Unknown

Dataset Information

0

Insights into the biosynthesis of septacidin l-heptosamine moiety unveils a VOC family sugar epimerase.


ABSTRACT: l-Heptopyranoses are important components of bacterial polysaccharides and biological active secondary metabolites like septacidin (SEP), which represents a group of nucleoside antibiotics with antitumor, antifungal, and pain-relief activities. However, little is known about the formation mechanisms of those l-heptose moieties. In this study, we deciphered the biosynthetic pathway of the l,l-gluco-heptosamine moiety in SEPs by functional characterizing four genes and proposed that SepI initiates the process by oxidizing the 4'-hydroxyl of l-glycero-α-d-manno-heptose moiety of SEP-328 (2) to a keto group. Subsequently, SepJ (C5 epimerase) and SepA (C3 epimerase) shape the 4'-keto-l-heptopyranose moiety by sequential epimerization reactions. At the last step, an aminotransferase SepG installs the 4'-amino group of the l,l-gluco-heptosamine moiety to generate SEP-327 (3). An interesting phenomenon is that the SEP intermediates with 4'-keto-l-heptopyranose moieties exist as special bicyclic sugars with hemiacetal-hemiketal structures. Notably, l-pyranose is usually converted from d-pyranose by bifunctional C3/C5 epimerase. SepA is an unprecedented monofunctional l-pyranose C3 epimerase. Further in silico and experimental studies revealed that it represents an overlooked metal dependent-sugar epimerase family bearing vicinal oxygen chelate (VOC) architecture.

SUBMITTER: Chen M 

PROVIDER: S-EPMC9978623 | biostudies-literature | 2023 Feb

REPOSITORIES: biostudies-literature

altmetric image

Publications

Insights into the biosynthesis of septacidin l-heptosamine moiety unveils a VOC family sugar epimerase.

Chen Meng M   Guo Zhengyan Z   Sun Jinyuan J   Tang Wei W   Wang Min M   Tang Yue Y   Li Pengwei P   Wu Bian B   Chen Yihua Y  

Acta pharmaceutica Sinica. B 20220603 2


l-Heptopyranoses are important components of bacterial polysaccharides and biological active secondary metabolites like septacidin (SEP), which represents a group of nucleoside antibiotics with antitumor, antifungal, and pain-relief activities. However, little is known about the formation mechanisms of those l-heptose moieties. In this study, we deciphered the biosynthetic pathway of the l,l-gluco-heptosamine moiety in SEPs by functional characterizing four genes and proposed that SepI initiates  ...[more]

Similar Datasets

| S-EPMC3145628 | biostudies-literature
| S-EPMC6482925 | biostudies-literature
| S-EPMC4594662 | biostudies-literature
| S-EPMC6954431 | biostudies-literature
| S-EPMC11921335 | biostudies-literature
| S-EPMC1172827 | biostudies-literature
| S-EPMC6222537 | biostudies-literature
| S-EPMC3115369 | biostudies-literature
| S-EPMC8152690 | biostudies-literature
| S-EPMC9636800 | biostudies-literature