2017
DOI: 10.1007/10_2017_6
|View full text |Cite
|
Sign up to set email alerts
|

Biotechnological and Biochemical Utilization of Lignin

Abstract: This chapter provides an overview of the biosynthesis and structure of lignin. Moreover, examples of the commercial use of lignin and its promising future implementation are briefly described. Many applications are still hampered by the properties of technical lignins. Thus, the major challenge is the conversion of lignins into suitable building blocks or aromatics in order to open up new avenues for the usage of this renewable raw material. This chapter focuses on details about natural lignin degradation by f… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
4
1

Citation Types

0
8
0

Year Published

2017
2017
2023
2023

Publication Types

Select...
6
2
1

Relationship

0
9

Authors

Journals

citations
Cited by 11 publications
(8 citation statements)
references
References 198 publications
0
8
0
Order By: Relevance
“…During the following reaction cycle, Compound I is reduced by oxidation of two substrate molecules to the state during enzyme resting state in two sequential steps with Compound II as intermediate. However, the existence of Compound II has not been confirmed universally for all DyP-type peroxidases [17]. In the presence of excessive hydrogen peroxide suicide inhibition was observed for different DyPs [18,19].…”
Section: Introductionmentioning
confidence: 94%
See 1 more Smart Citation
“…During the following reaction cycle, Compound I is reduced by oxidation of two substrate molecules to the state during enzyme resting state in two sequential steps with Compound II as intermediate. However, the existence of Compound II has not been confirmed universally for all DyP-type peroxidases [17]. In the presence of excessive hydrogen peroxide suicide inhibition was observed for different DyPs [18,19].…”
Section: Introductionmentioning
confidence: 94%
“…An increase of the hydrogen peroxide concentration led to a continuous activity decrease. Suicide inhibition in the presence of excess hydrogen peroxide is well known for classical peroxidases as a result of the formation of an inactive oxidative state (Compound III) by reaction of H 2 O 2 and Compound II [20,21], even if the existence of Compound II has not been confirmed for DyP-type peroxidases universally [17]. However, inhibition of other DyPs in the presence of higher hydrogen peroxide concentrations has been reported [18,19].…”
Section: Biochemical Characterization Of Psapoxmentioning
confidence: 99%
“…Faced with growing consumer demand for bio-based or natural products and the need to become less dependent on fossil resources, industry is turning to eco-friendlier products and processes. In this context, lignin and related chemicals (e.g., lignans, phenolic acids) appear as a valuable source of sustainable aromatic building blocks [1,2]. Indeed, p-hydroxycinnamic acids and their derivatives can be readily extracted from different biomasses and be further (chemo-)enzymatically modified [3][4][5][6] to provide them with physicochemical and biological properties of interest in various fields, such as antioxidants [7][8][9] and anti-UV compounds [10][11][12].…”
Section: Introductionmentioning
confidence: 99%
“…Lignin is a natural biopolymer with a number of beneficial properties including biodegradability and biocompatibility [10,11,12,13,14]. Recently, the use of lignin is increasing as a sustainable polymer for preparing carbon fibers [15], biofuels, bioplastics and controlled release carriers [16,17,18,19,20,21]. Due to the existence of different functional groups in the lignin structure such as phenolic, hydroxyl and carboxyl groups, lignin can be chemically modified to enhance drug delivery and to control drug release [22,23,24].…”
Section: Introductionmentioning
confidence: 99%