Next Article in Journal
Marine Antibiotics 2020
Previous Article in Journal
Distribution of the Water-Soluble Astaxanthin Binding Carotenoprotein (AstaP) in Scenedesmaceae
 
 
Search for Articles:
Title / Keyword
Author / Affiliation / Email
Journal
Article Type
 
 
Advanced Search
 
Section
Special Issue
Volume
Issue
Number
Page
 
Journals
Marine Drugs
Volume 19
Issue 6
10.3390/md19060350
marinedrugs-logo
Submit to this Journal Review for this Journal Propose a Special Issue
► Article Menu

Article Menu

share Share announcement Help format_quote Cite question_answer Discuss in SciProfiles thumb_up
...
Endorse textsms
...
Comment
first_page
settings
Order Article Reprints
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Review

Microbial Oligosaccharides with Biomedical Applications

by
Jian-Lin Xu
1,2,3,†,
Zhi-Feng Liu
1,2,†,
Xiao-Wei Zhang
1,
Hai-Li Liu
1,* and
Yong Wang
1,*
1
Key Laboratory of Synthetic Biology, CAS Center for Excellence in Molecular Plant Sciences, Institute of Plant Physiology and Ecology, Chinese Academy of Sciences, Shanghai 200032, China
2
University of Chinese Academy of Sciences, Beijing 100039, China
3
State Key Laboratory of Bioreactor Engineering, East China University of Science and Technology, Shanghai 200237, China
*
Authors to whom correspondence should be addressed.
†
These authors contributed equally to this work.
Mar. Drugs 2021, 19(6), 350; https://doi.org/10.3390/md19060350
Submission received: 21 May 2021 / Revised: 9 June 2021 / Accepted: 16 June 2021 / Published: 21 June 2021
Browse Figures
Versions Notes

Abstract

:
Microbial oligosaccharides have been regarded as one of the most appealing natural products attributable to their potent and selective bioactivities, such as antimicrobial activity, inhibition of α-glucosidases and lipase, interference of cellular recognition and signal transduction, and disruption of cell wall biosynthesis. Accordingly, a handful of bioactive oligosaccharides have been developed for the treatment of bacterial infections and type II diabetes mellitus. Given that naturally occurring oligosaccharides have increasingly gained recognition in recent years, a comprehensive review is needed. The current review highlights the chemical structures, biological activities and divergent biosynthetic origins of three subgroups of oligomers including the acarviosine-containing oligosaccharides, saccharomicins, and orthosomycins.

1. Introduction

Oligosaccharide chains are ubiquitous across the natural world, which can be found in plants, marine algae, and microorganisms, especially the filamentous bacteria of the order of Actinomycetes. Despite the majority of oligosaccharide chains are present in glycoproteins and glycolipids, they are also found in natural products. It has been demonstrated that the formation of oligosaccharide chains is a fundamental determinant of bioactivity for many secondary metabolites, which is capable of improving or broadening their therapeutic potential [1,2,3,4].
Natural oligosaccharides are a class of carbohydrates polymers, which are normally composed of two to ten monosaccharide units linked together through glycosidic bonds [5]. Due to the diversity of the monomeric sugars and modified side chains and their flexible sequences of assembly, oligosaccharide natural products tend to possess an abundant structural skeleton, which can be divided into four categories based on their core structures including aminooligosaccharides, saccharomicins, orthosomycins, and moenomycins. Most oligosaccharides have been proved to exert a crucial influence in various biological processes, such as signal transduction, molecular recognition, inhibition of α-glucosidases and lipase, and inhibition of pathogenic bacterial growth. Therefore, a handful of bioactive oligosaccharides have been widely used for the treatment of diseases in humans, animals, and plants [6,7,8].
Nevertheless, the oligomeric natural products are less prevalent than other classes of compounds and their biosynthesis has not received sufficient attention in the last century, presumably attributable to their relatively complex and heterogeneous structures, trace-level compositions, and less stable backbones, which is more difficult to detect and identify. In the past two decades, the development of liquid chromatography/high-resolution mass spectrometry (LC/HRMS) has brought considerable progress for the structural analysis of oligosaccharides, which enables users to obtain the detailed primary and secondary fragment ions of oligosaccharides including molecular formula, sugar constituent, and the position of the side chains [9,10,11,12]. An increasing number of oligosaccharides with significant biological properties have been rapidly identified with the aid of LC-HRMS technology, which has attracted much attention in studying their unique biosynthetic pathway and developing potential lead compounds. However, the only review with respect to oligosaccharides was published by Emilianne K. McCranie and Brian O. Bachmann in 2014, which described the mode of action and biosynthesis of bioactive oligosaccharide natural products [13]. In recent years, quite a few new members of bioactive oligosaccharide have been reported, but there is no additional review that updates the structures and biosynthesis of this family of natural products.
In the current review, we focus on the chemical structures and biological activities of oligosaccharide natural products isolated from a microorganic system. A total of 99 compounds including 39 aminooligosaccharides, 2 saccharomicins, and 58 orthosomycins have been summarized. Meanwhile, the recent progress of the biosynthetic mechanism of the representative oligomeric metabolites is highlighted, which contributes to discover new oligosaccharides with the aid of genomic mining and enables to provide opportunities to generate oligosaccharides with improved pharmacological properties through rational reengineering. In addition, the mechanisms of action of three oligosaccharides (aminooligosaccharides, saccharomicins, and orthosomycins) were described in detail by the Emilianne K. McCranie and Brian O. Bachmann. Thus, this review will briefly summarize the mode of action of the representative oligosaccharides with new progresses.

2. Acarviosine-Containing Aminooligosaccharides

2.1. Structural Features and Biological Properties

The acarviosine refers to the pseudo-disaccharide core that is composed of an unsaturated C7N cyclohexitol residue (valienamine) and a 4-amino-4,6-dideoxy-d-glucopyranose (4-amino-4-deoxy-d-quinovopyranose) unit. The acarviosine-containing aminooligosaccharides is a relatively new class of natural products exclusively produced by microorganisms, which usually possess one or more pseudo-trisaccharide moiety (moieties) formed by an acarviosine unit and a d-glucopyranose group through an α-(1 → 4) quinovosidic bond, which are further combined with d-glucose units attached to the reducing and non-reducing end through an α-(1 → 4) glycosidic bond [14].
In the course of the screening for new α-glucosidase inhibitors derived from microorganism, the pseudo-oligosaccharidic complex with significant inhibitory effect against α-glucosidases, especially α-amylases and sucrase, was discovered in the culture filtrates of the Actinoplanes strain SE 50. The pseudotetrasaccharide acarbose (1), the major and most active component of the complex, was reported by Schmidt and his coworkers in 1977 (Figure 1), which exhibited conspicuous inhibitory activity against glucoamylase, sucrase, maltase, and dextrinase [15,16]. This represents the first reported example of acarviosine-containing compound. Structurally, acarbose is composed of an unsaturated C7N cyclohexitol, a deoxyhexose, and a maltose. The pivotal substructure acarviosine, consisting of the valienamine and the deoxyhexose, has been postulated to be indispensable for its enzyme inhibitory activity. Since then, the continued research and new discoveries of homologous natural products acquired from the microorganism have been published.
Large-scale fermentation of Streptomyces myxogenes nov. sp. SF-1130 yielded three new metabolites oligostatins C–E (2–4), which represent the saturated pseudo-penta, pseudo-hexa, and pseudo-heptasaccharides fused with a nitrogen containing glycosidic bond. In contrast to the α-glucosidase inhibitors previously reported, the olefinic bond in valienamine moiety was reduced to hydroxy forms, which was determined by spectroscopic analysis and chemical degradation. In addition to the pronounced α-amylase inhibitory activity, these compounds also showed antimicrobial activity towards several Gram-negative bacteria [17,18]. The chemical investigation of Streptomyces dimorphogenes NR320-OM7HB led to the isolation of six components named trestatins A–C (5–7), Ro 09-0766 (8), Ro 09-0767 (9), and Ro 09-0768 (10), all of which have a unique trehalose residue. These compounds exhibited pronounced α-amylase inhibitory activity with the IC50 values ranging from 8.1 to 610 nM [19,20,21]. Additional research on another bacterial strain Streptomyces calvus TM-521 collected in Tokyo produced two oligosaccharides adiposin-1 (11) and adiposin-2 (12). Adiposin-2 was nearly identical with acarbose, except for the replacement of deoxyglucose moiety in acarbose by the glucose ring, which was further supported by the acid hydrolysate of the adiposin complex [22,23,24,25].
Two new oxirane pseudooligosaccharides carrying two epoxide-containing C7N aminocyclitols were identified from Streptomyces galbus subsp. FH 1716 (DSM 3007) and given the trivial name W-46 H and W-46 P (13 and 14) [8,26]. Another two congeners CKD-711 and CKD-711a (15 and 16), sharing one epoxide-pseudoaminosugar unit, were acquired from the soil actinomycete Streptomyces sp. CK-4416 (Figure 2). Compound 15 showed stronger inhibitory activity than its hexameric analog 16 against sucrase, maltase, and α-amylase with IC50 values of 0.5, 2.5, and 78.0 μg/mL, respectively, indicating that multiple glucose units might pose a detrimental effect for bioactivities. Simultaneously, the moderate of antibacterial activity against Comamonas terrigena was reported for compounds 15 and 16 [27,28,29].
The relatively abundant subgroup of natural aminooligosaccharides is the acarviostatins, which is generally termed as acarviostatins followed by a Roman numeral and two numbers. The Roman numeral denotes the number of the pseudo-trisaccharide cores; the middle digit represents the number of glucose residues at the non-reducing end; and the last digit corresponds to the number of glucose units at the reducing end. The arrangement and assembly of the repeating pseudotrisaccharide units with different numbers of d-glucopyranose at the reducing and non-reducing termini yields numerous acarviostatins. A total of eight acarviostatins (17–24) were initially identified from the mixed extract of Streptomyces coelicoflavus ZG0656, all of which were mixed noncompetitive inhibitors of porcine pancreatic α-amylase (PPA) with the inhibition constants (Ki) ranging from 0.008 to 0.346 μM [30,31,32].
The discovery of the acylated acarviostatins has expanded the structural diversity of this family of oligosaccharide. To the best of our knowledge, fifteen acylated aminooligosaccharides have been separated from two different Streptomyces strains. Although five isovalerylated aminooligosaccharides had been purified from culture broths of the soil Streptomyces luteogriseus in 1995, there were several inconsistencies against their corresponding electrospray ionization mass spectrometry (ESIMS) when the researchers rechecked their structures. The extensive spectroscopic analyses including ESI multistage mass spectrometry, 2D NMR technique and chemical conversion resulted in their structural revision, and these oligomers were redesignated as isovalertatins D03 (25), D23 (26), M03 (27), M13 (28), and M23 (29) (Figure 3). This is the first report of the acylated acarviostatins sharing an isovaleryl group at C-D6 [33,34]. At nearly the same time that the structures of isovalertatins were revised, two butylated congeners butytatins M03 and M13 (30 and 31) were isolated from the same Streptomyces strain [35]. Additional investigation on marine-derived Streptomyces sp. HO1518, collected in Yellow Sea, yielded eight new acylated acarviostatins (32–39) and two known analogues (18 and 25). All of them showed promising inhibitory activities against both α-glucosidase and lipase enzymes under the low micromolar concentrations [36,37].
As mentioned above, all of acarviosine-containing aminooligosaccharides exhibited potent inhibitory activities against key digestive enzymes involved in the breakdown of polysaccharides, such as α-amylase, sucrase, maltase, and isomaltase. Much of the research revealed that the number of the pseudo-trisaccharide core and glucose unit attached to the reducing and non-reducing end played a pivotal role in the inhibition potency of digestive enzymes [32,38]. Generally speaking, aminooligosaccharides containing two or three pseudo-trisaccharide units tend to exhibit the most potent α-glucosidase inhibitory activities, among which the inhibitory potencies of aminooligosaccharides with nine to twelve sugar rings is maximally effective. For instance, D6-O-acetyl-acarviostatin II03 (37) possessing two pseudo-trisaccharides was the most potent α-amylase and sucrase inhibitor, with the IC50 values 540-fold and 27-fold stronger than acarbose. In addition, eight acylated aminooligosaccharides (32–39) were detected to possess significant inhibitory effect against pancreatic lipase, amongst which D6-O-isobutyryl-acarviostatin II03 (38) sharing two pseudo-trisaccharide units was the most active lipase inhibitor with the IC50 value of 0.82 μM. It is worth noting that the acylated aminooligosaccharides with lipase inhibitory activity were reported for the first time. Although acarbose failed to show any antibacterial activity, some of aminooligosaccharides had notable inhibitory effects on the growth of various pathogenic bacteria. For example, oligostatins C–E (2–4) were active against Gram negative bacteria, e.g., Shigella sonnei, Escherichia coli, Salmonella typhi, Proteus vulgaris, and Klebsiella pneumonia. Adiposin-2 (12), which closely resembled acarbose, except for the replacement of deoxyglucose in acarbose by the glucose moiety adjacent to the core unit valienamine, exhibited antibacterial activity with some Gram positive bacteria, Gram negative bacteria, and phytopathogenic fungi. Interestingly, when the double bond of valienamine is tailored into its epoxy form in aminooligosaccharides, their antibacterial activity will be altered. The epoxidal aminooligosaccharides CKD-711 and CKD-711a (15 and 16) displayed a highly selective antibacterial activity against Comamonas terrigena ATCC 8461 instead of the Gram negative and Gram positive bacteria tested by comparison with the oligostatins and the adiposins.

2.2. Mode of Action

In 2011, the structures of human pancreatic α-amylase (HPA) in complex with acarviostatins clearly revealed the mode of action of acarviostatins. Consistent with acarbose, acarviostatin I03 underwent hydrolysis, condensation, and transglycosylation reactions, which led to a six-ring rearranged product acarviostatin I21 that bound tightly in the active site of HPA. Quite interestingly, the larger acarviostatins containing repeated pseudo-trisaccharide cores (acarviostatins II03, III03, and IV03) might undergo only hydrolysis reactions, resulting in the generation of the same seven-ring modified product in the HPA active site. The authors demonstrated that the hydrolysis product with seven sugar rings would show the most efficient α-amylase inhibition attributable to the occupation of the full active site [39,40].

2.3. The Biosynthesis of Acarbose and the Acarviostatins

The acarbose and acarviostatins are considered to be the representative members of the aminooligosaccharides family, and their biosynthesis will be briefly summarized in this review. Two known biosynthetic gene clusters of acarbose termed acb-cluster and gac-cluster were identified from Actinoplanes sp. SE50/110 and Streptomyces glaucescens GLA.O, respectively; whereas the presumptive acarviostatin gene cluster (sct-cluster) was revealed in the Streptomyces coelicoflavus ZG0656 in 2012 (Figure 4). The sct-cluster shows high similarity to the acb-cluster, especially several similar structural genes (SctA, SctB, SctC, SctS, SctR, SctU, and SctV) encoding the synthesis of pseudodisaccharidic acarviosyl moiety and ATP-dependent transporter system (SctW, SctX, and SctY) (Table 1). Consequently, in analogy to the acarbose biosynthetic pathway, the biosynthesis of the acarviostatins has been postulated based on the current knowledge of acarbose biosynthesis and the functional annotation of each synthetic gene [41,42,43].
Biochemically, the biosynthesis of valienol-7-phosphate (valienol-7-P) of the acarviostatins is somewhat different from that of acarbose. The origin of the valienamine moiety in acarbose has been established by Floss and coworkers via labeling experiments, which is derived from the pentose phosphate pathway [44]. Then, Piepersberg and his colleagues have demonstrated that the precursor sedo-heptulose-7-phosphate (sedo-heptulose-7-P) is cyclized by the cyclase (AcbC/SctC) to produce 2-epi-5-epi-valiolone, which is then phosphorylated by the phosphotransferase (AcbM) and catalyzed by the isomerase (AcbO) to generate intermediate 5-epi-valiolone-7-P [45,46,47]. The cyclitol dehydrogenase (AcbL) has been proven to catalyze the dehydration at C-5 and C-6 of 5-epi-valiolone-7-P to yield valienone-7-P, which is further modified by the NADPH-dependent oxidoreductase (AcbN) to give valienol-7-P [48]. Due to the lack of homologs of the genes AcbO, AcbL, and AcbN within the sct biosynthetic gene clusters, two unique genes SctJ and SctO in the Streptomyces coelicoflavus ZG0656, together with the gene SctM similar to AcbM, are putatively responsible for an alternative biosynthesis route of valienol-7-P. The intermediate 2-epi-5-epi-valiolone in the pathway of the acarviostatins is proposed to be epimerized by SctJ, which is phosphorylated and dehydrated through the sequential action of SctM and SctO, leading to generate valienol-7-P [43]. The remaining biosynthesis of the pseudodisaccharidic acarviosyl moiety of the acarviostatins is analogous to those of acarbose. It is speculated that AcbU/SctU should be responsible for the second phosphorylation of valienol-7-P to obtain valienol-1,7-diP, and the latter is converted to NDP-valienol-7-P with the aid of AcbR/SctR.
On the other hand, the biosynthesis of the amino-deoxyhexose moiety is derived from d-glucose-1-P as the initial precursor, which is successively catalyzed by AcbA/SctA (dTDP-glucose synthase), AcbB/SctB (4,6-dehydratase), and AcbV/SctV (4-aminotransferase), leading to produce dTDP-4-amino-4,6-dideoxy-d-glucose [49,50]. The resulting amino-deoxyhexose is proposed to converge with C7-cyclitol by AcbS/SctS (glycosyltransferase), which synthesizes pseudodisaccharidic acarviosyl moiety dTDP-acarviose-7-P. The dTDP-acarviose-7-P has been proposed to involve in the glycosylation coded by AcbD, an exclusive acarviose transferase in the acb-cluster that adds a maltose to the substrate to form acarbose-7-P [51]. The transporter system AcbWXY, which is predicted to participate in a recycling mechanism, secretes acarbose-7-P out of the cell and then is dephosphorylated to obtain acarbose. In the biosynthetic pathway for acarviostatins, the glycosyltransferase SctI is predicted to mediate the transformation of phosphorylated pseudodisaccharide into phosphorylated pseudotrisaccharide acarviostatin I00-7-P. Similarly, the putative transporter SctWXY homologous to AcbWXY is accountable for the export of acarviostatin I00-7-P, resulting in the active pseudotrisaccharide core acarviostatin I00. Three extracellular α-amylases (SctE2, Z1, and Z2) may digest starch into different lengths of maltodextrins and connect these maltooligosaccharides to acarviostatin I00. The resulting acarviostatin homologues are reimported back into the cytoplasm by the transporter SctFGH, which is phosphorylated by the kinase SctK. Then, SctQ and SctE1 hydrolyze the glucoses residues attached to pseudotrisaccharide to regenerate acarviostatin I00-7-P. Thereby, the researchers speculate that the strain ZG0656 is capable of transporting hydrolysates of starch into the cell with the use of this recycling mechanism, which may also explain a plethora of acarviostatins, which have been detected in the host [43,52].
Taken together, a putative biosynthetic pathway of acarviostatins including intracellular assembly and extracellular extension has been proposed on the basis of bioinformatic analysis. However, the biochemical functions of every enzyme in the sct-cluster have not been experimentally characterized thus far, which makes it difficult to identify critical biosynthetic bottlenecks of the acarviostatins and increase their titer through metabolic engineering. The acarviostatins, especially the acylated derivatives, are recognized as a subgroup of promising oligosaccharide natural products attributable to their remarkable inhibitory activities against both α-glucosidase and lipase, which has aroused our medical interest to study the biosynthesis of the acylated acarviostatins. The biosynthesis of backbone structure and the assembly of acyl side chains will be revealed in the further studies. Fully understanding the biosynthesis of the acylated acarviostatins contributes to discover new analogues with improved curative effect that have the potential to fight against diabetes and obesity.

3. Saccharomicins

3.1. Structural Features and Biological Properties

A novel class of structurally intriguing oligosaccharides were isolated in 1998 from the mixed extract of a rare actinomycete Saccharothrix espanaensis LL-C19004 and termed as the saccharomicins. Only two saccharomicins named saccharomicins A and B (40 and 41) have been reported until now (Figure 5), and their subtle difference of the structure was found in the tenth sugar residue, where the α-rhamnopyranosyl in 40 was replaced by the α-digitoxopyranosyl in 41. Saccharomicins are constructed by a N-(m,p-dihydroxycinnamoyl) taurine aglycone and seventeen 6-deoxy sugars, including a sulfated fucose, four fucoses, four saccharosamines, four 4-epi-vancosamines, and four of a combination of rhamnose(s) and digitoxoses. Interestingly, the fucoses are always coupled with saccharosamines through a unique β-β glycosidic bond, while the glycosidic linkages of digitoxoses are determined as α-configuration. In contrast with all known families of antibiotics, saccharomicins belong to new heptadecaglycoside antibiotics, which displayed conspicuous antibacterial activity against the Gram-positive pathogenic bacteria tested, in particular for all multiply drug-resistant staphylococci strains. In addition, both saccharomicins A and B also exhibited activity, despite it being to a relatively lower extent, against Gram-negative microorganisms [53,54]. These results implied that this unprecedented class of oligosaccharides might have the potential to be utilized as an antibacterial drug candidate, which has immensely fascinated pharmaceutical scientists to conduct extensive research efforts toward their biosynthesis.

3.2. Mode of Action

Until now, the precise mechanism of action of the saccharomicins has not been determined. The mechanistic investigations with Escherichia coli and Bacillus subtilis implied that the primary cellular target of the saccharomicins is associated with the bacterial membrane. Within 10 min of saccharomicin A treatment, the complete, nonspecific inhibitory effect of DNA, RNA, and protein biosynthesis was observed, which indicated that the cell membrane integrity in the bacteria was disrupted. Moreover, the extensive leakage of intracellular potassium from E. coli also revealed the membrane-damaging effects of saccharomicin A, which would lead to bacterial cell lysis [54].

3.3. The Biosynthesis of Saccharomicin A

In 2012, the genome sequence of S. espanaensis DSM 44229T revealed the presence of the saccharomicin biosynthetic gene cluster, which was designated as the sam cluster. This gene cluster harbors five genes necessary for the formation of the aglycone substructure, and eight genes responsible for the production of NDP-sugar precursors. There are ten putative glycosyltransferases (Sam11-20) in the cluster, which is in charge of the assembly of the heptadecasaccharide chain, indicating that several of glycosyltransferases should work iteratively (Figure 6) [55].
Bechthold and colleagues first reported the biosynthesis of the aglycone moiety of the saccharomicins in 2006. They identified the biochemical function of two candidate genes (Sam5 and Sam8) derived from S. espanaensis, which were accountable for caffeic acid biosynthesis. Heterologous expression of Sam8 led to the formation of trans-p-coumaric acid, while coexpression of Sam8 and Sam5 resulted in the production of trans-caffeic acid. The enzyme assay unambiguously revealed that the natural substrate of Sam8 was l-tyrosine rather than l-phenylalanine, simultaneously demonstrating that Sam8 was a tyrosine ammonia-lyase and Sam5 was a 4-coumarate 3-hydroxylase [56]. The gene Sam7 shows similarity to acyl-CoA synthetases, which is thought to catalyze the linkage between caffeate and CoA, resulting in the corresponding thioester caffeoyl-CoA. The product may be fused with taurine to form the entire aglycon via Sam36 that has homology to penicillin amidases [55].
More recently, the assembling mechanism of the heptadecasaccharide chain of saccharomicin A has been reported. Assembly of the saccharide chain has been demonstrated to begin from the reaction of Sam20, which transfers a Fuc to the p-phenol group of aglycone. Sam19 transfers a Sac to the C4-hydroxyl of the first nascent Fuc, which is catalyzed by the cooperative action of Sam20 and Sam19 to form pentaglycan M16-1. Subsequently, a Rha is attached to the pentasaccharide chain M16-1 by Sam16 to obtain M18, which is further modified by the Sac transferase (Sam18) and Fuc transferase (Sam17) to give octaglycoside X17. The saccharide chain is elongated by the repeated glycosylation encoded by Sam16, Sam18, Sam17, and Sam13, resulting in the formation of dodecaglycoside X13. The latter is sequentially glycosylated by the Sam15-catalyzed Dig transfer and the Sam14-catalyzed Eva transfer, which is modified by the Dig transferase (Sam11) to form M12. The last two Eva residues are incorporated into M12 under the repeated actions of Sam12. Finally, authors hypothesize that sulfation of Fuc1 is predominantly completed after the assembly of the oligosaccharide chain, which is attributed to the existence of the sulfated Fuc (sFuc) in heptadecaglycoside [57].
This study uncovered the glycosylation process in the biosynthetic network of the heptadecaglycoside saccharomicin A and described functional dissection of every glycosyltransferase in detail, which would be beneficial to fully understand the biosynthesis of the oligosaccharide antibiotic containing the longest saccharide chain existed in natural products. Meanwhile, it also expanded the ever-increasing knowledge on the biosynthesis of oligomeric secondary metabolites and set the stage for pathway engineering of the saccharomicins and discovery of new drug candidates.

4. Orthosomycins

4.1. Structural Features and Biological Properties

Orthosomycins are recognized as a new family of oligosaccharide antibiotics, which are hallmarked by the presence of one or more unique interglycosidic spirocyclic ortho-δ-lactone (orthoester) linkage(s) between sugar residues. It is generally acknowledged that the rarely observed orthoester linkage is necessary for the antibiotic properties of the orthosomycins. Although the orthosomycin family includes hygromycin B, everninomicin, avilamycin, flambamycin, curamycin, etc., the former three members have been extensively studied, especially in the aspect of their bioactivity and biosynthesis [58,59,60,61,62,63,64,65,66,67,68,69,70,71,72,73,74,75,76,77,78,79,80,81,82]. Herein, restricted by the space, everninomicin (EVN) and avilamycin (AVI) will be mainly discussed in this review.
Although hygromycin B (42) (Figure 7), produced by Streptomyces hygroscopicus, is the first disclosed orthosomycin that possesses one othoster linkage [58], a series of more complicated orthosomycins including EVN and AVI have been published and coined as a new class of antibiotics [59]. Evn D (46), the main component of the fermentation broth of Micromonospora carbonacea var. africana, was identified by Schering-Plough Corporation in 1975 [60]. Since then, Evn D has been utilized as a template for the characterization of other EVN and AVI. Until now, twenty EVN (43–62) (Figure 8) have been purified from wide- or mutant-type M. carbonacea var. africana [59,60,61,62,63,71], while thirty-seven AVI (63–99) (Figure 9) have been isolated from the wide- or mutant-type Streptomyces viridochromogenes Tü57 [59,64,72,73,74,75,76,77,78,79,80,81,82]. Structurally, EVN and AVI share the same seven-sugar core (rings B to H) and characteristic substituted partner including two orthoester linkages located between rings C and D and rings G and H and a methylenedioxy bridge attached to ring H. The major differences between EVN and AVI are attributed to the presence (or absence) of the A-ring nitrosugar and the orsellinic acid in EVN (or in AVI).
Amongst the two subgroups of orthosomycins, heptasaccharide AVI (mainly refer to Avi A, 63) and octasaccharide Evn A (Ziracin, 43) exhibited the most potent activity against multidrug-resistant bacterial pathogens, including penicillin-resistant streptococci, methicillin resistant staphylococci, and vancomycin resistant enterococci, which was thus developed as lead compounds or clinical drugs for the treatment of antibiotic resistant infections [65,66]. Heptasaccharide AVI premix 10% (MaxusG), firstly developed and produced by Eli Lilly, Bad Homburg, Germany, are widely used as antibiotics in animals [67]. Octasaccharide Evn A (Ziracin) advanced to phase III clinical trials, but the unstated pharmacological concerns prevented its clinical approval [68]. Given that EVN and AVI have a unique mechanism distinguish from other known antibiotics by binding to an exclusive site on bacterial ribosome [69,70], continuous searching for new antimicrobial agents originate from EVN and AVI is a meaningful task. Very recently, reconstruction of the wide-type M. carbonacea var. Africana targeting the functional related oxidase encoding genes resulted in the discovery of a new intriguing Evn, Evn P (60), and its two related hydrolysis products, Evns N (61) and O (62) [71], which possess either characteristic full-length EVA or partial A1-A-B-ring conjugated to a macrolide rosamicin via a rare nitrone moiety. Particular interestingly, both the full-length and truncated EVA-rosamicin conjugates, Evn P and Evns N, showed significant activities against S. aureus, which is almost close to Evn A. Moreover, Evn P displayed a dual targeting of orthogonal binding sites (macrolide and orthosomycin) within the ribosome, which is regarded as a hopeful candidate, generating a new type of hybrid ribosome engaging antibiotic to improve pharmacological properties.

4.2. Mode of Action

It is generally understood that the orthosomycin antibiotics EVN and AVI should bind to a unique site on the ribosome, which is different from other ribosome-targeting antibacterial agents currently use in the clinic. In 2016, two research groups disclosed the crystal structures of the EVN and AVI in complex with the bacterial ribosome, which unambiguously demonstrated that both EVN and AVI interacted with arginine residues of ribosomal protein L16 and helices 89 and 91 of the 23S rRNA. This binding site overlaps with the A-site tRNA entrance corridor, which inhibits protein biosynthesis by blocking the binding site of the A-tRNA elbow [69,70].

4.3. The Biosynthesis of Avi A

With the consideration of the immense biomedical potential for AVI and EVN, the unique biosynthetic pathways have been investigated, especially for Avi A. In 1997, the Avi A integral biosynthetic gene cluster with a 60 kb (54 ORF) region was discovered from S. viridochromogenes Tü57 by constructing a cosmid library, probing with an isotopic-labeled bite gene, and screening with southern hybridization [72,73]. The cluster contains genes proposed to be function as precursor biosynthesis, structural modification, skeletal assembly, resistance, transportation, and regulation in AVI biosynthetic pathway. In details, the precursor synthesis genes include aviN, aviM, aviD, aviE1-aviE3, aviS, aviB1, and aviB2. Structural modification genes contain five types, that is, methyltransferase genes aviG1-aviG6, epimerase genes aviQ1-aviQ3, ketoreductase genes aviT and aviZ1-aviZ3, halogenase gene aviH, and S-adenosylmethioninase gene aviX12. The skeletal assembly genes include glycosyltransferase genes aviGT1-aviGT4 and hydroxylase genes aviO1-aviO3. The former is putatively responsible for the assembly of heptasaccharide chain, while the latter may participate in the formation of O-glycosidic and orthoester bonds. In addition, aviRa and aviRb perhaps be related to AVI resistance, aviABC1 and aviABC2 are involved in AVI transport, while aviC1 and aviC2 may act as positive regulators (Table 2).
As mentioned above, the backbone of Avi A is composed of a terminal dichloroisoeverninic acid unit (residue A) and its attachment to a heptasaccharide chain consisting of d-olivose (residues B and C), 2-deoxy-d-evalose (residue D), d-fucose (residue E), d-mannose (residue F), l-lyxose (residue G), and methyleurekanate (residue H). Due to the multiple-ring structure of Avi A, its biosynthetic pathway is relatively complicated. Up to now, aided with the bioinformatics analysis, some of the key enzymes in the Avi A biosynthesis pathway have been successfully elucidated by analysis of the corresponding Avi derivatives, gavibamycins (Gav, 79–99), in situ gene knockout and complementation strategy, heterologous expression systems, such as S. lividans TK24, S. coelicolor CH999, Streptomyces TK66, etc., or feeding experiments [72,73,74,75,76,77,78,79,80,81,82]. Herein, four main initial precursors, including propionyl-CoA, d-glucose-1-phosphate, GDP-d-mannose, and UDP-d-glucose, are summarized in Figure 10. Accordingly, the biosynthesis of the skeletal assembly of the eight moieties A-H in Avi A is divided into four main branches distinguished from each other with colors as shown in Figure 10. Of all the branches, the biosynthesis for moieties A (blue) and F (sub-branch, green) have been fully or almost fully elucidated. For the biosynthesis of moiety A, starting from propionyl-CoA, iterative type I polyketide synthase AviM [72], is responsible for the synthesis of orsellinic acid, which is further catalyzed by methyltransferase AviG4 [73] and halogenase AviH [73] to produce the complete dichloroisoeverninic acid moiety. For the biosynthesis of moieties B–D (orange), the starting precursor, glucose-1-phosphate, is converted to dTDP-d-olivose and dTDP-2-deoxy-d-evalose, respectively, and three enzymes including dTDP-glucose synthase AviD [72], dTDP-glucose 4,6-dehydratase AviE1 [72], and C-methyltransferase AviG1 [74] have been discovered to anticipate the biosynthesis of rings B-D. For the biosynthesis of residues E and H (pink), GDP-d-mannose is their common precursor. Hydroxylase AviO2 [75] combined with pyruvate dehydrogenase AviB1 and AviB2 [75], a heterotetrameric complex protein (α2β2 chains), catalyze the conversion of pyruvate to an acetyl carbanion at C4 in eurekanate moiety (ring H), while O-methyltransferase AviG5 [76] is the answer for the methylation of the C4 hydroxyl group in GDP-d-fucose in ring E; for the biosynthesis of residues F and G (green), their common precursor is UDP-d-glucose. Decarboxylase AviE2 [77] converts UDP-d-glucuronic acid to UDP-d-xylose in ring G, while AviX12 [78], a [Fe-S] cluster containing radical AdoMet enzyme catalyzing an unusual epimerization reaction, together with two O-methyltransferase AviG2 and AviG6 [76], complement the whole biosynthesis of ring F.
As we know, the residues A-H in Avi A are associated by orthoester linkages, glycosidic linkages, ester linkages, and a methylenedioxy bridge. Until now, only the partial linkage between rings G and H have been proved to be catalyzed by glycosyltransferase AviGT4 [77], while the others still remain unknown. Orthoester group as a characteristic pharmacophore of octasaccharides is crucial to the biomedical application of Avi A. Therefore, clarifying the formation of the orthoester group is a continuous target for scientists. Recently, McCulloch [79] have identified a conserved group of nonheme iron, α-ketoglutarate-dependent oxygenases, including AviO1 of AVI and its two homologues, EvdO1 and EvdO2 of EVN and HygX of hygromycin B. Analysis of the high-resolution crystal structures reveals that an orientation of one glycosidic linkage of oxygenase HygX is consistent with metal-catalyzed hydrogen atom abstraction from substrate, supporting that AviO1 participates the catalysis of the orthoester linkages. In addition, two resistances, rRNA-methyltransferase AviRa and AviRb, two regulators, ABC transporters AviABC1 and AviABC2 [80], and two transcriptional activators, AviC1 and AviC2 [81] are also reported. Regarding the Avi A contributes to poor water solubility and difficulties in drug development perhaps ascribed to its multiple methyl groups [76,82], fully understanding the Avi A biosynthetic pathway will provide useful information and contribute to produce novel derivatives with improved polarity and pharmacokinetic properties.

5. Summary and Perspectives

Despite the fact that the first oligosaccharide (hygromycin B) was described in 1958, this family of compounds has received sufficient attention only recently. A small number of bioactive oligosaccharides have been examined in clinical trials or introduced into the drug market for the treatment of infectious diseases and metabolic disorders, such as acarbose (α-amylase inhibitor), hygromycin B and Avi A (veterinary drugs), and Evn A (antimicrobial agent). The most widely used oligosaccharide is acarbose, a pseudotetrasaccharide exhibiting an inhibitory effect on intestinal α-glucosidases such as α-amylase, sucrase, maltase, and isomaltase. It is worth noting that the higher molecular weight acarviostatins, exhibiting more potent activities against α-glucosidases than acarbose, were isolated from the culture broths of various members of the genus Streptomyces, which suggested that this class of compounds could be widely distributed in the marine and terrestrial bacteria. More importantly, the culturable marine-derived actinomycetes are becoming an outstanding source for the discovery of new aminooligosaccharides.
Owing to the structural complexity of oligosaccharide secondary metabolites, especially the fact that each of them has multiple monosaccharides, it is very challenging to obtain those compounds and their analogues by chemical synthesis, which turned the research interest of medical chemists toward their biosynthesis. The efforts on the biosynthesis of oligosaccharide secondary metabolites have revealed several closely related novel biosynthetic pathways exclusively produced by microorganisms. The decipherment of the metabolic pathways of oligomeric natural products is beneficial for shedding more light on their mode of formation and distinguishing biosynthetic features. In the meantime, the wealth of knowledge acquired from research on oligosaccharides biosynthesis has provided new opportunities to produce novel derivatives by means of combinatorial biosynthesis or synthetic biology approaches, which can expand the diversity of oligosaccharides to some extent. In addition, the advances in DNA sequencing, bioinformatics and omics, and molecular genetics in recent years, have enabled the expansion of our understanding of oligosaccharides biosynthesis and the titer improvement of certain microbial pharmaceutical products, which contributes to produce many more of oligomeric analogues for structure–activity relationship studies.

Author Contributions

X.-W.Z. and J.-L.X. searched and collected literature; J.-L.X., H.-L.L. and Z.-F.L. wrote the original draft; H.-L.L. and Y.W. reviewed and edited the manuscript. All authors have read and agreed to the published version of the manuscript.

Funding

This work was supported financially by the National Key R&D Program of China (No. 2018YFA0900600), the Strategic Priority Research Program “Molecular mechanism of Plant Growth and Development” of CAS (Nos. XDB27020202, XDB27020103), the National Natural Science Foundation of China (Grant Nos. 41876084, 31700261, 31670099), the Construction of the Registry and Database of Bioparts for Synthetic Biology of the Chinese Academy of Science (No. ZSYS-016), the Program of Shanghai Academic Research Leader (No. 20XD1404400), the International Partnership Program of Chinese Academy of Science (No. 153D31KYSB20170121), and the National Key Laboratory of Plant Molecular Genetics, SIPPE, CAS.

Institutional Review Board Statement

Not applicable.

Data Availability Statement

Not applicable.

Acknowledgments

We sincerely thank Shi-Zheng Bu and Yi-Ning Liu in the Core Facility Center of Institute of Plant Physiology and Ecology, Chinese Academy of Sciences, for their invaluable comments and suggestions.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Cheong, K.L.; Qiu, H.M.; Du, H.; Liu, Y.; Khan, B.M. Oligosaccharides derived from red seaweed: Production, properties, and potential health and cosmetic applications. Molecules 2018, 23, 2451. [Google Scholar] [CrossRef] [Green Version]
  2. Elshahawi, S.I.; Shaaban, K.A.; Kharel, M.K.; Thorson, J.S. A comprehensive review of glycosylated bacterial natural products. Chem. Soc. Rev. 2015, 44, 7591–7697. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  3. De Jesus Raposo, M.F.; de Morais, A.M.B.; de Morais, R.M.S.C. Marine polysaccharides from algae with potential biomedical applications. Mar. Drugs 2015, 13, 2967–3028. [Google Scholar] [CrossRef] [PubMed]
  4. Zhu, B.W.; Ni, F.; Xiong, Q.; Yao, Z. Marine oligosaccharides originated from seaweeds: Source, preparation, structure, physiological activity and applications. Crit. Rev. Food Sci. Nutr. 2021, 61, 60–74. [Google Scholar] [CrossRef] [PubMed]
  5. Bose, S.K.; Howlader, P.; Wang, W.X.; Yin, H. Oligosaccharide is a promising natural preservative for improving postharvest preservation of fruit: A review. Food Chem. 2021, 341, 128178. [Google Scholar] [CrossRef] [PubMed]
  6. Truscheit, E.; Frommer, W.; Junge, B.; Müller, L.; Schmidt, D.D.; Wingender, W. Chemistry and biochemistry of microbial α-glucosidase inhibitors. Angew. Chem. Int. Ed. Engl. 1981, 20, 744–761. [Google Scholar] [CrossRef]
  7. Seeberger, P.H.; Werz, D.B. Synthesis and medical applications of oligosaccharides. Nature 2007, 446, 1046–1051. [Google Scholar] [CrossRef] [PubMed]
  8. Mahmud, T. The C7N aminocyclitol family of natural products. Nat. Prod. Rep. 2003, 20, 137–166. [Google Scholar] [CrossRef]
  9. Carter, G.T. NP/MS since 1970: From the basement to the bench top. Nat. Prod. Rep. 2014, 31, 711–717. [Google Scholar] [CrossRef]
  10. Kersten, R.D.; Ziemert, N.; Gonzalez, D.J.; Duggan, B.M.; Nizet, V.; Dorrestein, P.C.; Moore, B.S. Glycogenomics as a mass spectrometry-guided genome-mining method for microbial glycosylated molecules. Proc. Natl. Acad. Sci. USA 2013, 110, E4407–E4416. [Google Scholar] [CrossRef] [Green Version]
  11. Lang, Y.Z.; Zhao, X.; Liu, L.L.; Yu, G.L. Applications of mass spectrometry to structural analysis of marine oligosaccharides. Mar. Drugs 2014, 12, 4005–4030. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  12. Liu, M.Q.; Zeng, W.F.; Fang, P.; Cao, W.Q.; Liu, C.; Yan, G.Q.; Zhang, Y.; Peng, C.; Wu, J.Q.; Zhang, X.J.; et al. pGlyco 2.0 enables precision N-glycoproteomics with comprehensive quality control and one-step mass spectrometry for intact glycopeptide identification. Nat. Commun. 2017, 8, 438. [Google Scholar] [CrossRef]
  13. McCranie, E.K.; Bachmann, B.O. Bioactive oligosaccharide natural products. Nat. Prod. Rep. 2014, 31, 1026–1042. [Google Scholar] [CrossRef] [Green Version]
  14. Wang, L.Q.; Cui, Q.X.; Hou, Y.Y.; Bai, F.; Sun, J.X.; Cao, X.F.; Liu, P.; Jiang, M.; Bai, G. An integrated strategy of ultra-high-performance liquid chromatography/quadrupole-time-of-flight mass spectrometry and virtual screening for the identification of α-glucosidase inhibitors in acarviostatin-containing complex. J. Chromatogr. A 2013, 1319, 88–96. [Google Scholar] [CrossRef] [PubMed]
  15. Schmidt, D.D.; Frommer, W.; Junge, B.; Müller, L.; Wingender, W.; Truscheit, E.; Schäfer, D. α-Glucosidase inhibitors. New complex oligosaccharides of microbial origin. Naturwissenschaften 1977, 64, 535–536. [Google Scholar] [CrossRef] [PubMed]
  16. Krentz, A.J.; Bailey, C.J. Oral antidiabetic agents: Current role in type 2 diabetes mellitus. Drugs 2005, 65, 385–411. [Google Scholar] [CrossRef]
  17. Itoh, J.; Omoto, S.; Shomura, T.; Ogino, H.; Iwamatsu, K.; Inouye, S.; Hidaka, H. Oligostatins, new antibiotics with amylase inhibitory activity. I. Production, isolation and characterization. J. Antibiot. 1981, 34, 1424–1428. [Google Scholar] [CrossRef] [Green Version]
  18. Omoto, S.; Itoh, J.; Ogino, H.; Iwamatsu, K.; Nishizawa, N.; Inouye, S. Oligostatins, new antibiotics with amylase inhibitory activity. II. Structures of oligostatins C, D, and E. J. Antibiot. 1981, 34, 1429–1433. [Google Scholar] [CrossRef] [Green Version]
  19. Yokose, K.; Ogawa, K.; Sano, T.; Watanabe, K.; Maruyama, H.B.; Suhara, Y. New α-amylase inhibitor, trestatins. I. Isolation characterization and biological activities of trestatins A, B, and C. J. Antibiot. 1983, 36, 1157–1165. [Google Scholar] [CrossRef] [Green Version]
  20. Yokose, K.; Ogawa, K.; Suzuki, Y.; Umeda, I.; Suhara, Y. New α-amylase inhibitor, trestatins. II. Structure determination of trestatins A, B and C. J. Antibiot. 1983, 36, 1166–1175. [Google Scholar] [CrossRef] [Green Version]
  21. Yokose, K.; Ogawa, M.; Ogawa, K. New alpha-amylase inhibitor, trestatins. III. Structure determination of new trestatin components Ro 09-0766, Ro 09-0767 and Ro 09-0768. J. Antibiot. 1984, 37, 182–186. [Google Scholar] [CrossRef] [PubMed]
  22. Namiki, S.; Kangouri, K.; Nagate, T.; Hara, H.; Sugita, K.; Omura, S. Studies on the alpha-glucoside hydrolase inhibitor, adiposin. I. Isolation and physicochemical properties. J. Antibiot. 1982, 35, 1234–1236. [Google Scholar] [CrossRef] [Green Version]
  23. Namiki, S.; Kangouri, K.; Nagate, T.; Hara, H.; Sugita, K.; Omura, S. Studies on the alpha-glucoside hydrolase inhibitor, adiposin. II. Taxonomic studies on the producing microorganism. J. Antibiot. 1982, 35, 1156–1159. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  24. Kangouri, K.; Namiki, S.; Nagate, T.; Hara, H.; Sugita, K.; Omura, S. Studies on the alpha-glucoside hydrolase inhibitor, adiposin. III. alpha Glucoside hydrolase inhibitory activity and antibacterial activity in vitro. J. Antibiot. 1982, 35, 1160–1166. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  25. Namiki, S.; Kangouri, K.; Nagate, T.; Hara, H.; Sugita, K.; Noda, K.; Tarumoto, Y.; Omura, S. Studies on the alpha-glucoside hydrolase inhibitor, adiposin. IV. Effect of adiposin on intestinal digestion of carbohydrates in experimental animals. J. Antibiot. 1982, 35, 1167–1173. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  26. Vertesy, L.; Betz, J.; Fehlhaber, H.W.; Geisen, K. Oxirane Pseudooligosaccharides, A Process for Their Preparation, Their Use and Pharmaceutical Preparations. U.S. Patent 4,990,500 A, 5 February 1991. [Google Scholar]
  27. Kim, J.G.; Chang, H.B.; Kwon, Y.I.; Moon, S.K.; Chun, H.S.; Ahn, S.K.; Hong, C.I. Novel alpha-glucosidase inhibitors, CKD-711 and CKD-711a produced by Streptomyces sp. CK-4416. I. Taxonomy, fermentation and isolation. J. Antibiot. 2002, 55, 457–461. [Google Scholar] [CrossRef] [Green Version]
  28. Kwon, Y.I.; Son, H.J.; Moon, K.S.; Kim, J.K.; Kim, J.G.; Chun, H.S.; Ahn, S.K.; Hong, C.I. Novel alpha-glucosidase inhibitors, CKD-711 and CKD-711a produced by Streptomyces sp. CK-4416. II. Biological properties. J. Antibiot. 2002, 55, 462–466. [Google Scholar] [CrossRef] [Green Version]
  29. Chang, H.B.; Kim, S.H.; Kwon, Y.I.; Choung, D.H.; Choi, W.K.; Kang, T.W.; Lee, S.; Kim, J.G.; Chun, H.S.; Ahn, S.K.; et al. Novel alpha-glucosidase inhibitors, CKD-711 and CKD-711a produced by Streptomyces sp. CK-4416. III. Physico-chemical properties and structure elucidation. J. Antibiot. 2002, 55, 467–471. [Google Scholar] [CrossRef] [Green Version]
  30. Geng, P.; Bai, G. Two novel aminooligosaccharides isolated from the culture of Streptomyces coelicoflavus ZG0656 as potent inhibitors of α-amylase. Carbohydr. Res. 2008, 343, 470–476. [Google Scholar] [CrossRef]
  31. Geng, P.; Qiu, F.; Zhu, Y.Y.; Bai, G. Four acarviosin-containing oligosaccharides identified from Streptomyces coelicoflavus ZG0656 are potent inhibitors of α-amylase. Carbohydr. Res. 2008, 343, 882–892. [Google Scholar] [CrossRef]
  32. Geng, P.; Sun, T.; Zhong, Q.P.; Li, X.X.; Shi, L.Y.; Bai, F.; Bai, G. Two novel potent α-amylase inhibitors from the family of acarviostatins isolated from the culture of Streptomyces coelicoflavus ZG0656. Chem. Biodivers. 2013, 10, 452–459. [Google Scholar] [CrossRef]
  33. Zhong, D.; Si, D.Y.; He, W.Y.; Zhao, L.M.; Xu, Q.M. Structural revision of isovalertatins M03, M13, and M23 isolated from the culture of Streptomyces luteogriseus. Carbohydr. Res. 2001, 331, 69–75. [Google Scholar] [CrossRef]
  34. Si, D.Y.; Zhong, D.F.; He, W.Y.; Zhao, L.M. Structural revision of isovalertatins D03 and D23 isolated from the culture filtrate of Streptomyces luteogriseus. Chin. Chem. Lett. 2001, 12, 327–330. [Google Scholar]
  35. Si, D.Y.; Zhong, D.F.; Xu, Q.M. Two butylated aminooligosaccharides isolated from the culture filtrate of Streptomyces luteogriseus. Carbohydr. Res. 2001, 335, 127–132. [Google Scholar] [CrossRef]
  36. Liu, H.L.; E, H.-C.; Xie, D.A.; Cheng, W.B.; Tao, W.Q.; Wang, Y. Acylated aminooligosaccharides with inhibitory effects against α-amylase from Streptomyces sp. HO1518. Mar. Drugs 2018, 16, 403. [Google Scholar] [CrossRef] [Green Version]
  37. Xu, J.L.; Liu, H.L.; Liu, Z.F.; Ren, Y.H.; Wang, Y. Acylated aminooligosaccharides from the yellow sea Streptomyces sp. HO1518 as both α-glucosidase and lipase inhibitors. Mar. Drugs 2020, 18, 576. [Google Scholar] [CrossRef]
  38. Geng, P.; Bai, G.; Shi, Q.; Zhang, L.; Gao, Z.; Zhang, Q. Taxonomy of the Streptomyces strain ZG0656 that produces acarviostatin α-amylase inhibitors and analysis of their effects on blood glucose levels in mammalian systems. J. Appl. Microbiol. 2009, 106, 525–533. [Google Scholar] [CrossRef]
  39. Li, C.M.; Begum, A.; Numao, S.; Park, K.H.; Withers, S.G.; Brayer, G.D. Acarbose rearrangement mechanism implied by the kinetic and structural analysis of human pancreatic alpha-amylase in complex with analogues and their elongated counterparts. Biochemistry 2005, 44, 3347–3357. [Google Scholar] [CrossRef]
  40. Qin, X.H.; Ren, L.M.; Yang, X.; Bai, F.; Wang, L.L.; Geng, P.; Bai, G.; Shen, Y.Q. Structures of human pancreatic α-amylase in complex with acarviostatins: Implications for drug design against type II diabetes. J. Struct. Biol. 2011, 174, 196–202. [Google Scholar] [CrossRef]
  41. Schwientek, P.; Szczepanowski, R.; Rückert, C.; Kalinowski, J.; Klein, A.; Selber, K.; Wehmeier, U.F.; Stoye, J.; Pühler, A. The complete genome sequence of the acarbose producer Actinoplanes sp. SE50/110. BMC Genom. 2012, 13, 112. [Google Scholar] [CrossRef] [Green Version]
  42. Ortseifen, V.; Kalinowski, J.; Pühler, A.; Rückert, C. The complete genome sequence of the actinobacterium Streptomyces glaucescens GLA.O (DSM 40922) carrying gene clusters for the biosynthesis of tetracenomycin C, 5′-hydroxy streptomycin, and acarbose. J. Biotechnol. 2017, 262, 84–88. [Google Scholar] [CrossRef] [PubMed]
  43. Guo, X.; Geng, P.; Bai, F.; Bai, G.; Sun, T.; Li, X.; Shi, L.; Zhong, Q. Draft genome sequence of Streptomyces coelicoflavus ZG0656 reveals the putative biosynthetic gene cluster of acarviostatin family α-amylase inhibitors. Lett. Appl. Microbiol. 2012, 55, 162–169. [Google Scholar] [CrossRef]
  44. Degwert, U.; van Hülst, R.; Pape, H.; Herrold, R.E.; Beale, J.M.; Keller, P.J.; Lee, J.P.; Floss, H.G. Studies on the biosynthesis of the alpha-glucosidase inhibitor acarbose: Valienamine, a m-C7N unit not derived from the shikimate pathway. J. Antibiot. 1987, 40, 855–861. [Google Scholar] [CrossRef] [PubMed]
  45. Mahmud, T.; Tornus, I.; Egelkrout, E.; Wolf, E.; Uy, C.; Floss, H.G.; Lee, S. Biosynthetic studies on the α-glucosidase inhibitor acarbose in Actinoplanes sp.: 2-epi-5-epi-valiolone is the direct precursor of the valienamine moiety. J. Am. Chem. Soc. 1999, 121, 6973–6983. [Google Scholar] [CrossRef]
  46. Stratmann, A.; Mahmud, T.; Lee, S.; Distler, J.; Floss, H.G.; Piepersberg, W. The AcbC protein from Actinoplanes species is a C7-cyclitol synthase related to 3-dehydroquinate synthases and is involved in the biosynthesis of the alpha-glucosidase inhibitor acarbose. J. Biol. Chem. 1999, 274, 10889–10896. [Google Scholar] [CrossRef] [Green Version]
  47. Zhang, C.S.; Stratmann, A.; Block, O.; Brückner, R.; Podeschwa, M.; Altenbach, H.J.; Wehmeier, U.F.; Piepersberg, W. Biosynthesis of the C7-cyclitol moiety of acarbose in Actinoplanes species SE50/110. 7-O-phosphorylation of the initial cyclitol precursor leads to proposal of a new biosynthetic pathway. J. Biol. Chem. 2002, 277, 22853–22862. [Google Scholar] [CrossRef] [Green Version]
  48. Zhao, Q.Q.; Luo, Y.C.; Zhang, X.; Kang, Q.J.; Zhang, D.; Zhang, L.L.; Bai, L.Q.; Deng, Z.X. A severe leakage of intermediates to shunt products in acarbose biosynthesis. Nat. Commun. 2020, 11, 1468. [Google Scholar] [CrossRef] [Green Version]
  49. Wehmeier, U.F.; Piepersberg, W. Biotechnology and molecular biology of the α-glucosidase inhibitor acarbose. Appl. Microbiol. Biotechnol. 2004, 63, 613–625. [Google Scholar] [CrossRef]
  50. Wehmeier, U.F. The biosynthesis and metabolism of acarbose in Actinoplanes sp. SE 50/110: A progress report. Biocatal. Biotransfor. 2003, 21, 279–284. [Google Scholar] [CrossRef]
  51. Rockser, Y.; Wehmeier, U.F. The gac-gene cluster for the production of acarbose from Streptomyces glaucescens GLA.O: Identification, isolation and characterization. J. Biotechnol. 2009, 140, 114–123. [Google Scholar] [CrossRef] [PubMed]
  52. Geng, P.; Meng, X.S.; Bai, G.; Luo, G.A. Profiling of acarviostatin family secondary metabolites secreted by Streptomyces coelicoflavus ZG0656 using ultraperformance liquid chromatography coupled with electrospray ionization mass spectrometry. Anal. Chem. 2008, 80, 7554–7561. [Google Scholar] [CrossRef] [PubMed]
  53. Kong, F.M.; Zhao, N.; Siegel, M.M.; Janota, K.; Ashcroft, J.S.; Koehn, F.E.; Borders, D.B.; Carter, G.T. Saccharomicins, novel heptadecaglycoside antibiotics effective against multidrug-resistant bacteria. J. Am. Chem. Soc. 1998, 120, 13301–13311. [Google Scholar] [CrossRef]
  54. Singh, M.P.; Petersen, P.J.; Weiss, W.J.; Kong, F.; Greenstein, M. Saccharomicins, novel heptadecaglycoside antibiotics produced by Saccharothrix espanaensis: Antibacterial and mechanistic activities. Antimicrob. Agents Chemother. 2000, 44, 2154–2159. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  55. Strobel, T.; Al-Dilaimi, A.; Blom, J.; Gessner, A.; Kalinowski, J.; Luzhetska, M.; Pühler, A.; Szczepanowski, R.; Bechthold, A.; Rückert, C. Complete genome sequence of Saccharothrix espanaensis DSM 44229T and comparison to the other completely sequenced Pseudonocardiaceae. BMC Genom. 2012, 13, 465. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  56. Berner, M.; Krug, D.; Bihlmaier, C.; Vente, A.; Muller, R.; Bechthold, A. Genes and enzymes involved in caffeic acid biosynthesis in the actinomycete Saccharothrix espanaensis. J. Bacteriol. 2006, 188, 2666–2673. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  57. Zhao, J.F.; Mo, T.L.; Li, X.H.; Ding, W.; Zhang, Q. Dissection of the glycosylation in the biosynthesis of the heptadecaglycoside antibiotic saccharomicin A. J. Org. Chem. 2021. [Google Scholar] [CrossRef]
  58. Mann, R.L.; Bromer, W.W. The isolation of a second antibiotic from Streptomyces hygroscopicus. J. Am. Chem. Soc. 1958, 80, 2714–2716. [Google Scholar] [CrossRef]
  59. Wright, D.E. The Orthosomycins, a new family of antibiotics. Tetrahedron 1979, 35, 1207–1237. [Google Scholar] [CrossRef]
  60. Ganguly, A.K.; Sarre, O.Z.; Greeves, D.; Morton, J. Structure of everninomicin D. J. Am. Chem. Soc. 1975, 97, 1982–1985. [Google Scholar] [CrossRef] [PubMed]
  61. Ganguly, A.K.; Sarre, O.; Girijavallabhan, V.M. The structure of new oligosaccharide antibiotics, 13-384 components 1 and 5. Heterocycles 1989, 28, 83–88. [Google Scholar] [CrossRef]
  62. Saksena, A.K.; Jao, E.; Murphy, B.; Schumacher, D.; Chan, T.M.; Puar, M.S.; Jenkins, J.K.; Maloney, D.; Cordero, M.; Pramanik, B.D.; et al. Structure elucidation of SCH 49088, a novel everninomicin antibiotic containing an unusual hydroxylamino-ether sugar, everhydroxylaminose. Tetrahedron Lett. 2000, 39, 8441–8444. [Google Scholar] [CrossRef]
  63. Chu, M.; Mierzwa, R.; Jenkins, J.; Chan, T.; Das, P.; Pramanik, B.N.; Patel, M.; Gullo, V. Isolation and characterization of novel oligosaccharides related to Ziracin. J. Nat. Prod. 2002, 65, 1588–1593. [Google Scholar] [CrossRef]
  64. Mertz, J.L.; Peloso, J.S.; Barker, B.J.; Babbitt, G.E.; Occolowitz, J.L.; Simson, V.L.; Kline, R.M. Isolation and structural identification of nine avilamycins. J. Antibiot. 1986, 39, 877–887. [Google Scholar] [CrossRef]
  65. Nakashio, S.; Iwasawa, H.; Dun, F.Y.; Kanemitsu, K.; Shimada, J. Everninomicin, a new oligosaccharide antibiotic: Its antimicrobial activity, post-antibiotic effect and synergistic bactericidal activity. Drugs Exp. Clin. Res. 1995, 21, 7–16. [Google Scholar]
  66. Foster, D.R.; Rybak, M.J. Pharmacologic and bacteriologic properties of SCH27899 (Ziracin), an investigational antibiotic from the everninomicin family. Pharmacotherapy 1999, 19, 1111–1117. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  67. Jones, D.J.; Mowrey, D.H.; Anderson, D.B.; Wellenreiter, R.H. Effect of various levels of avilamycin on the performance of growing-finishing swine. J. Anim. Sci. 1987, 65, 881–885. [Google Scholar] [CrossRef] [PubMed]
  68. Shryock, T.R. Will avilamycin convert ziracine into zerocine? Emerg. Infect. Dis. 2001, 7, 488–489. [Google Scholar] [CrossRef]
  69. Arenz, S.; Juette, M.F.; Graf, M.; Nguyen, F.; Huter, P.; Polikanov, Y.S.; Blanchard, S.C.; Wilson, D.N. Structures of the orthosomycin antibiotics avilamycin and evernimicin in complex with the bacterial 70S ribosome. Proc. Natl. Acad. Sci. USA 2016, 113, 7527–7532. [Google Scholar] [CrossRef] [Green Version]
  70. Krupkin, M.; Wekselman, I.; Matzov, D.; Eyal, Z.; Posner, Y.D.; Rozenberg, H.; Zimmerman, E.; Bashan, A.; Yonath, A. Avilamycin and evernimicin induce structural changes in rProteins uL16 and CTC that enhance the inhibition of A-site tRNA binding. Proc. Natl. Acad. Sci. USA 2016, 113, E6796–E6805. [Google Scholar] [CrossRef] [Green Version]
  71. Limbrick, E.M.; Graf, M.; Derewacz, D.K.; Nguyen, F.; Spraggins, J.M.; Wieland, M.; Ynigez-Gutierrez, A.E.; Reisman, B.J.; Zinshteyn, B.; McCulloch, K.M.; et al. Bifunctional nitrone-conjugated secondary metabolite targeting the ribosome. J. Am. Chem. Soc. 2020, 142, 18369–18377. [Google Scholar] [CrossRef] [PubMed]
  72. Gaisser, S.; Trefzer, A.; Stockert, S.; Kirschning, A.; Bechthold, A. Cloning of an avilamycin biosynthetic gene cluster from Streptomyces viridochromogenes Tü57. J. Bacteriol. 1997, 179, 6271–6278. [Google Scholar] [CrossRef] [Green Version]
  73. Weitnauer, G.; Muhlenweg, A.; Trefzer, A.; Hoffmeister, D.; Sussmuth, R.D.; Jung, G.; Welzel, K.; Vente, A.; Girreser, U.; Bechthold, A. Biosynthesis of the orthosomycin antibiotic avilamycin A: Deductions from the molecular analysis of the avi biosynthetic gene cluster of Streptomyces viridochromogenes Tü57 and production of new antibiotics. Chem. Biol. 2001, 8, 569–581. [Google Scholar] [CrossRef] [Green Version]
  74. Weitnauer, G.; Gaisser, S.; Kellenberger, L.; Leadlay, P.F.; Bechthold, A. Analysis of a C-methyltransferase gene (aviG1) involved in avilamycin biosynthesis in Streptomyces viridochromogenes Tü57 and complementation of a Saccharopolyspora erythraea eryBIII mutant by aviG1. Microbiology 2002, 148, 373–379. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  75. Treede, I.; Hauser, G.; Muhlenweg, A.; Hofmann, C.; Schmidt, M.; Weitnauer, G.; Glaser, S.; Bechthold, A. Genes involved in formation and attachment of a two-carbon chain as a component of eurekanate, a branched-chain sugar moiety of avilamycin A. Appl. Environ. Microbiol. 2005, 71, 400–406. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  76. Weitnauer, G.; Hauser, G.; Hofmann, C.; Linder, U.; Boll, R.; Pelz, K.; Glaser, S.J.; Bechthold, A. Novel avilamycin derivatives with improved polarity generated by targeted gene disruption. Chem. Biol. 2004, 11, 1403–1411. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  77. Hofmann, C.; Boll, R.; Heitmann, B.; Hauser, G.; Clemens, D.; Frerich, A.; Weitnauer, G.; Glaser, S.J.; Bechthold, A. Genes encoding enzymes responsible for biosynthesis of L-lyxose and attachment of eurekanate during avilamycin biosynthesis. Chem. Biol. 2005, 12, 1137–1143. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  78. Boll, R.; Hofmann, C.; Heitmann, B.; Hauser, G.; Glaser, S.; Koslowski, T.; Friedrich, T.; Bechthold, A. The active conformation of avilamycin A is conferred by AviX12, a radical AdoMet enzyme. J. Biol. Chem. 2006, 281, 14756–14763. [Google Scholar] [CrossRef] [Green Version]
  79. McCulloch, K.M.; McCranie, E.K.; Smith, J.A.; Sarwar, M.; Mathieu, J.L.; Gitschlag, B.L.; Du, Y.; Bachmann, B.O.; Iverson, T.M. Oxidative cyclizations in orthosomycin biosynthesis expand the known chemistry of an oxygenase superfamily. Proc. Natl. Acad. Sci. USA 2015, 112, 11547–11552. [Google Scholar] [CrossRef] [Green Version]
  80. Weitnauer, G.; Gaisser, S.; Trefzer, A.; Stockert, S.; Westrich, L.; Quiros, L.M.; Mendez, C.; Salas, J.A.; Bechthold, A. An ATP-binding cassette transporter and two rRNA methyltransferases are involved in resistance to avilamycin in the producer organism Streptomyces viridochromogenes Tü57. Antimicrob. Agents Chemother. 2001, 45, 690–695. [Google Scholar] [CrossRef] [Green Version]
  81. Rebets, Y.; Boll, R.J.; Horbal, L.; Fedorenko, V.; Bechthold, A. Production of avilamycin A is regulated by AviC1and AviC2, two transcriptional activators. J. Antibiot. 2009, 62, 461–464. [Google Scholar] [CrossRef] [Green Version]
  82. Limbrick, E.M.; Ynigez-Gutierrez, A.E.; Dulin, C.C.; Derewacz, D.K.; Spraggins, J.M.; McCulloch, K.M.; Iverson, T.M.; Bachmann, B.O. Methyltransferase contingencies in the pathway of everninomicin D antibiotics and analogues. ChemBioChem 2020, 21, 3349–3358. [Google Scholar] [CrossRef] [PubMed]
Marinedrugs 19 00350 g001 550
Figure 1. The chemical structures of compounds 1–12.
Figure 1. The chemical structures of compounds 1–12.
Marinedrugs 19 00350 g001
Marinedrugs 19 00350 g002 550
Figure 2. The chemical structures of compounds 13–24.
Figure 2. The chemical structures of compounds 13–24.
Marinedrugs 19 00350 g002
Marinedrugs 19 00350 g003 550
Figure 3. The chemical structures of compounds 25–39.
Figure 3. The chemical structures of compounds 25–39.
Marinedrugs 19 00350 g003
Marinedrugs 19 00350 g004a 550Marinedrugs 19 00350 g004b 550
Figure 4. The gene cluster and biosynthesis of acarbose and acarviostatins. (A) Comparison between acarbose biosynthetic gene cluster (acb-cluster) of Actinoplanes sp. SE50/110 and acarviostatin biosynthetic gene cluster (sct-cluster) of Streptomyces coelicoflavus ZG0656. The functions of eight genes in the acb-cluster (AcbA, AcbB, AcbV, AcbC, AcbM, AcbO, AcbL, and AcbN) are experimentally defined by proteomic studies, while the functions of the remaining genes in acb-cluster and all genes in the sct-cluster are proposed by bioinformatic analyses. (B) The proposed intracellular biosynthetic pathway of acarbose in Actinoplanes sp. SE50/110 and acarviostatin in Streptomyces coelicoflavus ZG0656. (C) The proposed extracellular biosynthesis of acarviostatins and the carbophor in Streptomyces coelicoflavus ZG0656.
Figure 4. The gene cluster and biosynthesis of acarbose and acarviostatins. (A) Comparison between acarbose biosynthetic gene cluster (acb-cluster) of Actinoplanes sp. SE50/110 and acarviostatin biosynthetic gene cluster (sct-cluster) of Streptomyces coelicoflavus ZG0656. The functions of eight genes in the acb-cluster (AcbA, AcbB, AcbV, AcbC, AcbM, AcbO, AcbL, and AcbN) are experimentally defined by proteomic studies, while the functions of the remaining genes in acb-cluster and all genes in the sct-cluster are proposed by bioinformatic analyses. (B) The proposed intracellular biosynthetic pathway of acarbose in Actinoplanes sp. SE50/110 and acarviostatin in Streptomyces coelicoflavus ZG0656. (C) The proposed extracellular biosynthesis of acarviostatins and the carbophor in Streptomyces coelicoflavus ZG0656.
Marinedrugs 19 00350 g004aMarinedrugs 19 00350 g004b
Marinedrugs 19 00350 g005 550
Figure 5. The chemical structures of saccharomicins A and B (40 and 41). Agl: aglycone; sFuc: sulfated fucose; Sac: saccharosamine; Fuc: fucose; Rha: rhamnose; Eva: 4-epi-vancosamine; Dig: digitoxose.
Figure 5. The chemical structures of saccharomicins A and B (40 and 41). Agl: aglycone; sFuc: sulfated fucose; Sac: saccharosamine; Fuc: fucose; Rha: rhamnose; Eva: 4-epi-vancosamine; Dig: digitoxose.
Marinedrugs 19 00350 g005
Marinedrugs 19 00350 g006 550
Figure 6. The gene cluster and biosynthesis of saccharomicin A. (A) The biosynthetic gene cluster of saccharomicin A. The functions of twelve genes in the saccharomicin A biosynthetic gene cluster (Sam5, Sam8, and Sam11-20) are experimentally defined by proteomic studies, while the functions of the remaining genes are proposed by bioinformatic analyses. (B) Biosynthetic pathway of the saccharomicin aglycone. (C) The proposed glycosylation pathway in saccharomicin A biosynthesis.
Figure 6. The gene cluster and biosynthesis of saccharomicin A. (A) The biosynthetic gene cluster of saccharomicin A. The functions of twelve genes in the saccharomicin A biosynthetic gene cluster (Sam5, Sam8, and Sam11-20) are experimentally defined by proteomic studies, while the functions of the remaining genes are proposed by bioinformatic analyses. (B) Biosynthetic pathway of the saccharomicin aglycone. (C) The proposed glycosylation pathway in saccharomicin A biosynthesis.
Marinedrugs 19 00350 g006
Marinedrugs 19 00350 g007 550
Figure 7. The chemical structure of hygromycin B (42).
Figure 7. The chemical structure of hygromycin B (42).
Marinedrugs 19 00350 g007
Marinedrugs 19 00350 g008 550
Figure 8. The chemical structures of compounds 43–62. Two orthoester linkages were marked with a red line, while the methylenedioxy bridge was marked with a blue line.
Figure 8. The chemical structures of compounds 43–62. Two orthoester linkages were marked with a red line, while the methylenedioxy bridge was marked with a blue line.
Marinedrugs 19 00350 g008
Marinedrugs 19 00350 g009 550
Figure 9. The chemical structures of compounds 63–99. Two orthoester linkages were marked with a red line, while the methylenedioxy bridge was marked with a blue line.
Figure 9. The chemical structures of compounds 63–99. Two orthoester linkages were marked with a red line, while the methylenedioxy bridge was marked with a blue line.
Marinedrugs 19 00350 g009
Marinedrugs 19 00350 g010 550
Figure 10. The proposed Avi A biosynthetic pathway (the blue branch is for dichloroisoeverninic acid (moiety A), the orange one is for d-olivose (residues B and C) and 2-deoxy-d-evalose (residue D), the pink branch is for d-fucose (residue E) and methyleurekanate (residue H), while the green one is for d-mannose (residue F) and l-lyxose (residue G); the content in the square bracket represents the published year of genes. The genes in the Avi A biosynthetic gene cluster mentioned above are experimentally defined by proteomic studies.
Figure 10. The proposed Avi A biosynthetic pathway (the blue branch is for dichloroisoeverninic acid (moiety A), the orange one is for d-olivose (residues B and C) and 2-deoxy-d-evalose (residue D), the pink branch is for d-fucose (residue E) and methyleurekanate (residue H), while the green one is for d-mannose (residue F) and l-lyxose (residue G); the content in the square bracket represents the published year of genes. The genes in the Avi A biosynthetic gene cluster mentioned above are experimentally defined by proteomic studies.
Marinedrugs 19 00350 g010
Table
Table 1. The deduced functions of the acarviostatins biosynthetic genes in S. coelicoflavus ZG0656.
Table 1. The deduced functions of the acarviostatins biosynthetic genes in S. coelicoflavus ZG0656.
GenesAmino AcidsIdentity/Similarity to the acb-ClusterProposed Function
SctZ2161950%/63% homologous to AcbZα-amylase
SctZ1104247%/59% homologous to AcbZα-amylase
SctE256525%/39% homologous to AcbDα-amylase
SctC2352no homologueLacI family transcriptional regulator
SctE155325%/36% homologous to AcbEα-glucosidase
SctG30126%/51% homologous to AcbGABC transporter membrane protein
SctF33529%/50% homologous to AcbFABC transporter membrane protein
SctH42425%/37% homologous to AcbHABC transporter membrane protein
SctC1342no homologuemalR-like regulator
SctB32559%/70% homologous to AcbBdTDP-glucose 4,6-dehydratase
SctA35743%/59% homologous to AcbAdTDP-glucose synthase
SctV41775%/83% homologous to AcbVdTDP-4-keto-6-deoxy-glucose 4-aminotransferase
SctW34162%/77% homologous to AcbWABC transporter permease protein
SctX27449%/68% homologous to AcbXABC transporter permease protein
SctY26857%/75% homologous to AcbYABC transporter permease protein
SctU48742%/51% homologous to AcbU1-epi-valienol-7-phosphate-1-kinase
SctS69162%/71% homologous to AcbSglycosyltransferase
SctR35470%/80% homologous to AcbR1-epi-valienol-1,7-bisphosphate-1-adenylyltransferase
SctK30848%/60% homologous to AcbKacarbose-7-kinase
SctI102747%/59% homologous to AcbIputative glycosyltransferase
SctQ70255%/66% homologous to AcbQputative acarbose 4-alpha-glucanotransferase
SctC39339%/52% homologous to AcbC2-epi-5-epi-valiolone synthase
SctJ138no homologue2-epimerase
SctM35031%/43% homologous to AcbMC7-cyclitol-7-kinase
SctO324no homologueputative 2-epi-5-epi-valiolone dehydratase
SctT464no homologueunknown
Scim112no homologueα-amylase
Table
Table 2. The proposed functions of the AVI biosynthetic genes in S. viridochromogenes Tü57.
Table 2. The proposed functions of the AVI biosynthetic genes in S. viridochromogenes Tü57.
Genes Encoded EnzymesProposed Function
avi Nketoacyl synthase III homologues controlling the starter unit for orstainic acid biosynthesis
avi Mtype I polyketide synthaseorstainic acid biosynthesis
avi DdTDP-glucose synthasestarter enzyme for residues B, C, D biosynthesis
avi E1, aviSdTDP-glucose-4,6-dehydrataseresidues B, C, D biosynthesis
avi E2UDP-glucuronic acid decarboxylasestarter enzyme for residue G biosynthesis
avi E3GDP-mannose-4,6-dehydratasestarter enzyme for residue E biosynthesis
avi B1, avi B2pyruvate dehydrogenase (α2β2 chains)residue H biosynthesis
avi G1C-methyltransferaseresidue D biosynthesis
avi G5O-methyltransferaseC-4 methylation of residue E
avi G2, avi G6O-methyltransferaseC-2, C-6 methylation of residue F
avi G3O-methyltransferaseresidue H methylation
avi G4O-methyltransferaseresidue N methylation
avi Q1-avi Q3UDP-glucose-4-epimeraseepimerization of oligosaccharides
avi Z1ketoreductaseresidues D and E synthesis
avi Tketoreductaseresidues B-D synthesis
avi Z3ketoreductaseresidues B and C synthesis
avi Z2ketoreductaseresidues D and E synthesis
avi Hhalogenasehalogenated residue A
avi X12S-adenosylmethioninaseactivated residues F and G
avi O1, avi O3hydroxylaseformation of orthoester bond and glycosidic bond
Avi O2hydroxylaseresidue H biosynthesis
avi GT1-avi GT3glycosyltransferaseassembly of heptasaccharide chain
avi GT4glycosyltransferaseconjugation between residues G and H
avi C1, avi C2regulatorAVI positive regulator
avi Ra, avi RbrRNA methyltransferaseAVI resistance
avi ABC1, avi ABC2ABC transporter, ATP binding proteinAVI antibiotic transport
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Share and Cite

MDPI and ACS Style

Xu, J.-L.; Liu, Z.-F.; Zhang, X.-W.; Liu, H.-L.; Wang, Y. Microbial Oligosaccharides with Biomedical Applications. Mar. Drugs 2021, 19, 350. https://doi.org/10.3390/md19060350

AMA Style

Xu J-L, Liu Z-F, Zhang X-W, Liu H-L, Wang Y. Microbial Oligosaccharides with Biomedical Applications. Marine Drugs. 2021; 19(6):350. https://doi.org/10.3390/md19060350

Chicago/Turabian Style

Xu, Jian-Lin, Zhi-Feng Liu, Xiao-Wei Zhang, Hai-Li Liu, and Yong Wang. 2021. "Microbial Oligosaccharides with Biomedical Applications" Marine Drugs 19, no. 6: 350. https://doi.org/10.3390/md19060350

APA Style

Xu, J. -L., Liu, Z. -F., Zhang, X. -W., Liu, H. -L., & Wang, Y. (2021). Microbial Oligosaccharides with Biomedical Applications. Marine Drugs, 19(6), 350. https://doi.org/10.3390/md19060350

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop