Abstract

The supernatants (the solution part received after centrifugation) of squid pens fermented by four species of Paenibacillus showed potent inhibitory activity against α-glucosidases derived from yeast (79–98%) and rats (76–83%). The inhibition of acarbose—a commercial antidiabetic drug, used against yeast and rat α-glucosidases—was tested for comparison; it showed inhibitory activity of 64% and 88%, respectively. Other chitinolytic or proteolytic enzyme-producing bacterial strains were also used to ferment squid pens, but no inhibition activity was detected from the supernatants. Paenibacillus sp. TKU042, the most active α-glucosidase inhibitor (aGI)-producing strain, was selected to determine the optimal cultivation parameters. This bacterium achieved the highest aGI productivity (527 µg/mL) when 1% squid pens were used as the sole carbon/nitrogen source with a medium volume of 130 mL (initial pH 6.85) in a 250 mL flask (48% of air head space), at 30 °C for 3–4 d. The aGI productivity increased 3.1-fold after optimization of the culture conditions. Some valuable characteristics of Paenibacillus aGIs were also studied, including pH and thermal stability and specific inhibitory activity. These microbial aGIs showed efficient inhibition against α-glucosidases from rat, yeast, and bacteria, but weak inhibition against rice α-glucosidase with IC50 values of 362, 252, 189, and 773 µg/mL, respectively. In particular, these aGIs showed highly stable activity over a large pH (2–13) and temperature range (40–100 °C). Various techniques, including: Diaoin, Octadecylsilane opened columns, and preparative HPLC coupled with testing bioactivity resulted in isolating a main active compound; this major inhibitor was identified as homogentisic acid (HGA). Notably, HGA was confirmed as a new inhibitor, a non-sugar-based aGI, and as possessing stronger activity than acarbose with IC50, and maximum inhibition values of 220 μg/mL, 95%, and 1510 μg/mL, 65%, respectively. These results suggest that squid pens, an abundant and low-cost fishery processing by-product, constitute a viable source for the production of antidiabetic materials via fermentation by strains of Paenibacillus. This fermented product shows promising applications in diabetes or diabetes related to obesity treatment due to their stability, potent bioactivity, and efficient inhibition against mammalian enzymes.

Highlights

  • Squid pens (SP), a chitinous marine material obtained as by-products from seafood processing, have been used to produce various bioactive materials via microbial conversion

  • To investigate the potency of active α-glucosidase inhibitor (aGI) production by the genus Paenibacillus, four novel species of Paenibacillus were cultivated in a medium containing 1% squid pens powder (SPP) before the culture supernatants of fermented SPP (FSPP) were tested for activity

  • The function of Paenibacillus species as aGI producers was investigated based on recent literature reviews

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Summary

Introduction

Squid pens (SP), a chitinous marine material obtained as by-products from seafood processing, have been used to produce various bioactive materials via microbial conversion. Diabetes mellitus (DM) is recognized as a continuing and growing health issue, seriously reducing the quality of people’s health worldwide [9] This disease has become a major cause of death, responsible for 8.4% of total deaths in 2013 [10]. It has been reported that aGIs are difficult to obtain in large amounts from herbs [14], while synthesized aGIs, able to be produced on a large scale, often cause side effects [15]. Microbial conversion may offer another means of obtaining natural aGIs with promising activity, providing an alternative to commercially available inhibitors—such as acarbose, miglitol, and voglibose—which have been reported to cause side effects [16]. The specific inhibitory activity, stability of the aGIs, and the major active compound were investigated

Results and Discussion
Effects of Cultivation Time and Supplementary Air on aGI Productivity
Theof of aGI is similar that of bacterial
Effects of Some Parameters on aGI Productivity
Specific Inhibition of FSPP
Materials
Enzymatic Inhibitory Assay
Effects of Additional Parameters on aGI Productivity
Measurement of pH and Thermal Stability
Conclusions
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