Evidence map›Paper›PMID 30486886›Full record

ArticleMicrobial cell factories2018

Highly efficient production of Clostridium cellulolyticum H10 D-psicose 3-epimerase in Bacillus subtilis and use of these cells to produce D-psicose.

Lingqia Su, Fan Sun, Zhanzhi Liu, Kang Zhang, Jing Wu

Open access · goldAbstract read
In one paragraph

Article in Microbial cell factories, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.1field-weighted citation impact, top 11% 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

11 citing papers in PubMed, 39 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. The Engineering, Expression, and Immobilization of Epimerases forInternational journal of molecular sciences · 2023
    Review
  5. Metabolically EngineeredFrontiers in bioengineering and biotechnology · 2022
    Article
  6. Review
  7. Engineering ofFrontiers in bioengineering and biotechnology · 2022
    Article
  8. Review
  9. Article
  10. Article
  11. Article
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

5 authors at 1 institution in 1 country.

Lingqia SuState Key Laboratory of Food Science and Technology, Jiangnan University, 1800 Lihu Avenue, Wuxi, 214122, China.
Fan SunState Key Laboratory of Food Science and Technology, Jiangnan University, 1800 Lihu Avenue, Wuxi, 214122, China.
Zhanzhi LiuState Key Laboratory of Food Science and Technology, Jiangnan University, 1800 Lihu Avenue, Wuxi, 214122, China.
Kang ZhangState Key Laboratory of Food Science and Technology, Jiangnan University, 1800 Lihu Avenue, Wuxi, 214122, China.
Jing WuState Key Laboratory of Food Science and Technology, Jiangnan University, 1800 Lihu Avenue, Wuxi, 214122, China. jingwu@jiangnan.edu.cn.ORCID http://orcid.org/0000-0002-6591-0529
Jiangnan University · CN

Funding

national first-class discipline program of Light Industry Technology and Engineering LITE2018-03National Natural Science Foundation of China 31501419National Natural Science Foundation of China 31771916National Science Fund for Distinguished Young Scholars 31425020Natural Science Foundation of Jiangsu Province BK20180082the 111 Project 111-2-06
6 · The paper itself

Abstract

backgroundD-Psicose 3-epimerase (DPEase) catalyzes the isomerization of D-fructose to the rare sugar D-psicose, which may help prevent obesity, reduce blood sugar and blood fat, and inhibit intra-abdominal fat accumulation.

resultsIn this study, the DPEase of Clostridium cellulolyticum H10 was expressed in the food-grade host Bacillus subtilis. Optimization of the culture medium during shake-flask experiments yielded a DPEase activity of 314 U/mL. The optimal medium included 20 g/L peptone, 15 g/L corn steep powder, 5 g/L glycerol, and 1 mM Ca

conclusionsThis is the first report to enhance recombinant DPEase production in B. subtilis using efficient and convenient fermentation strategy, and the DPEase yield is three times higher than the highest yield reported to date. The recombinant B. subtilis cells were further used in the efficient synthesis of D-psicose. This study provides a basis for the industrial production of D-psicose.

Indexed as

Bacillus subtilisBioreactorsCarbohydrate EpimerasesCarbonFructoseHydrogen-Ion ConcentrationIonsMetalsNitrogenRecombination, GeneticTemperatureCarbohydrate EpimerasesCarbonD-psicose 3-epimerase, Clostridium cellulolyticumFructoseIonsMetalsNitrogenpsicoseBacillus subtilisC/N ratioD-PsicoseD-Psicose 3-epimeraseHigh-cell-density fermentation

Identifiers

PMID30486886
PMCPMC6260708
OpenAlexW2902294004

What OpenQuestion holds

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LicenceCC BY
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 OpenQuestion graph.