Study on differences in carbohydrate utilization between tropical and nontropical derived Lactiplantibacillus plantarum

  • CHEN Shiqian ,
  • ZHANG Chengcheng ,
  • YU Leilei ,
  • WANG Ruimin ,
  • ZHAI Qixiao
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  • 1(School of Food Science and Technology, Jiangnan University, Wuxi 214122, China)
    2(School of Food Science and Engineering, Hainan University, Haikou 570228, China)

Received date: 2025-05-12

  Revised date: 2025-07-04

  Online published: 2026-03-25

Abstract

Lactiplantibacillus plantarum exhibits extensive carbohydrate metabolic capabilities.This study compared the distribution of carbohydrate-active enzyme (CAZy) genes, differential carbohydrate utilization, and variations in free amino acid content during green pepper fermentation between tropical and nontropical strains.Key findings revealed that tropical strains possessed a significantly higher average number of glycosyltransferase (GT) family genes (310±13) compared to nontropical strains (296±5, P<0.05), with GT2 and GT4 families being particularly enriched.Tropical strains showed superior rhamnose metabolism[shorter generation time:(0.62±0.11) h vs.(1.35±0.27) h, P<0.05] but weaker utilization of sucrose[generation time:(1.43±0.06) h vs.(1.09±0.06) h) and fructose[(1.42±0.09) h vs.(1.03±0.09) h, P<0.01].No significant differences were observed for xylose, maltose, stachyose, or glucose (P>0.05).Fermented green peppers inoculated with tropical strains contained higher levels of arginine[(5.15±0.11) mg/100 g vs.(2.69±0.75) mg/100 g] and serine[(2.09±0.22) mg/100 g vs.(0.83±0.53) mg/100 g] compared to nontropical strains (P≤0.05).Notably, arginine content exceeded that of the commercial control[(2.10±0.36) mg/100 g, P≤0.001].Geographic origin drives adaptive divergence in CAZy genes (particularly GT families) of L.plantarum, providing a rationale for developing region-specific probiotics.

Cite this article

CHEN Shiqian , ZHANG Chengcheng , YU Leilei , WANG Ruimin , ZHAI Qixiao . Study on differences in carbohydrate utilization between tropical and nontropical derived Lactiplantibacillus plantarum[J]. Food and Fermentation Industries, 2026 , 52(5) : 132 -138 . DOI: 10.13995/j.cnki.11-1802/ts.043258

References

[1] 王佳, 郑诗琪, 冯鑫, 等.植物乳植杆菌AR113利用碳源情况研究[J].食品与发酵工业, 2023, 49(11):1-6.
WANG J, ZHENG S Q, FENG X, et al.Research of carbon source utilization by Lactiplantibacillus plantarum AR113[J].Food and Fermentation Industries, 2023, 49(11):1-6.
[2] KLEEREBEZEM M, BOEKHORST J, VAN KRANENBURG R, et al.Complete genome sequence of Lactobacillus plantarum WCFS1[J].Proceedings of the National Academy of Sciences of the United States of America, 2003, 100(4):1990-1995.
[3] BUNTIN N, HONGPATTARAKERE T, RITARI J, et al.An inducible operon is involved in inulin utilization in Lactobacillus plantarum strains, as revealed by comparative proteogenomics and metabolic profiling[J].Applied and Environmental Microbiology, 2016, 83(2):e02402-16.
[4] FUHREN J, RÖSCH C, TEN NAPEL M, et al.Synbiotic matchmaking in Lactobacillus plantarum:Substrate screening and gene-trait matching to characterize strain-specific carbohydrate utilization[J].Applied and Environmental Microbiology, 2020, 86(18):e01081-20.
[5] SIEZEN R J, TZENEVA V A, CASTIONI A, et al.Phenotypic and genomic diversity of Lactobacillus plantarum strains isolated from various environmental niches[J].Environmental Microbiology, 2010, 12(3):758-773.
[6] MAO B Y, YIN R M, LI X S, et al.Comparative genomic analysis of Lactiplantibacillus plantarum isolated from different niches[J].Genes, 2021, 12(2):241.
[7] CUI Y H, WANG M H, ZHENG Y K, et al.The carbohydrate metabolism of Lactiplantibacillus plantarum[J].International Journal of Molecular Sciences, 2021, 22(24):13452.
[8] LOMBARD V, GOLACONDA RAMULU H, DRULA E, et al.The carbohydrate-active enzymes database (CAZy) in 2013[J].Nucleic Acids Research, 2014, 42(Database issue):D490-D495.
[9] WARDMAN J F, BAINS R K, RAHFELD P, et al.Carbohydrate-active enzymes (CAZymes) in the gut microbiome[J].Nature Reviews Microbiology, 2022, 20(9):542-556.
[10] ABOT A, ARNAL G, AUER L, et al.CAZyChip:Dynamic assessment of exploration of glycoside hydrolases in microbial ecosystems[J].BMC Genomics, 2016, 17(1):671.
[11] PENGTHAISONG S, PINIELLO B, DAVIES G J, et al.Reaction mechanism of glycoside hydrolase family 116 utilizes perpendicular protonation[J].ACS Catalysis, 2023, 13(9):5850-5863.
[12] HUANG L, WANG Y, ZHONG K Y, et al.In vitro characterization and identification of potential probiotic yeasts isolated from zaopocu, a traditional fermented dregs vinegar from Hainan Island[J].Probiotics and Antimicrobial Proteins, 2024.DOI:10.1007/s12602-024-10347-8.
[13] LI K N, WANG S J, LIU W J, et al.Comparative genomic analysis of 455 Lactiplantibacillus plantarum isolates:Habitat-specific genomes shaped by frequent recombination[J].Food Microbiology, 2022, 104:103989.
[14] SMITS S A, LEACH J, SONNENBURG E D, et al.Seasonal cycling in the gut microbiome of the Hadza hunter-gatherers of Tanzania[J].Science, 2017, 357(6353):802-806.
[15] RAPOPORT A E, TRIFONOV E N.“Anticipated” nucleosome positioning pattern in prokaryotes[J].Gene, 2011, 488(1-2):41-45.
[16] NGUYEN S T C, FREUND H L, KASANJIAN J, et al.Function, distribution, and annotation of characterized cellulases, xylanases, and chitinases from CAZy[J].Applied Microbiology and Biotechnology, 2018, 102(4):1629-1637.
[17] 李刘若兰. 人体肠道中长双歧杆菌占据属内丰度优势的机制解析及筛选方法开发[D].无锡:江南大学, 2023.
LI-LIU R L.Mechanism analysis and screening methoddevelopment of Bifidobacterium longum occupying of the abundance dominance within thegenus in the human gut[D].Wuxi:Jiangnan University, 2023.
[18] SUN X X, YU L L, XIAO M F, et al.Exploring core fermentation microorganisms, flavor compounds, and metabolic pathways in fermented rice and wheat foods[J].Food Chemistry, 2025, 463:141019.
[19] ADE C P, BEMM F, DICKSON J M J, et al.Family 34 glycosyltransferase (GT34) genes and proteins in Pinus radiata (Radiata pine) and Pinus taeda (loblolly pine)[J].The Plant Journal, 2014, 78(2):305-318.
[20] HICKS K G, CLUNTUN A A, SCHUBERT H L, et al.Protein-metabolite interactomics of carbohydrate metabolism reveal regulation of lactate dehydrogenase[J].Science, 2023, 379(6636):996-1003.
[21] NGOUÉNAM J R, MOMO KENFACK C H, FOKO KOUAM E M, et al.Lactic acid production ability of Lactobacillus sp.from four tropical fruits using their by-products as carbon source[J].Heliyon, 2021, 7(5):e07079.
[22] WU M M, ZHAO X, SHEN Y Q, et al.Efficient simultaneous utilization of glucose and xylose from corn straw by Sphingomonas sanxanigenens NX02 to produce microbial exopolysaccharide[J].Bioresource Technology, 2021, 319:124126.
[23] LUIS A S, JIN C S, PEREIRA G V, et al.A single sulfatase is required to access colonic mucin by a gut bacterium[J].Nature, 2021, 598(7880):332-337.
[24] XU B, LIU L H, LAI S J, et al.Directed evolution of Escherichia coli nissle 1917 to utilize allulose as sole carbon source[J].Small Methods, 2024, 8(8):2301385.
[25] ZHANG W Z, ZHANG J L, ZHAO X M, et al.Efficient production of ginsenoside Rh2 from xylose by remodeling metabolism in Saccharomyces cerevisiae[J].Chemical Engineering Journal, 2024, 494:153120.
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