5. Bioconversion of Ginsenosides by β-Glucosidase Enzymes Obtained from Microorganism
Bacteria, fungi, and yeast have been identified in the bioconversion of ginsenosides (
Table 1)
[8][49][50][60][61][62][8,20,66,67,76,77]. The isolation and purification of β-glucosidase are time-consuming and expensive processes. Therefore, whole-cell protein preparations are frequently used in the bioconversion of ginsenosides, despite the low enzymatic activity within the preparation and the presence of numerous other undefined factors. The β-glucosidase activity of a microorganism can be examined via ginsenoside conversion and minor ginsenoside synthesis. In this case, the bacteria were cultivated under artificial conditions using ginsenosides as a carbon source.
The activity of β-glucosidase can be manipulated during fermentation process by adjusting ginsenoside types, reaction concentration of enzyme or substrate, ion, pH, or temperature. Multiple studies have demonstrated that the optimal reaction conditions depend on the bacterial strains used and the rate of microbial growth that influence the reaction’s activity
[5][9][10][43][5,9,10,14]. After induction of microbial biotransformation, the functionalities of fermented ginsenosides are assessed. Antioxidant activity is common among compounds extracted from medicinal plants. Compared to non-fermented ginseng, fermented ginseng shows greater hydroxyl radical scavenging and antioxidant activity. Minor ginsenosides derived from Rb1 or Rc, such as Rd, inhibit lipid oxidation and suppress the antioxidant defense system in various in vitro assays
[2].
Anti-cancer activity, in particular, is of great interest for human applications. Anticancer effects of
P. ginseng minor (but not major) ginsenoside have been demonstrated in vitro, in vivo, ex vitro, and ex vivo in both animal and human cancer cell lines
[2][23][27][33][51][2,29,40,46,68].
In addition to using ginsenosides as the primary source material, β-glucosidase can also be used to synthesize a few minor ginsenoside structures, although the mechanism is unknown.
6. Bioconversion of Ginsenoside by Recombinant β-Glucosidases
While whole-cell preparations for ginsenosides biotransformation are fairly simple to prepare and use, it is difficult to regulate off-target processes and perform glycosides hydrolysis for selective enrichment of ginsenosides. It is also difficult for the food and cosmetics industries achieve a large-scale safe approach due to challenges such as scarcity of microorganisms certified to be generally recognized as safe (GRAS), the difficulty of scaling up fermentation, the slow reaction rate, and the presence of novel end products
[2][9][10][2,9,10]. These restrictions can be overcome by using purified recombinant β-glucosidase, which has been shown to be extremely effective and has a short reaction time to high yields. Studies using β-glucosidase recombinant enzymes have shown successful conversion of ginsenosides almost reported in GH1 and GH3 family. Differences in amino acid sequence, structure, and interactions are among the many factors that contribute to the specificity of enzymes with substrates
[5][10][15][53][5,10,24,28].
Nonetheless, the lack of acceptable hots for recombinant expression of β-glucosidase has hampered the adoption of food-grade preparations. The majority of studies of recombinant β-glucosidase gene expression and bioconversion of ginsenosides continues to employ the
E. coli system as a host, which is a significant barrier to the continued implementation of recombinant enzymes in high-quality food products.
Several landmark studies of β-glucosidase expression in GRAS organism have hinted at its potential for enhancing the nutritional content and quality of food, pharmaceuticals, and functional foods
[33][44][48][63][64][46,57,61,65,80]. However, there are limitations that must be overcome for the large-scale use of β-glucosidase in these ways. There are extreme circumstances, such as pH, temperature, and concentrations of enzyme and substrate, and the difficulty of isolation and purification recombinant enzyme applications
[19][22][25][29][31][35][46][51][65][66][67][68][33,36,38,42,44,48,63,68,72,73,88,89].
7. Other Methods for Ginsenoside Bioconversion
Ginsenosides may be converted not only by biological methods but also by physical and chemical approaches. Many mechanisms are involved in the physical transformation of saponin composition, notably of the sugar moiety. In addition, several physical methods can successfully transform ginsenosides, namely heating, steaming, air-drying, sulfur fumigation, high hydrostatic pressure (HHP), and microwave treatment. However, with the exception of steaming, these processes have not yet been applied commercially
[12][23][51][69][70][12,29,68,84,94]. Regarding chemical methods, acidic and alkaline hydrolysis at high temperatures, high pressure, and high pH has been used to the cleave or degrade major ginsenosides into minor ginsenosides for increased biological and pharmacological activity. Nonetheless, it is challenging to control the side reactions and implement the hydrolysis of glycosylation for selective ginsenoside enrichment
[8][12][71][8,12,95].