Evidence map›Paper›PMID 25679965›Full record

ArticlePloS one2015

Comparative transcriptome analysis reveals that lactose acts as an inducer and provides proper carbon sources for enhancing exopolysaccharide yield in the deep-sea bacterium Zunongwangia profunda SM-A87.

Qi-Long Qin, Yi Li, Mei-Ling Sun, Jin-Cheng Rong, Sheng-Bo Liu, Xiu-Lan Chen, Hai-Nan Su, Bai-Cheng Zhou, Bin-Bin Xie, Yu-Zhong Zhang and 1 more

Open access · goldAbstract readComparative Study
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.2field-weighted citation impact, top 44% of its field
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

2 citing papers in PubMed, 5 citations in OpenAlex.

  1. High-Density Fermentation ofFoods (Basel, Switzerland) · 2024
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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

11 authors at 2 institutions in 1 country.

Qi-Long QinState Key Laboratory of Microbial Technology, Shandong University, Jinan 250100, China; Marine Biotechnology Research Center, Shandong University, Jinan 250100, China.
Yi LiState Key Laboratory of Microbial Technology, Shandong University, Jinan 250100, China; Marine Biotechnology Research Center, Shandong University, Jinan 250100, China.
Mei-Ling SunState Key Laboratory of Microbial Technology, Shandong University, Jinan 250100, China; Marine Biotechnology Research Center, Shandong University, Jinan 250100, China.
Jin-Cheng RongState Key Laboratory of Microbial Technology, Shandong University, Jinan 250100, China; Marine Biotechnology Research Center, Shandong University, Jinan 250100, China.
Sheng-Bo LiuState Key Laboratory of Microbial Technology, Shandong University, Jinan 250100, China; Marine Biotechnology Research Center, Shandong University, Jinan 250100, China.
Xiu-Lan ChenState Key Laboratory of Microbial Technology, Shandong University, Jinan 250100, China; Marine Biotechnology Research Center, Shandong University, Jinan 250100, China.
Hai-Nan SuState Key Laboratory of Microbial Technology, Shandong University, Jinan 250100, China; Marine Biotechnology Research Center, Shandong University, Jinan 250100, China.
Bai-Cheng ZhouMarine Biotechnology Research Center, Shandong University, Jinan 250100, China.
Bin-Bin XieState Key Laboratory of Microbial Technology, Shandong University, Jinan 250100, China; Marine Biotechnology Research Center, Shandong University, Jinan 250100, China.
Yu-Zhong ZhangState Key Laboratory of Microbial Technology, Shandong University, Jinan 250100, China; Marine Biotechnology Research Center, Shandong University, Jinan 250100, China.
Xi-Ying ZhangState Key Laboratory of Microbial Technology, Shandong University, Jinan 250100, China; Marine Biotechnology Research Center, Shandong University, Jinan 250100, China.
State Key Laboratory of Microbial TechnologyShandong University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Many marine bacteria secrete exopolysaccharides (EPSs) that have important ecological and physiological functions. Numerous nutritional and environmental factors influence bacterial EPS production. However, the regulatory mechanisms of EPS production are poorly understood. The deep-sea Bacteroidetes bacterium Zunongwangia profunda SM-A87 can produce high quantities of EPS, and its EPS production is enhanced significantly by lactose. Here, we studied the reasons behind the significant advantage that lactose has over other carbon sources in EPS production in SM-A87. RNA-seq technologies were used to study lactose-regulated genes in SM-A87. The expression level of genes within the EPS gene cluster was up-regulated when lactose was added. Supplement of lactose also influenced the expression of genes located outside the EPS gene cluster that are also involved in EPS biosynthesis. The major glycosyl components of SM-A87 EPS are mannose, glucose and galactose. Genomic metabolic pathway analyses showed that the EPS precursor GDP-mannose can be synthesized from glucose, while the precursor UDP-glucose must be synthesized from galactose. Lactose can provide glucose and galactose simultaneously and prevent glucose inhibition. Lactose can also greatly stimulate the growth of SM-A87. Taken together, lactose acts not only as an inducer but also as a carbohydrate source for EPS production. This research broadens our knowledge of the regulation of EPS production in marine bacteria.

Indexed as

Gene Expression ProfilingCulture MediaFlavobacteriaceaeLactoseMultigene FamilyPolysaccharides, BacterialUp-RegulationCulture MediaLactosePolysaccharides, Bacterial

Identifiers

PMID25679965
PMCPMC4332637
OpenAlexW1967636499

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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 OpenQuestion graph.