Evidence map›Paper›PMID 42684591›Full record

ReviewWorld journal of microbiology & biotechnology2026

Bioengineering microbial cellulose synthesis pathways as biofactory for industrial-scale cellulose production: a review on current advances.

Bhargavi Pathak, Alinaj Yasin, Dibyajyoti Mahanta, Anurag Kashyap

Abstract readReview
PubMed Publisher
In one paragraph

Review in World journal of microbiology & biotechnology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Bhargavi Pathak *Department of Plant Pathology, Assam Agricultural University, Jorhat, Assam, 785013, India.ORCID http://orcid.org/0009-0007-5502-9379
Alinaj Yasin *Department of Plant Pathology, Assam Agricultural University, Jorhat, Assam, 785013, India.ORCID http://orcid.org/0000-0003-2753-1023
Dibyajyoti Mahanta *Department of Plant Pathology, Assam Agricultural University, Jorhat, Assam, 785013, India.ORCID http://orcid.org/0009-0000-4416-5833
Anurag KashyapDepartment of Plant Pathology, Assam Agricultural University, Jorhat, Assam, 785013, India. anurag.kashyap@aau.ac.in.ORCID http://orcid.org/0000-0003-2622-8209

Funding

Department of Science and Technology, Govt. of India under Technology Development Programme DST Project Ref. No: TPN / 77754
6 · The paper itself

Abstract

Microbial cellulose (MC) is a natural biopolymer distinguished by its chemical purity, nanofibrillar architecture, eco-friendliness, biodegradability, and mechanical properties. These distinctive features of MC have expanded the potential applications across diverse fields. However, its transition from laboratory-scale production to industrial manufacturing remains constrained by its low productivity, high production costs, genetic instability of the cellulose-producing strains, accumulation of inhibitory by-products, and inadequate oxygen supply during the fermentation process. These limitations are further complicated by poor standardization of the relationship between the engineered biosynthetic pathways and the resulting physicochemical properties of cellulose. Hence, this review critically examines MC biosynthesis pathways across bacteria, algae, and oomycetes, with particular emphasis on the bacteria as the most advanced biofactory for MC production. Recent advances in metabolic engineering, genome editing, and synthetic biology have opened unprecedented avenues to enhance large-scale cellulose productivity by optimizing precursor pathways, suppressing byproduct formation, engineering cyclic-di-GMP regulatory networks, efficient oxygen utilization, and developing synthetic biology toolkits. Finally, we identify key research priorities including development of genetically stable microbial strains, improved oxygen-management strategies, and integrated strain-process engineering required to translate MC production from laboratory to commercially viable biofactories. In parallel, innovations in technology like advanced fermentation strategy and bioreactor designs are the crucial determinants for accelerating MC production, bridging the gaps between experimental conditions and commercial implementation. Altogether, these advancements will lay the foundation and pave the way for developing efficient cellulose biofactories to meet the increasing demand for high-quality and sustainable biomaterials, fostering the transition towards a resource-efficient, eco-friendly future.

Indexed as

BioengineeringBiosynthetic PathwaysCelluloseIndustrial MicrobiologyMetabolic EngineeringBacteriaFermentationSynthetic BiologyCelluloseBcs operonBioengineeringBiofactoryBiopolymerMicrobial cellulose

Identifiers

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.