAFT_RS26195
mglB	glucose ABC transporter, substrate-binding component	MICLODRAFT_RS20885	MICLODRAFT_RS16865
mglC	glucose ABC transporter, permease component (MglC)	MICLODRAFT_RS20895	MICLODRAFT_RS16870
glk	glucokinase	MICLODRAFT_RS05260	MICLODRAFT_RS17985
Alternative steps:
aglE	trehalose ABC transporter, substrate-binding component AglE
aglE'	glucose ABC transporter, substrate-binding component (AglE)
aglF	trehalose ABC transporter, permease component 1 (AglF)	MICLODRAFT_RS06455	MICLODRAFT_RS12705
aglF'	glucose ABC transporter, permease component 1 (AglF)	MICLODRAFT_RS06455	MICLODRAFT_RS12705
aglG	trehalose ABC transporter, permease component 2 (AglG)	MICLODRAFT_RS33380	MICLODRAFT_RS27675
aglG'	glucose ABC transporter, permease component 2 (AglG)	MICLODRAFT_RS29400	MICLODRAFT_RS11160
aglK	trehalose ABC trehalose, ATPase component AglK	MICLODRAFT_RS24390	MICLODRAFT_RS24000
aglK'	glucose ABC transporter, ATPase component (AglK)	MICLODRAFT_RS24390	MICLODRAFT_RS24000
bglF	glucose PTS, enzyme II (BCA components, BglF)
BT2158	periplasmic trehalose 3-dehydrogenase (BT2158)
crr	glucose PTS, enzyme IIA
eda	2-keto-3-deoxygluconate 6-phosphate aldolase	MICLODRAFT_RS14220	MICLODRAFT_RS21670
edd	phosphogluconate dehydratase	MICLODRAFT_RS14215	MICLODRAFT_RS25410
gadh1	gluconate 2-dehydrogenase flavoprotein subunit	MICLODRAFT_RS17080
gadh2	gluconate 2-dehydrogenase cytochrome c subunit	MICLODRAFT_RS23090
gadh3	gluconate 2-dehydrogenase subunit 3	MICLODRAFT_RS17075
gdh	quinoprotein glucose dehydrogenase	MICLODRAFT_RS21400	MICLODRAFT_RS15830
glcS	glucose ABC transporter, substrate-binding component (GlcS)
glcT	glucose ABC transporter, permease component 1 (GlcT)	MICLODRAFT_RS21720
glcU	glucose ABC transporter, permease component 2 (GlcU)	MICLODRAFT_RS06010	MICLODRAFT_RS07595
glcU'	Glucose uptake protein GlcU
glcV	glucose ABC transporter, ATPase component (GclV)	MICLODRAFT_RS17555	MICLODRAFT_RS06000
gnl	gluconolactonase	MICLODRAFT_RS13840	MICLODRAFT_RS17620
gtsA	glucose ABC transporter, substrate-binding component (GtsA)	MICLODRAFT_RS33390
gtsB	glucose ABC transporter, permease component 1 (GtsB)	MICLODRAFT_RS33385	MICLODRAFT_RS05270
gtsC	glucose ABC transporter, permease component 2 (GtsC)	MICLODRAFT_RS33380	MICLODRAFT_RS05265
gtsD	glucose ABC transporter, ATPase component (GtsD)	MICLODRAFT_RS05250	MICLODRAFT_RS16810
kguD	2-keto-6-phosphogluconate reductase	MICLODRAFT_RS07715	MICLODRAFT_RS18485
kguK	2-ketogluconokinase
kguT	2-ketogluconate transporter
klh	3-ketotrehalose hydrolase
lacA	periplasmic trehalose 3-dehydrogenase, LacA subunit
lacB	periplasmic trehalose 3-dehydrogenase, cytochrome c subunit (LacB)
lacC	periplasmic trehalose 3-dehydrogenase, LacC subunit
lpqY	trehalose ABC transporter, substrate-binding lipoprotein component LpqY
malE2	trehalose ABC transporter, substrate-binding component MalE2
malF	trehalose ABC transporter, permease component 1 (MalF)	MICLODRAFT_RS12650
malF1	trehalose ABC transporter, permease component 1
malG	trehalose ABC transporter, permease component 2 (MalG)	MICLODRAFT_RS29400	MICLODRAFT_RS12860
malG1	trehalose ABC transporter, permease component 2 (MalG1/MalG2)
malK	trehalose ABC transporter, ATPase component MalK	MICLODRAFT_RS16810	MICLODRAFT_RS05250
malX	trehalose ABC transporter, substrate-binding component MalX
manX	glucose PTS, enzyme EIIAB
manY	glucose PTS, enzyme EIIC
manZ	glucose PTS, enzyme EIID
MFS-glucose	glucose transporter, MFS superfamily
PAST-A	proton-associated sugar transporter A
pgmA	alpha-phosphoglucomutase	MICLODRAFT_RS17825	MICLODRAFT_RS19095
pgmB	beta-phosphoglucomutase
PsTP	trehalose phosphorylase
ptsG	glucose PTS, enzyme IICB
ptsG-crr	glucose PTS, enzyme II (CBA components, PtsG)
SemiSWEET	Sugar transporter SemiSWEET	MICLODRAFT_RS27860
SSS-glucose	Sodium/glucose cotransporter
SWEET1	bidirectional sugar transporter SWEET1
thuE	trehalose ABC transporter, substrate-binding component ThuE	MICLODRAFT_RS24405
thuF	trehalose ABC transporter, permease component 1 (ThuF)	MICLODRAFT_RS12650	MICLODRAFT_RS24400
thuG	trehalose ABC transporter, permease component 2 (ThuG)	MICLODRAFT_RS24395	MICLODRAFT_RS29400
thuK	trehalose ABC transporter, ATPase component ThuK	MICLODRAFT_RS17555	MICLODRAFT_RS05250
treB	trehalose PTS system, EII-BC components TreB
treC	trehalose-6-phosphate hydrolase
treEIIA	N-acetylglucosamine phosphotransferase system, EII-A component (Crr/PtsG/YpqE/GamP)	MICLODRAFT_RS28115
treP	trehalose phosphorylase, inverting
trePP	trehalose-6-phosphate phosphorylase
treS	trehalose ABC transporter, substrate-binding comopnent TreS
treT	trehalose ABC transporter, permease component 1 (TreT)	MICLODRAFT_RS11115	MICLODRAFT_RS16800
TRET1	facilitated trehalose transporter Tret1
treU	trehalose ABC transporter, permease component 2 (TreU)	MICLODRAFT_RS12655	MICLODRAFT_RS12860
treV	trehalose ABC transporter, ATPase component TreV	MICLODRAFT_RS06000	MICLODRAFT_RS11155

Confidence: high confidence medium confidence low confidence
transporter – transporters and PTS systems are shaded because predicting their specificity is particularly challenging.

This GapMind analysis is from Sep 24 2021. The underlying query database was built on Sep 17 2021.

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Candidates (tab-delimited)
Steps (tab-delimited)
Rules (tab-delimited)
Protein sequences (fasta format)
Organisms (tab-delimited)
SQLite3 databases

Related tools

About GapMind

Each pathway is defined by a set of rules based on individual steps or genes. Candidates for each step are identified by using ublast (a fast alternative to protein BLAST) against a database of manually-curated proteins (most of which are experimentally characterized) or by using HMMer with enzyme models (usually from TIGRFam). Ublast hits may be split across two different proteins.

A candidate for a step is "high confidence" if either:

ublast finds a hit to a characterized protein at above 40% identity and 80% coverage, and bits >= other bits+10.
- (Hits to curated proteins without experimental data as to their function are never considered high confidence.)
HMMer finds a hit with 80% coverage of the model, and either other identity < 40 or other coverage < 0.75.

where "other" refers to the best ublast hit to a sequence that is not annotated as performing this step (and is not "ignored").

Otherwise, a candidate is "medium confidence" if either:

ublast finds a hit at above 40% identity and 70% coverage (ignoring otherBits).
ublast finds a hit at above 30% identity and 80% coverage, and bits >= other bits.
HMMer finds a hit (regardless of coverage or other bits).

Other blast hits with at least 50% coverage are "low confidence."

Steps with no high- or medium-confidence candidates may be considered "gaps." For the typical bacterium that can make all 20 amino acids, there are 1-2 gaps in amino acid biosynthesis pathways. For diverse bacteria and archaea that can utilize a carbon source, there is a complete high-confidence catabolic pathway (including a transporter) just 38% of the time, and there is a complete medium-confidence pathway 63% of the time. Gaps may be due to:

our ignorance of proteins' functions,
omissions in the gene models,
frame-shift errors in the genome sequence, or
the organism lacks the pathway.

GapMind relies on the predicted proteins in the genome and does not search the six-frame translation. In most cases, you can search the six-frame translation by clicking on links to Curated BLAST for each step definition (in the per-step page).

For more information, see:

the paper from 2019 on GapMind for amino acid biosynthesis
the paper from 2022 on GapMind for carbon sources
the source code
instructions for running GapMind on your computer

If you notice any errors or omissions in the step descriptions, or any questionable results, please let us know

by Morgan Price, Arkin group, Lawrence Berkeley National Laboratory

GapMind for catabolism of small carbon sources