|Transcriptional and functional characterization of genetic elements involved in galacto-oligosaccharide utilization by Bifidobacterium breve UCC2003.|
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|PMID: 23199239 Owner: NLM Status: MEDLINE|
|Several prebiotics, such as inulin, fructo-oligosaccharides and galacto-oligosaccharides, are widely used commercially in foods and there is convincing evidence, in particular for galacto-oligosaccharides, that prebiotics can modulate the microbiota and promote bifidobacterial growth in the intestinal tract of infants and adults. In this study we describe the identification and functional characterization of the genetic loci responsible for the transport and metabolism of purified galacto-oligosaccharides (PGOS) by Bifidobacterium breve UCC2003. We further demonstrate that an extracellular endogalactanase specified by several B. breve strains, including B. breve UCC2003, is essential for partial degradation of PGOS components with a high degree of polymerization. These partially hydrolysed PGOS components are presumed to be transported into the bifidobacterial cell via various ABC transport systems and sugar permeases where they are further degraded to galactose and glucose monomers that feed into the bifid shunt. This work significantly advances our molecular understanding of bifidobacterial PGOS metabolism and its associated genetic machinery to utilize this prebiotic.|
|Mary O'Connell Motherway; Michael Kinsella; Gerald F Fitzgerald; Douwe van Sinderen|
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|Type: Journal Article; Research Support, Non-U.S. Gov't Date: 2012-12-02|
|Title: Microbial biotechnology Volume: 6 ISSN: 1751-7915 ISO Abbreviation: Microb Biotechnol Publication Date: 2013 Jan|
|Created Date: 2012-12-20 Completed Date: 2013-06-12 Revised Date: 2014-02-14|
Medline Journal Info:
|Nlm Unique ID: 101316335 Medline TA: Microb Biotechnol Country: United States|
|Languages: eng Pagination: 67-79 Citation Subset: IM|
|© 2012 The Authors. Published by Society for Applied Microbiology and Blackwell Publishing Ltd. This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.|
|APA/MLA Format Download EndNote Download BibTex|
ATP-Binding Cassette Transporters
Bacterial Proteins / genetics, metabolism
Bifidobacterium / classification, enzymology, genetics*, metabolism*
Galactose / metabolism*
Membrane Transport Proteins / genetics, metabolism*
Oligosaccharides / metabolism*
beta-Galactosidase / genetics, metabolism*
|0/Bacterial Proteins; 0/Membrane Transport Proteins; 0/Oligosaccharides; 0/Prebiotics; EC 184.108.40.206/beta-Galactosidase; X2RN3Q8DNE/Galactose|
Journal ID (nlm-ta): Microb Biotechnol
Journal ID (iso-abbrev): Microb Biotechnol
Journal ID (publisher-id): mbt
Publisher: Blackwell Publishing Ltd
Journal compilation © 2013 Society for Applied Microbiology and Blackwell Publishing Ltd
Received Day: 25 Month: 5 Year: 2012
Revision Received Day: 03 Month: 10 Year: 2012
Accepted Day: 24 Month: 10 Year: 2012
Print publication date: Month: 1 Year: 2013
Electronic publication date: Day: 02 Month: 12 Year: 2012
Volume: 6 Issue: 1
First Page: 67 Last Page: 79
PubMed Id: 23199239
|Transcriptional and functional characterization of genetic elements involved in galacto-oligosaccharide utilization by Bifidobacterium breve UCC2003|
|Mary O'Connell Motherway12|
|Gerald F Fitzgerald123|
1Alimentary Pharmabiotic Centre, National University of IrelandWestern Road, Cork, Ireland
2Departments of Microbiology, National University of IrelandWestern Road, Cork, Ireland
3Food and Nutritional Sciences, National University of IrelandWestern Road, Cork, Ireland
|Correspondence: *For correspondence. E-mail firstname.lastname@example.org; Tel. 00 353 21 490 1365; Fax 00 353 21 490 3101.
Funding Information The Alimentary Pharmabiotic Centre is a research centre funded by Science Foundation Ireland (SFI), through the Irish Government's National Development Plan. The authors and their work were supported by SFI (Grant Nos 02/CE/B124 and 07/CE/B1368) and a HRB postdoctoral fellowship (Grant No. PDTM/20011/9) awarded to MOCM. The Mass Spectroscopy Instrument and analysis was funded under the Higher Education Authority Programme for Research in Third-Level Institutions (PRTLI) and co-funded under the European Regional Development Fund.
Neonates possess an immature intestinal immune system, a gastrointestinal tract devoid of a microbiota and a stomach with a relatively high pH, which is not effective in eliminating pathogens, thereby making newborns highly susceptible to infection. Colonization of the human gut commences at birth, when the mother's vaginal and faecal microbiota are considered to be the most important inocula (Vaishampayan et al., 2010). It has furthermore been suggested that mother's milk serves as an inoculum for breastfeeding infants as bacteria from the maternal gut are believed to reach the mammary gland through an endogenous route, the so-called ‘entero-mammary pathway’ that involves maternal dendritic cells and macrophages (Martín et al., 2003; Perez et al., 2007). Evidence is accumulating on the importance of the human gut microbiota in educating the immune system at this very early stage of extrauterine life (Martín et al., 2010). There is a broad consensus that breastfeeding is the best option for optimal development of the infant's intestinal microbiota, so as to promote a healthy, balanced immune system (reviewed by Marques et al., 2010). Human milk is a functional food; it contains semi-essential nutrients, free amino acids, enzymes, hormones, growth factors, polyamines, nucleotides and oligosaccharides (Walker, 2007b). Research has indicated that human milk has a protective effect against diarrhoeal diseases, respiratory tract infections, bacteremia, meningitis and necrotizing enterocolitis, all presumed to be mediated through its bioactive components (Martín et al., 2010). Human milk oligosaccharides (HMOs) are the main prebiotic factors in human milk and, while they do not directly nourish infants, HMOs are thought to enrich for specific gut commensals capable of utilizing these diverse substrates, in particular bifidobacteria that are abundant in and characteristic of the breastfed baby's intestinal microbiota (Sela and Mills, 2010; Sela, 2011).
Bifidobacteria are anaerobic, saccharolytic, high GC-content, Gram-positive bacteria that are non-motile and do not sporulate or produce gas through their fermentative metabolism (reviewed by Turroni et al., 2011). Bifidobacteria are frequently reported as being numerically dominant in the faecal microbiota of breastfed infants while their numbers decline on weaning and thereafter resemble those of the adult microbiota. The many beneficial effects associated with a breastfed infant microbiota, being high in bifidobacterial numbers, has resulted in major efforts being directed at manipulating infant food formulations so as to achieve in bottle-fed infants an intestinal microbiota composition resembling that found in breastfed babies. HMOs are very diverse in composition and structure (Niñonuevo et al., 2006; Lo Cascio et al., 2009; Niñonuevo and Lebrilla, 2009; Nwosu et al., 2012) and as yet these are not available for incorporation into infant food formulations. Consequently research has focused on the development of alternative prebiotic, non-human milk-derived oligosaccharides, such as galacto-oligosaccharides (GOS).
GOS are non-digestible oligosaccharides that are produced by enzymatic transglycosylation of lactose using β-galactosidases, thereby generating a mixture of oligomers of varying chain length ranging from DP2 to DP15 (Barboza et al., 2009). The raw material for the production of GOS is whey-derived lactose which is a by-product of the dairy industry. The composition of GOS is dependent on the source of the enzyme, substrate concentration and pH, furthermore, since GOS production involves a transglycosylation process which competes with the hydrolytic activity of the enzymes, GOS always contain a significant amount of lactose as well as its constituent monosaccharides galactose and glucose (Coulier et al., 2009).
Since 2002, several infant formulations containing specific mixtures of short-chain GOS (scGOS) and long-chain fructo-oligosaccharides (lcFOS) have been on the market. These formulations have been designed to elicit a prebiotic/bifidogenic effect comparable to that of human milk, as demonstrated in numerous clinical trials (reviewed by MacFarlane and Macfarlane, 2007; Sangwan et al., 2011). Furthermore, there is an increasing body of evidence that prebiotic supplementation of food formulations with GOS provides protection against pathogen infection (Eversbach et al., 2010; Searle et al., 2010; Quintero et al., 2011).
To date several β-galactosidases of bifidobacterial origin have been described in the literature and much research has focused on the ability of these enzymes to hydrolyse and synthesize GOS (Van Laere et al., 2000; Barboza et al., 2009; Goulas et al., 2009; Osman et al., 2010; 2012). In the present study we evaluated the transcriptional response of the human (infant) gut commensal Bifidobacterium breve UCC2003 during growth on a purified Vivinal® GOS (PGOS) formulation that contains very low levels of monosaccharides and lactose. Our results indicate that PGOS metabolism by B. breve UCC2003 is the result of the concerted action of several β-galactosidases and their associated transport systems that internalize GOS components. We furthermore demonstrate that an extracellular endogalactanase specified by several B. breve strains, including B. breve UCC2003, is essential for metabolism of GOS components with a long retention time and high degree of polymerization. The resulting endogalactanase-mediated breakdown products are transported into the bifidobacterial cell via various ABC transport systems and permeases where they are further metabolized to galactose and glucose, the latter feeding directly into the so-called bifid shunt, while the former likely being channelled through the Leloir pathway and converted to glucose 6-phosphate before entering the bifid shunt.
We previously established that not all B. breve strains possess endogalactanase activity and by comparative genome hybridization were able to establish that the presence of endogalactanase activity is strictly correlated with the presence of the galA gene in the B. breve strains examined (O'Connell Motherway et al., 2011b). In order to investigate the importance of endogalactanase activity for PGOS metabolism, growth of 13 B. breve strains, namely UCC2003, UCC2005, JCM7017, JCM7019, NCFB2257, NCFB2258, NCIMB8815, NCIMB11815, LMG13208, NIZO658, UCC2008, UCC2009 and UCC2010, was profiled in Modified Rogosa with 0.5% lactose or PGOS as the sole carbohydrate source. All strains grew well on lactose reaching an OD 600nm ≥ 1.0 within 8 h of growth, while growth on PGOS separated the B. breve strains into two groups: the first group all grew well on PGOS reaching an OD 600nm ≥ 1.0 within 9 h of growth while for the second group a final OD 600nm of ≤ 1.0 was achieved in the 24 h of the growth profile (Fig. 1). These two distinct bifidobacterial growth profiles correlated with the endogalactanase-positive (GalA+) and endogalactanase-negative (GalA−) strains respectively. Post-fermentation, cell-free supernatants were analysed by HPAEC-PAD and demonstrated that the GalA+B. breve strains utilized almost all of the GOS components (Fig. 2A), while the GalA− strains exhibited more variability in the GOS fractions that were metabolized. The GalA− strains did not utilize PGOS components with a long retention time (between 30 and 48 min), which represent galacto-oligosaccharides with a high degree of polymerization (DP) (Coulier et al., 2009) (Fig. 2B), indicating that GalA is responsible for the extracellular degradation of these high DP GOS components.
In order to investigate which genes may be involved in PGOS metabolism in B. breve UCC2003, global gene expression was determined by microarray analysis during growth of this bifidobacterial strain on PGOS and this was compared with its expression pattern when grown on ribose as sole carbohydrate source. Total RNA was isolated from mid-log phase cultures of B. breve UCC2003 grown on PGOS or ribose as the sole carbohydrate source. Analysis of the DNA microarray data revealed that the expression of four gene clusters was significantly upregulated when UCC2003 was grown on PGOS (fold change > 3.0, P < 0.001; Table 1 and Fig. 3). The first GOS-inducible cluster of six genes, galC, galD, galE galG, galR and galA, constitute the previously identified galactan metabolism cluster (O'Connell Motherway et al., 2011b), while the second cluster, Bbr_1551 to Bbr_1553, consists of three genes specifying a predicted galactoside symporter and a GH2 family β-galactosidase in divergent orientations, designated here as lacS and lacZ respectively, and an associated gene encoding a putative LacI-type transcriptional regulator. The third GOS-inducible cluster comprises five genes, Bbr_0526 to Bbr_530, that are predicted to specify a LacI-type transcriptional regulator, two ABC-type permeases, a GH42 family β-galactosidase and a solute-binding protein, which are designated gosR, gosD, gosE gosG and gosC respectively. The fourth set of upregulated genes are the presumed galT and galK genes that encode Galactose-1-phosphate uridyltransferase and galactokinase respectively (Kitaoka et al., 2005; Fushinobu, 2010), and represent key enzymes of the Leloir pathway that converts galactose to D-glucose 6-phosphate that can feed into the bifid shunt (Fushinobu, 2010; Pokusaeva et al., 2011a) (Fig. 3).
In order to determine how disruption of particular genes from the galCDEGR, lacSZI and gosRDEGC gene clusters would impact on the ability of B. breve UCC2003 to metabolize PGOS, the previously constructed mutant strains B. breve UCC2003-galA, UCC2003-galC and UCC2003-galG were employed (O'Connell Motherway et al., 2011b). Additional insertion mutants in the B. breve lacS, lacZ, gosD and gosG genes were generated, resulting in strains B. breve UCC2003-lacS, UCC2003-lacZ, UCC2003-gosD and UCC2003-gosG respectively (Table 2). To determine the components of PGOS that were metabolized by each of these insertion mutants as compared with B. breve UCC2003, strains UCC2003 (wild type), and these seven insertion mutant strains were analysed for their ability to grow in mMRS supplemented with PGOS, lactose, lactulose or ribose (positive control) as the sole carbon source and the cell-free, post-fermentation supernatants of PGOS fermentation were analysed for remaining PGOS fractions by HPAEC-PAD. As expected, and in contrast to the wild-type, the B. breve UCC2003-lacS insertion mutant was shown to be incapable of growth on lactose (Fig. 4AII) or lactulose (results not shown) as the sole carbon source thereby identifying LacS as the main lactose/lactulose transporter in this strain. Intriguingly, B. breve UCC2003-lacZ is capable of growth on lactose (Fig. 4AII) and lactulose (results not shown) as the sole carbohydrate source provided. This growth could be attributed to the presence of one or more additional β-galactosidases that can hydrolyse lactose in the absence of functional LacZ. Candidates for such alternative β-galactosidase-encoding genes are lacZ2, which is predicted to encode a GH2 family β,1-4-galactosidase, gosG or galG (O'Connell Motherway et al., 2011b). To test this possibility these four prospective β-galactosidases, LacZ2, GosG, GalG and LacZ, were expressed in Lactococcus lactis NZ9000 using the nisin-inducible expression system (de Ruyter et al., 1996) after which β-galactosidase activity was measured in cell lysates of the various strains. Following nisin induction, cells of L. lactis NZ9000 expressing each of the four predicted bifidobacterial β-galactosidases exhibited significantly increased β-galactosidase activity thereby demonstrating that LacZ2, GosG, GalG and LacZ, can indeed hydrolyse lactose (Fig. 4B). The observed growth of the UCC2003-lacZ mutant strain in mMRS supplemented with lactose as the sole carbohydrate source is therefore likely due to the activity of one or more of the β-galactosidase enzymes specified by lacZ2, gosG or galG.
When growth was examined using PGOS as the sole carbohydrate source, B. breve UCC2003-galA, B. breve UCC2003-galC and B. breve UCC2003-galG reached lower final optical densities as compared with UCC2003 or indeed the other four insertion mutant strains (Fig. 4AIII). These data suggest key roles for the endogalactanase encoded by galA, the ABC transport system specified by galCDE and the β-galactosidase encoded by galG in the metabolism of PGOS by B. breve UCC2003.
HPAEC-PAD analysis of the cell-free supernatants identified that the B. breve UCC2003-galA strain did not metabolize PGOS components with a predicted high degree of polymerization (retention time 30–48 min) (Fig. 5C). This finding was verified by Mass Spectroscopy analysis that demonstrated that B. breve UCC2003 consumed all detectable PGOS fractions, while B. breve UCC2003-galA could only metabolize PGOS fractions with a DP of up to and equal to three (Fig. 6). Interestingly, a GOS component present in fractions eluted from 22.5 to 25 min, of the HPAEC analysis, was shown to increase in the CFS of B. breve UCC2003-galC (Fig. 5D). This GOS component is likely β,1-4 linked galactotriose, which is the main product of the endogalactanase activity (Hinz et al., 2005; O'Connell Motherway et al., 2011b), and which is apparently not transported by this strain due to the galC mutation. When B. breve UCC2003-lacS was grown on PGOS, it was incapable of internalizing lactose, a GalA-mediated PGOS degradation product, which therefore accumulates in the growth medium, and which elutes at approximately 14 min under the conditions tested (Fig. 5F). The CFS post-fermentation profiles obtained following growth of UCC2003-galG (Fig. 5E), UCC2003-lacZ (Fig. 5G), or UCC2003-gosG (Fig. 5I) in PGOS-containing medium, closely resembled that of B. breve UCC2003, a result that was not unexpected given that GalG, LacZ and GosG are all intracellular β-galactosidases, while the extracellular endogalactanase activity and transport functions are fully functional in these mutant strains.
To demonstrate that the protein product of galA is uniquely necessary for the metabolism of galacto-oligosaccharides with a DP > 3, two complementation experiments were performed. In the first, the endogalactanase-encoding gene, galA, was cloned under the control of its own promoter on plasmid pBC1.2 and introduced into B. breve UCC2003-galA (to generate strain UCC2003-galA-pBC1.2-galA; see Experimental procedures). Expression of GalA in strain UCC2003-galA-pBC1.2-galA allowed this strain to grow on PGOS to an optical density comparable to B. breve UCC2003 (Fig. 7Aii), while HPAEC analysis of the post-fermentation CFS of UCC2003-galA-pBC1.2-galA clearly shows the consumption of the PGOS fractions with a high degree of polymerization (Fig. S1). For the second complementation experiment plasmid pBC1.2-galA was introduced into the GalA− strain B. breve NCFB2257 (to generate strain B. breve NCFB2257-pBC1.2-galA). Expression of GalA in B. breve NCFB2257-pBC1.2-galA enabled this strain to grow to a higher optical density compared with the wild type, B. breve NCFB2257, when grown on PGOS as the sole carbohydrate source. This PGOS-dependent growth profile of B. breve NCFB2257-pBC1.2-galA was comparable to those observed for GalA+B. breve strains (Fig. 7B), while HPAEC analysis demonstrated that B. breve NCFB2257-pBC1.2-galA could metabolize PGOS components with a high degree of polymerization (Fig. S2). These complementation experiments unequivocally demonstrate the role of GalA in the metabolism of PGOS with a high degree of polymerization and long retention time.
Several studies have demonstrated that bifidobacteria dedicate a significant portion of their coding capacity to the metabolism of a wide variety of carbohydrates (Schell et al., 2002; Ventura et al., 2007a,b). Over 50 different bifidobacterial carbohydrases have been described in the literature to date (reviewed by Van den Broek et al., 2008; Pokusaeva et al., 2011a). Using B. breve UCC2003 as a model to study bifidobacterial carbohydrate metabolism, we previously characterized an operon encoding a β-fructofuranosidase (Ryan et al., 2005), an extracellular amylopullulanase which hydrolyses α-1,4 and α-1,6 glucosidic linkages in starch and related polysaccharides (Ryan et al., 2006; O'Connell Motherway et al., 2012), two α-glucosidases exhibiting hydrolytic activities towards panose, isomaltose, isomaltotriose and four sucrose isomers-palatinose, trehalulose, turanose and maltulose (Pokusaeva et al., 2009), as well as gene clusters dedicated to ribose (Pokusaeva et al., 2010), galactan (O'Connell Motherway et al., 2011b) and cellodextrin (Pokusaeva et al., 2011b) metabolism. In addition, a PEP-PTS system involved in fructose metabolism was identified and studied in this bacterium (Maze et al., 2007).
In this study, we describe the identification and functional characterization of genetic loci involved in the utilization of PGOS by B. breve UCC2003. To date several studies have demonstrated the presence of β-galactosidase isoenzymes in bifidobacteria (Van Laere et al., 2000; Barboza et al., 2009; Goulas et al., 2009; Osman et al., 2010); however, to our knowledge this is the first study adopting functional genomics approaches to understand the apparent synergistic relationship between β-galactosidases and their associated transport systems required for PGOS metabolism by bifidobacteria.
A range of B. breve strains was tested for their ability to grow on PGOS as the sole carbohydrate source, and while all strains were shown to grow well on PGOS, reaching final optical densities of ≥ 0.8, two distinct groups could be identified based on the growth profiles and analysis of the post-fermentation cell-free supernatants by HPAEC-PAD. The first group included B. breve UCC2003 and for this group HPAEC-PAD analysis showed that all strains metabolized most GOS components including those with a high degree of polymerization. Interestingly and consistent with our expectations, CGH analysis (O'Connell Motherway et al., 2011a) revealed that these strains each encoded an extracellular endogalactanase. The strains in the second group also grew well on PGOS but reached a lower final optical density; however, HPAEC-PAD analysis of the post-fermentation CFS clearly showed that oligosaccharides with a high degree of polymerization remained in the CFS of these strains and were not metabolized. This correlated with the CGH analysis where each of these strains was found to lack the galA gene. These data suggest a key role for GalA in the metabolism of galacto-oligosaccharides with a high degree of polymerization.
DNA microarrays that allowed comparison of gene expression of exponentially growing B. breve UCC2003 when grown on either PGOS or ribose as the sole carbohydrate source identified four gene clusters that are highly upregulated. These include the previously described galactan gene cluster, galBCDEGRA (O'Connell Motherway et al., 2011b), as well as three additional clusters gosRDEGC, lacSZI and galTK. Here we demonstrate that compared with the parent strain UCC2003, the galA, galC and galG mutant strains exhibited impaired growth on PGOS, thereby demonstrating that the endogalactanase, ABC transport system and β-galactosidase encoded by the gal locus significantly contribute to the extracellular metabolism, transport and subsequent intracellular metabolism of PGOS oligosaccharides respectively. Furthermore, analysis of the CFS of UCC2003-galA by HPAEC-PAD following growth on PGOS identified the presence of oligosaccharide fractions with a high degree of polymerization as observed for the galA−B. breve strains and further supporting the importance of GalA in the metabolism of GOS oligosaccharide fractions with a high degree of polymerization. Our recent studies on starch (O'Connell Motherway et al., 2012) and cellodextrin (Pokusaeva et al., 2011b) metabolism by B. breve UCC2003 have demonstrated that the associated ABC transport systems can internalize malto-oligosaccharides or cellodextrins with a DP of 2–5. We would therefore expect that the B. breve gal and gos locus encoded ABC transport systems would transport PGOS fractions with similar relatively low degrees of polymerization and that utilization of GOS oligosaccharide fractions with a high degree of polymerization requires initial extracellular degradation by endogalactanase. This expectation was confirmed by Mass Spectroscopy analysis which demonstrated that GalA enables bifidobacterial cells to metabolize PGOS components with a DP ≥ 4. It is plausible that other Bifidobacterium sp. may possess an extracellular β-galactosidase that may fulfil a similar role; however, to date just two extracellular β-galactosidases from bifidobacteria have been described in the literature: while Moller and colleagues (2001) did not evaluate the ability of the extracellular β-galactosidase, BIF3, from B. bifidum DSM20215 to hydrolyse GOS, BbgIII from B. bifidum NCIMB41171 was found to have a high affinity for lactose hydrolysis but exhibited relatively low GOS hydrolysis activity (Goulas et al., 2009).
Our results also demonstrate a significant role for the LacS symporter in transporting lactose, lactulose and possibly other GOS di-/oligo-saccharides into B. breve UCC2003. Collectively these data demonstrate that PGOS metabolism by B. breve UCC2003 can be attributed to the cooperative activity of multiple β-galactosidases and their associated transport systems. Our observations are consistent with those of Barboza and colleagues (2009) who examined PGOS consumption of four bifidobacterial strains, namely B. breve ATCC15700, B. longum subsp. infantis ATCC15697, B. adolescentis DSM20083 and B. longum subsp. longum DJ010A, and observed strain specific preferences for PGOS utilization. Interestingly, and in contrast to our findings for B. breve UUCC2003, Andersen and colleagues (2011) have recently reported that LacS is the sole transporter of lactose, lactulose, lactitol and GOS into Lactobacillus acidophilus NCFM although it has yet to be demonstrated if L. acidophilus NCFM can utilize GOS components with a high degree of polymerization.
The ability of probiotic strains to ferment particular oligo- and poly-saccharides has been the basis for their selection as prebiotics and incorporation into functional foods. The health benefits associated with GOS are well documented and many placebo controlled clinical trials have explored the health benefits of incorporating GOS in functional food formulations. It is now well documented that GOS promotes the proliferation of beneficial bacteria, in particular bifidobacteria, in the gut, which can subsequently provide protection against colonization with pathogens thereby reducing the incidence of infections. In addition, metabolism of GOS by the gut microbiota leads to the production of short-chain fatty acids (SCFAs). These SCFAs are reported to have numerous beneficial health effects that include reducing cancer risk, increased mineral absorption, improving bowel habit, stool consistency and reduction of IBD inflammation (Davis et al., 2011 reviewed by MacFarlane et al., 2008; Sangwan et al., 2011).
Future research will focus on characterizing the specific PGOS components that are metabolized by B. breve UCC2003, in particular identifying the PGOS structures that are metabolized by GalA, identifying the GOS components that are transported by the ABC-transport systems and LacS. It will also be necessary to determine if differences exist in substrate specificities of the identified β-galactosidases. The results presented here significantly advance our knowledge of GOS metabolism by bifidobacteria and, in due course, may contribute towards the development of targeted bifidogenic galacto-oligosaccharides, for specific probiotic strains. The incorporation of such galacto-oligosaccharides in foods has potential for the development of enhanced functional foods or infant food formulas.
The description of the Experimental procedures resides in Appendix S1 in Supporting information.
The authors wish to acknowledge FrieslandCampina for the gift of Purified GOS. The Alimentary Pharmabiotic Centre is a research centre funded by Science Foundation Ireland (SFI), through the Irish Government's National Development Plan. The authors and their work were supported by SFI (Grant Nos 02/CE/B124 and 07/CE/B1368) and a HRB postdoctoral fellowship (Grant No. PDTM/20011/9) awarded to MOCM. The Mass Spectroscopy Instrument and analysis was funded under the Higher Education Authority Programme for Research in Third-Level Institutions (PRTLI) and co-funded under the European Regional Development Fund.
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Additional Supporting Information may be found in the online version of this article:
Fig. S1. HPAEC-PAD analysis of post fermentation cell free supernatants of B. breve UCC2003, UCC2003-gal A and complemented strain. Modified Rogosa supplemented with 0.5 % GOS (A); post-fermentation supernatants of B. breve UCC2003 (B), UCC2003-galA-pBC1.2 (C) and UCC2003-galA-pBC1.2-galA (D).
Fig. S2. HPAEC-PAD analysis of post fermentation cell free supernatants of B. breve NCFB2257-pBC1.2, and GalA complemented derivative. Modified Rogosa supplemented with 0.5 % GOS (A); post-fermentation supernatants of B. breve NCFB2257-pBC1.2 (B) and B. breve NCFB2257-pBC1.2-galA (C).
Appendix S1. Experimental procedures.Click here for additional data file (mbt0006-0067-SD1.ppt)
Click here for additional data file (mbt0006-0067-SD2.doc)
Effect of PGOS on the transcriptome of B. breve UCC2003
|Locus tag_gene||Putative function||PGOSa|
|Bbr_0418_galD||Sugar permease protein||9.08|
|Bbr_0419_galE||Sugar permease protein||10.17|
|Bbr_0420_galG||β-Galactosidase GH 42 family||99.99|
|Bbr_0421_galR||Transcriptional regulator, LacI family||6.43|
|Bbr_1552_lacZ||β-Galactosidase GH 2 family||128.14|
|Bbr_1553_lacI||Transcriptional regulator, LacI family||2.9|
|Bbr_0526_gosR||Transcriptional regulator, LacI family||5.62|
|Bbr_0527_gosD||Sugar permease protein||8.75|
|Bbr_0528_gosE||Sugar permease protein||9.99|
|Bbr_0529_gosG||β-Galactosidase GH 42 family||6.33|
aExpression ratios presented have a Bayesian P-value < 0.001 according to the Cyber-T-test (Long et al., 2001).
Bacterial Strains and Plasmids used in this study
|Strain or plasmid||Relevant features||Reference or source|
|Escherichia coli strains|
|E. coli EC101||Cloning host, repA+ kmr||Law et al. (1995)|
|E. coli EC101-pNZ-M.BbrII + M.BbrIII||EC101 harbouring pNZ8048 derivative containing bbrIIM and bbrIIIM||O'Connell Motherway et al. (2009)|
|Bifidobacterium sp. strains|
|B. breve UCC2003||Isolate from nursling stool||Maze et al. (2007)|
|B. breve UCC2003-pBC1.2||UCC2003 harbouring pBC1.2||This study|
|B. breve UCC2003-galA||pORI19-tet-galA-967 insertion mutant of UCC2003||O'Connell Motherway et al. (2011b)|
|B. breve UCC2003-galA-pBC1.2-galA||pORI19-tet-galA-967 insertion mutant of UCC2003 harbouring complementationconstruct pBC1.2-galA||This study|
|B. breve UCC2003-galG||pORI19-tet-galG-410 insertion mutant of UCC2003||O'Connell Motherway et al. (2011b)|
|B. breve UCC2003-galC||pORI19-tet-galC-701 insertion mutant of UCC2003||O'Connell Motherway et al. (2011b)|
|B. breve UCC2003-gosD||pORI19-tet-bbr_0527 insertion mutant of UCC2003||This study|
|B. breve UCC2003-gosG||pORI19-tet-bbr_0529 insertion mutant of UCC2003||This study|
|B. breve UCC2003-lacS||pORI19-tet-bbr_1551 insertion mutant of UCC2003||This study|
|B. breve UCC2003-lacZ||pORI19-tet-bbr_1552 insertion mutant of UCC2003||This study|
|B. breve UCC2005||Isolate from human faeces||UCC|
|B. breve JCM7017||Isolate from human faeces||JCM|
|B. breve JCM7 019||Isolate from infant faeces||JCM|
|B. breve NCFB2257||Isolate from infant intestine||NCFB|
|B. breve NCFB2257-pBC1.2||NCFB2257 harbouring plasmid pBC1.2||This study|
|B. breve NCFB2257-pBC1.2-galA||NCFB2257 harbouring complementation construct pBC1.2-galA||This study|
|B. breve NCFB2258||Isolate from infant intestine||NCFB|
|B. breve LMG13208||Isolate from infant intestine||LMG|
|B. breve NCIMB11815||Isolate from infant intestine||NCTC|
|B. breve NCIMB8815||Isolate from human faeces||NCTC|
|B. breve NIZO658||Isolate from human faeces||NIZO|
|B. breve UCC2008||Isolate from infant intestine||UCC|
|B. breve UCC2009||Isolate from infant intestine||UCC|
|B. breve UCC2010||Isolate from human milk||UCC|
|Lactococcus lactis strains|
|L. lactis NZ9000||MG1363, pepN::nisRK, nisin-inducible overexpression host||de Ruyter et al. (1996)|
|L. lactis NZ9000-pNZ-Bbr_0010||NZ9000 containing pNZ-lacZ2||This study|
|L. lactis NZ9000-pNZ-gosG||NZ9000 containing pNZ-gosG||This study|
|L. lactis NZ9000-pNZ-galG||NZ9000 containing pNZ-galG||O'Connell Motherway et al. (2011b)|
|L. lactis NZ9000-pNZ-lacZ||NZ9000 containing pNZ-lacZ||This study|
|pAM5||pBC1-puC19-Tcr||Alvarez-Martín et al. (2007)|
|pBC1.2||pBC1-pSC101-Cmr||Alvarez-Martín et al. (2007)|
|pBC1.2-galA||pBC1-pSC101-Cmr harbouring galA including its own promoter||This study|
|pORI19||Emr, repA−, ori+, cloning vector||Law et al. (1995)|
|pORI19-tet-gosD||Internal 325 bp fragment of bbr_0527 and tetW cloned in pORI19||This study|
|pORI19-tet-gosG||Internal 395 bp fragment of bbr_0529 and tetW cloned in pORI19||This study|
|pORI19-tet-lacS||Internal 479 bp fragment of bbr_1551 and tetW cloned in pORI19||This study|
|pORI19-tet-lacZ||Internal 609 bp fragment of bbr_1552 and tetW cloned in pORI19||This study|
|pNZ8150||Cmr, nisin inducible translational fusion vector||Mierau and Kleerebezem (2005)|
|pNZ-lacZ2||Cmr, pNZ8150 derivative containing translational fusion of Bbr_0010 encoding DNA fragment to nisin inducible promoter||This study|
|pNZ-gosG||Cmr, pNZ8150 derivative containing translational fusion GosG encoding DNA fragment to nisin inducible promoter||This study|
|pNZ-galG||Cmr, pNZ8150 derivative containing translational fusion of GalG encoding DNA fragment to nisin inducible promoter||O'Connell Motherway et al. (2011b)|
|pNZ-lacZ||Cmr, pNZ8150 derivative containing translational fusion of LacZ encoding DNA fragment to nisin inducible promoter||This study|
JCM, Japan Collection of Microorganisms; LMG, Belgian Co-ordinated Collection of Microorganisms; NCFB, National Collection of Food Bacteria; NCTC, National Collection of Type Cultures; UCC, University College Cork Culture Collection.
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