Bioengineering Caulobacter vibrioides for Xylanase Applications in the Bakery Industry

The present study investigated the impact of genetic engineering strategies to produce a cell-free xylanase for applications in the baking industry. The <i>xynA1</i> gene from the nonpathogenic bacterium <i>Caulobacter vibrioides</i> was integrated into the pAS22 vector with a xylose-inducible promoter and introduced back into the bacteria, resulting in the creation of the BS-<i>xynA1</i>. This construct exhibited substantial secreted xylanase 1 (XynA1) activity, reaching 17.22 U/mL, and a specific activity of 278.64 U/mg after an 18 h growth period with 0.3% (<i>v</i>/<i>v</i>) xylose plus 0.2% (<i>w</i>/<i>v</i>) corn straw. RT-qPCR analysis confirmed that higher xylanase activity in <i>C. vibrioides</i> cells was correlated with increased transcription of the <i>xynA1</i> gene in the induction medium. Moreover, BS-<i>xynA1</i> cells coexpress other enzymes, including xylanase 2 (XynA2), cellulase, pectinase, α-amylase, β-glucosidase, β-xylosidase, and α-L-arabinosidase, at low levels (≤2 U/mL). In vitro comparison of cell-free xylanases from BS-<i>xynA1</i> with three commercially available xylanase-containing mixtures commonly utilized in baking protocols revealed its superior specific activity (163.4 U/mg) across a broad temperature range (30-100 °C), with optimal performance at 50 °C. In practical baking tests, the addition of cell-free XynA1 led to a reduction in dough kneading time and increase in bread height compared to those of the control. Notably, the incorporation of XynA1 resulted in enhanced alveolar structure formation within the bread crumb. Specifically, the following changes were observed in the mass parameters compared to those of the control: an increase in extensibility, elasticity, and deformation energy, and subsequent improvements in strength. Additionally, XynA1 addition led to a reduction in toughness and toughness/elasticity index, indicating a reduction in the mass stiffness of the enzyme-treated bread. To date, this is the first successful application of recombinant XynA1 from <i>C. vibrioides</i> in biotechnological processes related to baking, underscoring the potential and prospects in the food industry.

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Journal
Microorganisms
Published
2025-10-15
DOI
https://doi.org/10.3390/microorganisms13102367
Citations
1
Primary Topic
Biofuel production and bioconversion
Type
article
Field-Weighted Citation Impact
0.67

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article

Bioengineering Caulobacter vibrioides for Xylanase Applications in the Bakery Industry

José Luis da Conceição Silva, Rinaldo Ferreira Gandra, Marina Kimiko Kadowaki, Bruna Simioni et al.
1 citations
Microorganisms
Biofuel production and bioconversion
0.67
article

Bioengineering Caulobacter vibrioides for Xylanase Applications in the Bakery Industry

José Luis da Conceição Silva, Rinaldo Ferreira Gandra, Marina Kimiko Kadowaki, Bruna Simioni, Alexandre Maller, Rita de Cássia Garcia Simão, Adriano Fávero, Paula Maria Carneiro Rocha
article en
1 citations

Abstract

The present study investigated the impact of genetic engineering strategies to produce a cell-free xylanase for applications in the baking industry. The <i>xynA1</i> gene from the nonpathogenic bacterium <i>Caulobacter vibrioides</i> was integrated into the pAS22 vector with a xylose-inducible promoter and introduced back into the bacteria, resulting in the creation of the BS-<i>xynA1</i>. This construct exhibited substantial secreted xylanase 1 (XynA1) activity, reaching 17.22 U/mL, and a specific activity of 278.64 U/mg after an 18 h growth period with 0.3% (<i>v</i>/<i>v</i>) xylose plus 0.2% (<i>w</i>/<i>v</i>) corn straw. RT-qPCR analysis confirmed that higher xylanase activity in <i>C. vibrioides</i> cells was correlated with increased transcription of the <i>xynA1</i> gene in the induction medium. Moreover, BS-<i>xynA1</i> cells coexpress other enzymes, including xylanase 2 (XynA2), cellulase, pectinase, α-amylase, β-glucosidase, β-xylosidase, and α-L-arabinosidase, at low levels (≤2 U/mL). In vitro comparison of cell-free xylanases from BS-<i>xynA1</i> with three commercially available xylanase-containing mixtures commonly utilized in baking protocols revealed its superior specific activity (163.4 U/mg) across a broad temperature range (30-100 °C), with optimal performance at 50 °C. In practical baking tests, the addition of cell-free XynA1 led to a reduction in dough kneading time and increase in bread height compared to those of the control. Notably, the incorporation of XynA1 resulted in enhanced alveolar structure formation within the bread crumb. Specifically, the following changes were observed in the mass parameters compared to those of the control: an increase in extensibility, elasticity, and deformation energy, and subsequent improvements in strength. Additionally, XynA1 addition led to a reduction in toughness and toughness/elasticity index, indicating a reduction in the mass stiffness of the enzyme-treated bread. To date, this is the first successful application of recombinant XynA1 from <i>C. vibrioides</i> in biotechnological processes related to baking, underscoring the potential and prospects in the food industry.

MicroorganismsVol. 13(10)
Universidade Estadual do Oeste do Paraná (BR)
Secretário de Ciência, Tecnologia e Ensino Superior, Governo do Estado de Parana
Openalex Percentile: Top 26%
Biofuel production and bioconversion
0.67
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