ISSN: 1024-2422

Journal Home

Journal Guideline

Biocatalysis and Biotransformation Q3 Unclaimed

Informa Healthcare United Kingdom

Unfortunately this journal has not been claimed yet. For this reason, some information may be unavailable.

Biocatalysis and Biotransformation is a journal indexed in SJR in Biotechnology and Biochemistry with an H index of 51. It has a price of 2395 €. It has an SJR impact factor of 0,372 and it has a best quartile of Q3. It is published in English. It has an SJR impact factor of 0,372.

Biocatalysis and Biotransformation focuses its scope in these topics and keywords: synthesis, purification, drug, dihydrogenoxidising, enantiomers, enzymatic, eutropha, evaluation, expression, family, ...

Type: Journal

Type of Copyright:

Languages: English

Open Access Policy:

Type of publications:

Publication frecuency: -

Categories: Biochemistry (Q3) Biotechnology (Q3) Catalysis (Q3)

Price

2395 €

Inmediate OA

NPD

Embargoed OA

0 €

Non OA

Metrics

0,372

SJR Impact factor

51

H Index

75

Total Docs (Last Year)

142

Total Docs (3 years)

4027

Total Refs

356

Total Cites (3 years)

140

Citable Docs (3 years)

2.3

Cites/Doc (2 years)

53.69

Ref/Doc

Comments

No comments ... Be the first to comment!

Publication speed *

Review quality *

Edition and editorial team *

Institutional email or ORCID *

* The email or ORCID field is only to validate the authenticity of the comment, the identity will not be public. .

Other journals with similar parameters

Letters in Applied Microbiology Q3
Biotechnology Letters Q3
Biotechnology and Bioprocess Engineering Q3
Acta Naturae Q3
Biotechnology and Applied Biochemistry Q3

Compare this journals

Aims and Scope

Best articles by citations

Oxidation of a mixture of 2-(R) and 2-(S)-heptanol to 2-heptanone bySaccharomyces cerevisiaein a biphasic system

Candida parapsilosisATCC 7330 can also deracemise 1-arylethanols

Rhizopus delemarLipase in Microemulsion-based Organogels: Reactivity and Rate-Limiting Study

C-2 Epimer Formation of Tetrose, Pentose and Hexose Sugars by Xylose Isomerase

Gas chromatography-mass spectrometry (GC-MS) techniques for metabolic flux analysis of the Bifido shunt pathway

Vanilla Flavour Production Through Biotransformation UsingCapsicum frutescensRoot Cultures

Chemical Modification Causes Similar Change in Dependence on Water Activity of Chymotrypsin Hydration and Catalysis in Hexane

Lipase-catalyzed regioselective protection/deprotection of hydroxyl groups of the isoflavone irilone isolated fromIris germanica

Enzymatic synthesis of a series of alkyl esters using novozyme 435 in a packed-bed, miniaturized, continuous flow reactor

Rational and Combinatorial Engineering of the Glucan Synthesizing Enzyme Amylosucrase

Enzymatic Synthesis of Hexyl Glycosides from Lactose At Low Water Activity and High Temperature Using Hyperthermostable beta-glycosidases

Enzymatic synthesis of new aromatic and aliphatic esters of flavonoids usingCandida antarcticalipase as biocatalyst

SHOW MORE ARTICLES

Lipase-mediated Resolution of Branched Chain Fatty Acids

Kinetics of Pyruvate Decarboxylase Deactivation by Benzaldehyde

Study of the Stability Of Vaccinium myrtillus Peroxidase in Reverse Micellar Systems

Enzymatic Synthesis of Thioglucosides Using Almond beta-glucosidase

Molecular engineering of a thermostable carbohydrate-binding module

Co-immobilization ofd-hydantoinase andd-carboamylase on Chitin: Application to the Synthesis of p-hydroxyphenylglycine

Aeromonas hydrophilastrains as biocatalysts for transglycosylation

Enzymatic transesterification in a solvent-free system: synthesis of sn-2 docosahexaenoyl monoacylglycerol

A toolbox approach for the rapid evaluation of multi-step enzymatic syntheses comprising a 'mix and match'E. coliexpression system with microscale experimentation

Deacylation of Cephalosporins by Lipase Catalysis and Microwave Assisted Transformation on a Solid Support

Enzymatic treatment of wool pre-treated with cetyltrimethylammonium bromide to achieve machine washability

Investigation of factors affecting biotransformation of phytosterols to 9-hydroxyandrost-4-ene-3,-17-dione based on the HP-beta-CD-resting cells reaction system