Evidence map›Paper›PMID 42411005›Full record

ReviewJournal of basic microbiology2026

Microbial Enzyme Production: Critical Bottlenecks and Integrated Engineering Solutions.

Poulami Maji, Anannya Sengupta, Paramita Ghosh, Prashant Shukla

Abstract readReview
In one paragraph

Review in Journal of basic microbiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Poulami MajiDepartment of Biotechnology, Brainware University, Barasat, West Bengal, India.
Anannya SenguptaDepartment of Biotechnology, Brainware University, Barasat, West Bengal, India.
Paramita GhoshDepartment of Biotechnology, Brainware University, Barasat, West Bengal, India.
Prashant ShuklaDepartment of Biotechnology, Brainware University, Barasat, West Bengal, India.ORCID https://orcid.org/0000-0003-0350-0302

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Microbial enzymes are central to numerous industrial applications, yet their large-scale production remains constrained by persistent biological and process-level limitations. These include restricted secretion capacity, insufficient operational stability, scale-up inefficiencies, and downstream processing costs that can account for 45-65% of total manufacturing expenses. This review critically examines integrated genetic, physiological, and bioprocess engineering strategies developed to overcome these interconnected bottlenecks. Comparative analysis across major enzyme classes-cellulases, proteases, lipases, and amylases-reveals both universal constraints and enzyme-specific production challenges. Quantitative benchmarks indicate that multiplex genome engineering typically delivers 3-8-fold productivity improvements in optimized strains, while adaptive laboratory evolution enhances industrial robustness by 15-30%. Process intensification and continuous production approaches reduce processing times by 40-55%, albeit with increased capital requirements, and immobilization strategies enable 50-200 operational cycles with 65-85% retention of native activity. By synthesizing advances in strain engineering, secretion optimization, fermentation design, enzyme stabilization, and downstream integration within a techno-economic framework, this review highlights how coordinated interventions yield multiplicative gains over isolated strategies. Key future directions include systems-level characterization of secretion limits, AI-assisted enzyme stability engineering, and integrated manufacturing platforms. Collectively, these insights provide practical guidance for translating laboratory advances into economically viable microbial enzyme production systems.

Indexed as

BacteriaEnzymesIndustrial MicrobiologyMetabolic EngineeringBioreactorsEnzymes, ImmobilizedEnzyme StabilityFermentationGenetic EngineeringEnzymesEnzymes, Immobilizedbioprocess intensificationenzyme immobilizationhigh‐cell‐density fermentationindustrial biocatalysismicrobial enzyme productionscale‐upsecretion capacitystrain engineering

Identifiers

PMID42411005
PMCPMC13377295

What Socratic holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.