Advances in the Production of Minor Ginsenosides Using Microorganisms and Their Enzymes
1Department of Biology, Faculty of Science and Technology, Universitas Airlangga, Surabaya, 60115, Indonesia
2Research Center for Bio-Molecule Engineering, Universitas Airlangga, Surabaya, 60115, Indonesia
*Correspondence: Almando Geraldi, Tel: +62-31-5936501; E-mail: firstname.lastname@example.org
Received: February 29 2020; Revised: March 19 2020; Accepted: April 27 2020; Published Online: May 29 2020
Cite this paper:
Almando Geraldi. Advances in the Production of Minor Ginsenosides Using Microorganisms and Their Enzymes. BIO Integration 2020; 1(1): 15–24.
This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/). See https://bio-integration.org/copyright-and-permissions/
Minor ginsenodes are of great interest due to their diverse pharmacological activities such as their anti-cancer, anti-diabetic, neuroprotective, immunomodulator, and anti-inflammatory effects. The miniscule amount of minor ginsenosides in ginseng plants has driven the development of their mass production methods. Among the various production methods for minor ginsenosides, the utilization of microorganisms and their enzymes are considered as highly specific, safe, and environmentally friendly. In this review, various minor ginsenosides production strategies, namely utilizing microorganisms and recombinant microbial enzymes, for biotransforming major ginsenosides into minor ginsenoside, as well as constructing synthetic minor ginsenosides production pathways in yeast cell factories, are described and discussed. Furthermore, the present challenges and future research direction for producing minor ginsenosides using those approaches are discussed.
biotransformation, biosynthesis, β-glucosidase, Ginsenosides, minor ginsenosides.
Ginseng, a plant belonging to the Araliaceae family and the genus Panax, has been used to treat different kinds of ailments and disease in East Asian countries for millennia [1, 2]. Recently, the popularity of ginseng as a nutraceutical and alternative medicine has been increasing worldwide [3, 4]. The global ginseng market has been reported to be valued at over two billion U.S. dollars and is expected to grow exponentially .
The beneficial health effects of ginseng are mainly attributed to ginsenosides, the major bioactive compound of ginseng [6, 7]. Various in vitro and in vivo studies have demonstrated the diverse pharmacological activities of ginsenosides such as anti-microbial, antioxidant, anti-inflammatory, skin-protective, neuroprotective, anti-cancer, and anti-diabetic effects (Table 1). Most of ginsenosides are classified as protopanaxadiol (PPD), and protopanaxatriol (PPT) types . Both types consist of an aglycon (a non-sugar component) of a dammarane skeleton (PPD or PPT) as an aglycon and one to four molecules of sugar moieties at C-3 and C-20 positions in the case of PPD-type ginsenosides or at C-6 and C-20 positions in the case of PPT-type ginsenosides [9, 10].
|Name||R1 (C3)||R3 (C20)||Health Benefits||References|
|Rb1||Major ginsenosides||Glc1–2Glc||Glc1–6Glc||Neuroprotective and anti-diabetic effects||[11, 12]|
|Rb2||Glc1–2Glc||Ara(p)1–6Glc||Neuroprotective and anti-inflammatory effects||[13, 14]|
|Rc||Glc1–2Glc||Ara(f)1–6Glc||Anti-inflammatory and skin-protective effects||[15, 16]|
|Rd||Glc1–2Glc||Glc–||Anti-cancer and neuroprotective effects||[17, 18]|
|F2||Minor ginsenosides||Glc–||Glc–||Anti-oxidant, anti-cancer, and skin-protective effects||[19–21]|
|Rg3||Glc1–2Glc||H||Anti-depressant, anti-virus, and anti-cancer effects||[22–24]|
|Gypenoside XVII (GypXVII)||Glc–||Glc1–6Glc||Cardioprotective and neuroprotective effects||[25, 26]|
|Gypenoside LXXV (GypLXXV)||H–||Glc1–6Glc||Skin-protective and anti-cancer effects||[27, 28]|
|Rh2||Glc–||H–||Skin protective, immunomodulator, anti-virus, and anti-cancer effects||[29–32]|
|Compound K (CK)||H||Glc–||Anti-epileptic, anti-cancer, and skin-protective effects||[33–35]|
|Name||R2 (C6)||R3 (C20)||Health Benefit||References|
|Re||Major ginsenosides||Rha1–2Glc||Glc–||Anti-diabetic, kidney-, and heart-protective effects||[36–38]|
|Rf||Glc1–2Glc||H||Neuroprotective and anti-inflammatory effects||[39, 40]|
|Rg1||Glc–||Glc–||Neuroprotective and hepatoprotective effects||[41, 42]|
|Rg2||Minor ginsenosides||Rha1–2Glc||H-||Skin-protective, antidepressant, and anti-inflammatory effects||[43–45]|
|Rh1||Glc-||H||Anti-oxidant, anti-inflammatory, immunomodulator, and anti-cancer||[46, 47]|
|F1||H||Glc-||Anti-aging, anti-oxidant, skin-protective, immunomodulator||[48, 49]|
Ara(f): α-l-arabinofuranosyl; Ara(p): α-l-arabinopyranosyl; Glc: α-d-glucopyranosyl; Rha: α-l-ahamnopyranosyl.
Meanwhile, based on their abundance in ginseng, ginsenosides can be classified as major ginsenoside and minor ginsenosides. Major ginsenosides [i.e., Rd, Rc, Rb2, and Rb1 (PPD-type); Rg1, Rf, and Re (PPT-type)] constitute more than 90% of the total ginsenosides, while minor ginsenosides [i.e. F2, Rg3, Rh2, and Compound K (PPD-type); Rg2, Rh1, and F1 (PPT-type)] are only present in small quantities in ginseng [50, 51]. Despite showing some therapeutic effects such as, anti-inflammatory, anti-diabetic, and neuroprotective effects, major ginsenosides are not easily absorbed by the human body . On the other hand, while they are only present in very low amounts in ginseng, minor ginsenosides are considered as being more pharmacologically active than major ginsenosides due to their smaller molecule size, better permeability across the cell membrane, and thus their higher bioavailability [53, 54].
Minor ginsenosides are of commercial interest due to their diverse biological activities and high pharmacological activities. However, the miniscule amount of minor ginsenosides extracted from ginseng cannot satisfy the needs of scientific and clinical studies, as well as commercial purposes [55, 56]. Therefore, it is very important to develop useful methods for the mass production of minor ginsenosides.
Minor ginsenosides production methods
The most common approach to producing minor ginsenosides is by hydrolyzing the sugar moieties of major ginsenosides . The hydrolysis can be conducted through physical (heat and microwave transformation), chemical (acid and alkali hydrolysis), and biological (biotransformation) methods. Heat transformation via baking and steaming transforms PPD-type major ginsenosides Rb1, Rb2, and Rc2 into Rd, and finally into minor ginsenosides Rg3, F2, compound K, and Rh2, as well as PPT-type major ginsenosides Re and Rf into minor ginsenosides Rh1 and F1, with by-products of acetyl-ginsenosides [58, 59]. Meanwhile, acid hydrolysis using hydrochloric acid transformed Rb1 into Rg3 . The physical and chemical methods are considered to be fast and simple; however, the use of those methods often results in the formation of undesirable by-products due to the low specificity. Moreover, there are safety and environmental issues, for example, due to the use of high temperature in the heat transformation approach, or strong acid/base in the acid/alkali hydrolysis methods. On the other hand, biological methods which involve enzymes offer higher reaction specificity, can be conducted in mild conditions minimizing safety risks, and are more environmentally friendly . Thus, there is growing interest in using biological methods for the mass production of minor ginsenosides.
In general, the biological methods for producing minor ginsenosides can be categorized as; the use of microbial cells and enzymes for hydrolyzing sugar moieties of major ginsenosides, and the emerging biosynthesis methods, where the minor ginsenoside biosynthesis pathway is introduced into microorganism hosts. The present paper reviews the advances on using those biological methods for producing minor ginsenosides.
Biotransformation of major ginsenosides into minor ginsenosides using microorganisms
A wide variety of microorganisms have been used in the biotransformation of major ginsenosides into minor ginsenosides (Table 2). The biotransformation activities are mainly attributed to β-glucosidases (β-d-glucopyranoside glucohydrolase) [E.C.220.127.116.11] which hydrolyze the glycosidic bonds of the sugar moieties of the major ginsenosides at the C-3, C-6, and C-20 positions . However, due to specific structures of the aglycon (dammarane skeleton), only specific β-glucosidases, thus specific microorganisms are able to hydrolyze ginsenoside-β-glucoside linkages .
|Microorganism||Source of Microorganism||Transformation Pathway||Remarks|
|Flavobacterium sp. GE 32 ||Root of Panax ginseng (Jilin, China)||Rb1 → GypXVII
Rb1 → Rd → Rg3
|Burkholderia sp. GE 17–7 ||P. ginseng (Jilin, China)||Rb1 → Rd → Rg3||Rg3 was produced with conversion rate of 98% after 15 h|
|Arthrinium sp. GE 17–18 ||Root of P. ginseng (Jilin, China)||Rb1 → Rd → F2 → CK||Endophytic fungi|
|Cellulosimicrobium sp. TH-20 ||Soil of ginseng field (Fusong, China)||Re → Rg2||Re (30 mg) was transformed into Rg2 (24 mg) with a yield of 96%|
|C. allociferrii JNO301 ||Meju (dried fermented soybeans) from South Korea||Rb1 → Rd → F2
Rf → Rh1
|Leuconostoc mesenteroides WIKim19 ||Kimchi (fermented vegetable) from South Korea||Rb1 → Rd → Rg3||–|
|Lactobacillus rhamnosus GG ||Culture collection||Rb1 → Rd||Probiotic microorganism|
|Schizophyllum commune ||Culture collection||Rb1 → Rd → F2 → CK||Edible and medicinal fungi|
Ginseng plantation fields are one of the main sources of microorganisms with major ginsenoside-biotransforming activities. Endophytic microorganisms, spend all or part of their life cycle inside ginseng plants without damaging the plant tissues or inducing defense responses, for example, Burkholderia sp. GE 17-7 and Flavobacterium sp. GE 32, as well as fungi Arthrinium sp. GE 17-18 . Those microorganisms exhibit hydrolysis activities on PPD-type ginsenosides. Flavobacterium sp. GE 32 has been reported to hydrolyze the outer glycosidic linkage of Rb1 at C-3 to produce Gypenoside XVII and the C-20 position to produce Rd. The bacteria also showed hydrolysis activities on the glycosidic linkage at the C-20 position of Rd to generate Rg3 . Similar hydrolysis activities on the terminal and inner glucopyranosyl moieties at the C-20 position of Rb1 to produce Rg3 were also shown by Burkholderia sp. GE 17-7 . Meanwhile Arthrinium sp. GE 17-18 was shown to have hydrolysis activity on terminal and inner glucopyranosyl moieties at the C-3 position and terminal glucopyranosyl moieties at the C-20 position of Rb1 to generate CK . Finally, Cellulosimicrobium sp. TH-20 isolated from rhizosphere soil of ginseng showed biotransformation activities on PPT-type Re to Rg2 by hydrolyzing sugar moieties at the C-20 position .
Generally recognized as safe (GRAS) microorganisms (i.e., probiotics, microorganisms from fermented foods, etc.), which are non-pathogenic and considered as safe to be used for nutraceutical and pharmaceutical purposes, were also reported to have major ginsenoside-biotransforming activities . Candida allociferrii JNO301 yeast isolated from Korean fermented soybean showed hydrolysis activity on outer glucopyranosyl moieties at the C-3 and C-20 positions of Rb1 to produce F2. Interestingly the yeast also exhibited biotransformation activity on PPT-type ginsenoside Rf into Rh1, by hydrolyzing outer sugar moieties at the C-6 position .
Biotransformation of major ginsenosides into minor ginsenosides using β-glucosidase from microorganisms
Purified recombinant enzymes are considered superior to the enzymes isolated and purified from cultured microorganisms due to their higher selectivity and activity [74–76]. Gram-scale quantities of minor ginsenosides were produced using enzymes from Microbacterium sp. Gsoil 167 isolated from ginseng plantation and Lactobacillus ginsenosidimutans EMML 3041 from kimchi (fermented vegetable) [27, 77] (Table 3). Thermostable β-glucosidase were also reported to exhibit ginsenoside-biotransformation activities which resulted in the production of Gram-scale quantities of minor ginsenosides. Those thermostable enzymes are of industrial interest as the enzymes can be used in combination with heat and acid hydrolysis to further accelerate and increase the yield of major ginsenoside biotransformation. While most of ginsenoside-biotransforming microorganisms and enzymes are isolated from the East Asia region, interestingly one bacterial isolate from Indonesia has β-glucosidase that can hydrolyze the outer sugar moieties at C-3 and C-20 of Rb1 to produce F2 .
|β-Glucosidase||Source of Microorganism||Transformation Pathway||Yields|
|Recombinant β-glucosidase from Microbacterium sp. Gsoil 167 expressed in E. coli BL21(DE3) ||Soil of ginseng field (Pocheon, South Korea)||•||GypXVII → GypLXXV||•||GypXVII (10 g) was transformed into GypLXXV (5.7 g; 69.6% recovery; and 97.8 chromatography purity)|
|Recombinant β-glucosidase from Arachidicoccus ginsenosidimutans sp. nov. expressed in E. coli BL21(DE3) ||Ginseng compost (South Korea)||•||Rb1 → GypXVII → F2 → CK||–|
|•||Rd → F2|
|Recombinant β-glucosidase from Microbacterium esteraromaticum expressed in E. coli BL21(DE3) ||Soil of ginseng field (South Korea)||•||Re → Rg2||•||Re (1 mg) was transformed into Rg2 (0.83 mg; 100% molar conversion yield within 150 min)|
|•||Rg1 → Rh1|
|•||Rg1 (1 mg) was transformed into Rh1 (0.6 mg; 78% molar conversion yield within 15 min)|
|Recombinant β-glucosidase from M. esteraromaticum expressed in E. coli BL21(DE3) ||Soil of ginseng field (South Korea)||•||Rb1 → Rd → CK||•||Rb1 (1 mg/ml) was transformed into CK (0.46 mg/ml; 77% molar conversion yield within 60 min)|
|Recombinant β-glucosidase from Pseudonocardia sp. Gsoil 1536 expressed in E. coli BL21(DE3) ||Soil of ginseng field (Pocheon, South Korea)||•||Re → Rg2||•||Re (150 g) was transformed into Rg2 (150 g; 84.0±1.1% chromatographic purity)|
|Recombinant β-glucosidase from Lactobacillus brevis expressed in E. coli BL21(DE3) ||Kimchi (fermented vegetable) from South Korea||•||GypXVII → CK||•||GypXVII was transformed into CK (89% molar conversion yield within 6 h)|
|Recombinant β-glucosidase from L. ginsenosidimutans EMML 3041 expressed in E. coli BL21(DE3) ||Kimchi (fermented vegetable) from South Korea||•||Rb1 → Rd → Rg3||•||Rb1 (50 g) was transformed into Rg3 (30 g; 74.3% chromatographic purity)|
|Recombinant β-glucosidase from Thermotoga thermarum DSM 5069 expressed in E. coli JM109 (DE3) ||Culture Collection||•||Re → Rg2||•||Re (10 g/L) was transformed into Rg2 (8.02 g/L) within 60 min at 85 °C and PH 5.5.|
|•||Rg1 → Rh1|
|•||Rg1 (2 g/L) was transformed into Rh1 (1.56 g/L) within 60 min at 85 °C and PH 5.5|
|Recombinant β-glucosidase from Caldicellulosiruptor bescii in E. coli ||Culture Collection||•||Rb1 → Rd → F2 → CK||•||CK was produced from Rb1 with the productivity of 1000 (μM/h) within 80 min at 80 °C and PH 5.5|
|•||Rc → Rd → F2 → CK|
|•||CK was produced from Rc with the productivity of 400 (μM/h) within 180 min at 80 °C and and PH 5.5|
|Recombinant β-glucosidase from Thermotoga neapolitana DSM 4359 in E. coli ||Culture Collection||•||Re → Rg2||•||Re (2 mg/ml) was transformed into Rg2 (1.66 mg/ml; 100% molar conversion yield) within 3 h at 85 °C and PH 5.5|
|Recombinant β-glucosidase from Serratia marcescens LII61 expressed in E. coli BL21(DE3) ||Slaughterhouse waste (Indonesia)||•||Rb1 → Rd → F2||–|
|•||Rb1 → GypXVII → F2|
|Recombinant β-glucosidase from M. testaceum ATCC 15829 expressed in C. glutamicum ATCC 13032 ||Culture Collection||•||Rb1 → GypXVII → GypLXXV → F2 → CK||•||CK (7.59 g/L) was produced from PPD-type ginsenoside mixtures in 24 h|
|•||Rd → F2 → CK|
|•||Re → F1||•||F1 (9.42 g/L) was produced from PPT-type ginsenoside mixtures in 24 h|
|•||Rg → F1|
|Recombinant β-glucosidase from Paenibacillus mucilaginosus KCTC 3870 expressed in C. glutamicum ATCC 13032 ||Culture Collection||•||Rg3 → Rh2||–|
|Recombinant β-glucosidase from Flavobacterium johnsoniae expressed in L. lactis subsp. cremoris NZ9000 ||Culture Collection||•||Rb1 → Rd → F2 → CK||–|
|•||Rb1 → Rd → Rg3|
|Recombinant β-glucosidase from P. mucilaginosus expressed in L. lactis subsp. cremoris NZ9000 ||Culture Collection||•||Rb1 → Rd → F2||•||F2 was produced from PPD-type ginsenoside mixtures with 74% conversion yield|
Based on the data in Table 3, Escherichia coli is the most common host for the production of recombinant β-glucosidase. This is due to the simplicity of E. coli genetic modification and its rapid growth in relatively inexpensive media [78, 79]. However, E. coli is not preferable for application in food and pharmaceutical industries due to its non-GRAS status . Efforts to produce ginsenoside transforming-β-glucosidase in GRAS microorganisms, such as Corynebacterium glutamicum and Lactococcus lactis have been attempted. Microbacterium testaceum β-glucosidase was successfully expressed in C. glutamicum and exhibit biotransformation activity for both PPD- and PPT-type ginsenosides, and resulted in the production of Gram-scale quantities of CK and F1 . However, in general, the quantity and activity of ginsenoside biotransforming-β-glucosidases produced in GRAS hosts are not as high as recombinant β-glucosidases produced in E. coli [81, 82].
Biosynthesis of minor ginsenoside in microorganisms
Despite the high efficiency, biotransformation methods for producing minor ginsenosides require ginseng extracts as the raw material which are produced through time-consuming (typically, 5–6 years are required to produce marketable ginseng), labor-intensive, energy-consuming, and high-cost processes and can be affected by many factors such as soil quality, climate, pathogens, and pests [92, 93]. The discovery of genes encoding enzymes involved in the minor ginsenosides synthesis pathway coupled with the advances in synthetic biology tools, has allowed the construction of microbial cell factories, which can provide more sustainable and cost-effective alternative to mass-produced minor ginsenosides from renewable resources [94, 95].
The ginsenoside biosynthesis pathway has mainly been introduced for three species of yeasts (Saccharomyces cerevisiae, Pichia pastoris, and Yarrowia lipolytica) which are on the GRAS list of microorganisms, and are compatible for the expression of plant-derived heterologous enzymes . In general, there are three general strategies to produce minor ginsenosides in yeast cell factories: (1) improving the yield of the yeast native mevalonic acid (MVA) pathway; (2) introducing genes for the synthesis of ginsenosides aglycons; and (3) introducing uridine diphosphate (UDP)-glycosyltransferase genes for the addition of sugar moieties to the aglycons (Figure 1).
The MVA pathway produces isopentenyl pyrophosphate (IPP) and dimethylallyl pyrophosphate (DMAPP) which are important precursors for the synthesis of ginsenosides, from acetyl coenzyme A (acetyl-CoA). The native MVA pathway of yeasts is improved by overexpressing 3-hydroxy-3-methylglutaryl-CoA reductase (HMGR) which catalyzes the production of mevalonate from 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA). Furthermore, to eliminate the post-transcriptional feedback inhibition, hmgr gene with a truncated N-terminal (thmgr), which lacks its N-terminal transmembrane sequence coding for membrane-binding activity, is used . Additionally, the acetyl-CoA supply to the pathway can be improved, for example, via the overexpression of the ALD6 gene (encoding NADP-dependent aldehyde dehydrogenase) along with the introduction of a synthetic codon-optimized acetyl-CoA synthase mutant from Salmonella enterica .
IPP and DMAPP are then converted to 2,3 oxidosqualene, the precursor of ginsenoside aglycons. The yield of 2,3 oxidosqualene is improved by the overexpression of squalene synthase (SQS)- and squalene epoxidase (SQE)-encoding genes. To minimize the utilization of 2,3 oxidosqualene by competing yeasts in the native ergosterol pathway, downregulation of the Erg7/LS (lanosterol synthase)-encoding gene is conducted. The subsequent conversion of 2,3 oxidosqualene into dammarenediol and protopanaxadiol/protopanaxatriol was facilitated by the introduction of dammarenediol II synthase and cytochrome P450 (CYP) [protopanaxadiol synthase (CYP716A47) and protopanaxatriol synthase (CYP716A53v2)] genes from P. ginseng and NADPH-cytochrome P450 reductase (CPR) from Arabidopsis thaliana or P. ginseng [92, 98, 99].
Finally, the addition of sugar moieties to PPD and PPT aglycons was facilitated by the introduction of glycosyltransferases-encoding genes. UDP-glycosyltransferases from P. ginseng, PgUGT45 and PgUGT74AE2, catalyze the transfer of a glucose moiety from UDP-glucose (UDP-Glc) to the C3 hydroxyl groups of PPD to form Rh2, whereas PgUGT29 and PgUGT94Q2 catalyze the transfer of a glucose moiety from UDP-Glc to Rh2 to form Rg3 [100, 101]. Meanwhile, PgUGT100 and PgUGT1 transfer a glucose moiety from UDP-glucose (UDP-Glc) to the C-6 and C-20 hydroxyl groups of PPT to form Rh1 and F1, respectively . The application of the general strategies along with other strategy such as protein engineering resulted in the production of minor ginsenoside in Gram-scale quantities (Table 4).
|S. cerevisiae strain BY4742 (MATα, his3Δ1, leu2Δ0, lys2Δ0, ura3Δ0)||•||Enhancing MVA pathway of S. cerevisiae strain BY4742||Rh2, Rg3||Rg3 (3.49 ± 0.14 μmol/g dry cell weight) and Rh2 (1.45 ± 0.27 μmol/g dry cell weight) were produced after 6 days |
|•||Introducing dammarenediol synthase gene and protopanaxadiol synthase genes and UDP-glycosyltransferase genes from P. ginseng (PgUGT45 and PgUGT29) into S. cerevisiae strain BY4742|
|S. cerevisiae strain ZW-PPD-B (PPD-producing yeast strain) ||•||Introducing cytochrome P450 CYP716A53v2, cytochrome P450 reductase PgCPR1, and UDP-glycosyltransferase PgUGT100 genes into S. cerevisiae strain ZW-PPD-B to construct an Rh1-producing yeast strain||Rh1, F1||Rh1 (92.8 ± 12.5 mg/L) and F1 (42.1 ± 3.2 mg/L) were produced after 6 days |
|•||Introducing CYP716A53v2, PgCPR1, and PgUGT1 genes into S. cerevisiae strain ZW-PPD-B to construct an F1-producing yeast strain|
|S. cerevisiae strain ZD-PPD-016 (PPD-producing yeast strain) ||•||Conducting site-directed mutagenesis and iterative saturation mutagenesis to S. cerevisiae glycosyltransferase-encoding gene (UGT51)||Rh2||Rh2 (300 mg/L) was produced via a 5 L fed-batch fermentation |
|•||Introducing mutant UGT51 gene into S. cerevisiae strain ZD-PPD-016 to construct an Rh2-producing yeast strain|
|S. cerevisiae strain BY4742 (MATα, his3Δ1, leu2Δ0, lys2Δ0, ura3Δ0)||•||Modular engineering of the MVA pathway||Rh2||Rh2 (2.25 g/L) was produced via a 10 L fed-batch fermentation |
|•||Optimizing the expression level of cytochrome P450|
|•||Increasing the copy number of UDP-glycosyltransferase-encoding gene (UGTPg45 from P. ginseng) and engineering its promoter to increase the expression level of the enzyme|
|•||Conducting in vivo directed evolution to the in vivo activity of UGTPg45 in yeast|
|Y. lipolytica ATCC 201249||•||Overexpressing key genes in the MVA pathway||CK||CK (161.8 mg/L) was produced via 5 L fed-batch fermentation |
|•||Constructing fusion of cytochrome NADPH-P450 reductase, and P450 monooxygenase (PPDS), and introducing the gene into Y. lipolytica ATCC 201249|
|•||Introducing UDP-glycosyltransferase genes UGT1 from P. ginseng into Y. lipolytica ATCC 201249|
MVA: Mevalonic acid.
Conclusion and future perspectives
Due to their medical importance and high economical value, investigations on the mass-production methods of minor ginsenosides, especially those that involve microorganisms and their enzymes, have garnered great interest. Various microorganisms have been reported to be able to convert major ginsenosides into minor ginsenosides, including GRAS microorganisms which would be suitable for the food and drugs industries. To date the highest yield of minor ginsenosides has been obtained via the biotransformation of major ginsenosides using recombinant β-glucosidase expressed in E. coli systems. However, E. coli is considered as unsafe, and is an inedible bacteria, which would limit its application in the nutraceutical and pharmaceutical industries. Thus, the improvements of recombinant β-glucosidase production in GRAS strains such as C. glutamicum and L. lactis, for example, through the optimization of growth condition, and media, as well as genetic engineering, are needed.
Finally, the costly, time-consuming, and labor-intensive process of producing ginseng extract as substrates for biotransformation, has driven the development of more sustainable ways to produce minor ginsenosides, especially via biosynthesis in yeast cell factories. The introduction of ginsenosides biosynthesis genes from P. ginseng coupled with the optimization of yeast native pathways has led to the successful production of minor ginsenosides. Further optimization using protein engineering, synthetic biology, and metabolic engineering approaches, as well as the development of efficient fermentation strategies are critical to unleash the full potential of yeast cell factories to mass produce minor ginsenosides.
The authors declare that they have no competing interests.
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