Evidence map›Paper›PMID 28644390›Full record

ArticleNanomaterials (Basel, Switzerland)2017

The Electrosome: A Surface-Displayed Enzymatic Cascade in a Biofuel Cell's Anode and a High-Density Surface-Displayed Biocathodic Enzyme.

Alon Szczupak, Dror Aizik, Sarah Moraïs, Yael Vazana, Yoav Barak, Edward A Bayer, Lital Alfonta

Abstract read
In one paragraph

Article in Nanomaterials (Basel, Switzerland), 2017. 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
–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

2 citing papers in PubMed.

  1. Review
  2. 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

7 authors.

Alon SzczupakDepartment of Life Sciences and the Ilse Katz Institute for Nanoscale Science and Technology, P.O. Box 653, 8410501 Beer-Sheva, Israel. alonszcz@post.bgu.ac.il.
Dror AizikDepartment of Life Sciences and the Ilse Katz Institute for Nanoscale Science and Technology, P.O. Box 653, 8410501 Beer-Sheva, Israel. dror12321@gmail.com.
Sarah MoraïsDepartment of Biomolecular Sciences, Weizmann Institute of Science, 234 Herzl St., P.O. Box 26, 7610001 Rehovot, Israel. sarahv@weizmann.ac.il.
Yael VazanaDepartment of Biomolecular Sciences, Weizmann Institute of Science, 234 Herzl St., P.O. Box 26, 7610001 Rehovot, Israel. yael.vazana@sial.com.
Yoav BarakDepartment of Chemical Research Support, Weizmann Institute of Science, 234 Herzl St., P.O. Box 26, 7610001 Rehovot, Israel. yoav.barak@weizmann.ac.il.
Edward A BayerDepartment of Biomolecular Sciences, Weizmann Institute of Science, 234 Herzl St., P.O. Box 26, 7610001 Rehovot, Israel. ed.bayer@weizmann.ac.il.
Lital AlfontaDepartment of Life Sciences and the Ilse Katz Institute for Nanoscale Science and Technology, P.O. Box 653, 8410501 Beer-Sheva, Israel. alfontal@bgu.ac.il.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The limitation of surface-display systems in biofuel cells to a single redox enzyme is a major drawback of hybrid biofuel cells, resulting in a low copy-number of enzymes per yeast cell and a limitation in displaying enzymatic cascades. Here we present the electrosome, a novel surface-display system based on the specific interaction between the cellulosomal scaffoldin protein and a cascade of redox enzymes that allows multiple electron-release by fuel oxidation. The electrosome is composed of two compartments: (i) a hybrid anode, which consists of dockerin-containing enzymes attached specifically to cohesin sites in the scaffoldin to assemble an ethanol oxidation cascade, and (ii) a hybrid cathode, which consists of a dockerin-containing oxygen-reducing enzyme attached in multiple copies to the cohesin-bearing scaffoldin. Each of the two compartments was designed, displayed, and tested separately. The new hybrid cell compartments displayed enhanced performance over traditional biofuel cells; in the anode, the cascade of ethanol oxidation demonstrated higher performance than a cell with just a single enzyme. In the cathode, a higher copy number per yeast cell of the oxygen-reducing enzyme copper oxidase has reduced the effect of competitive inhibition resulting from yeast oxygen consumption. This work paves the way for the assembly of more complex cascades using different enzymes and larger scaffoldins to further improve the performance of hybrid cells.

Indexed as

cellulosomecohesindockerinenzymatic cascadeshybrid biofuel cellsredox enzymesscaffoldin

Identifiers

PMID28644390
PMCPMC5535219

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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.